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 6194223 6194223 + Missense_Mutation SNP G G A TCGA-OR-A5J5-01A-11D-A29I-10 TCGA-OR-A5J5-10A-01D-A29L-10 g.chr1:6194223G>A c.3109C>T c.(3109-3111)Cgg>Tgg p.R1037W ACC 1 6196856 6196856 + Silent SNP G G A TCGA-OR-A5KB-01A-11D-A30A-10 TCGA-OR-A5KB-11A-11D-A30A-10 g.chr1:6196856G>A c.2506C>T c.(2506-2508)Ctg>Ttg p.L836L ACC 1 6204158 6204158 + Missense_Mutation SNP G G T TCGA-OR-A5J8-01A-11D-A29I-10 TCGA-OR-A5J8-10A-01D-A29L-10 g.chr1:6204158G>T c.1860C>A c.(1858-1860)gaC>gaA p.D620E BLCA 1 6169928 6169928 + Silent SNP G G A TCGA-4Z-AA7Q-01A-11D-A391-08 TCGA-4Z-AA7Q-10A-01D-A394-08 g.chr1:6169928G>A c.5505C>T c.(5503-5505)ctC>ctT p.L1835L BLCA 1 6169989 6169989 + Missense_Mutation SNP G G A TCGA-DK-A3X2-01A-11D-A22Z-08 TCGA-DK-A3X2-10A-01D-A22Z-08 g.chr1:6169989G>A c.5444C>T c.(5443-5445)aCg>aTg p.T1815M BLCA 1 6170532 6170532 + Silent SNP G G C TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chr1:6170532G>C c.5304C>G c.(5302-5304)ctC>ctG p.L1768L BLCA 1 6173059 6173059 + Splice_Site SNP C C G TCGA-DK-A1A3-01A-11D-A13W-08 TCGA-DK-A1A3-10A-01D-A13W-08 g.chr1:6173059C>G c.e34-1 BLCA 1 6173060 6173060 + Splice_Site SNP T T C TCGA-DK-AA6L-01A-11D-A391-08 TCGA-DK-AA6L-10A-01D-A394-08 g.chr1:6173060T>C c.e34-2 BLCA 1 6181183 6181183 + Missense_Mutation SNP G G C TCGA-XF-A9T3-01A-11D-A42E-08 TCGA-XF-A9T3-10A-01D-A42H-08 g.chr1:6181183G>C c.4894C>G c.(4894-4896)Ccg>Gcg p.P1632A BLCA 1 6181225 6181225 + Nonsense_Mutation SNP G G A TCGA-FD-A3SS-01A-12D-A22Z-08 TCGA-FD-A3SS-10A-01D-A22Z-08 g.chr1:6181225G>A c.4852C>T c.(4852-4854)Cga>Tga p.R1618* BLCA 1 6181234 6181234 + Missense_Mutation SNP C C T TCGA-FD-A6TG-01A-11D-A32B-08 TCGA-FD-A6TG-10A-01D-A329-08 g.chr1:6181234C>T c.4843G>A c.(4843-4845)Gag>Aag p.E1615K BLCA 1 6181594 6181594 + Missense_Mutation SNP T T A TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr1:6181594T>A c.4739A>T c.(4738-4740)gAc>gTc p.D1580V BLCA 1 6184081 6184081 + Silent SNP C C T TCGA-E5-A4U1-01A-11D-A31L-08 TCGA-E5-A4U1-10B-01D-A31J-08 g.chr1:6184081C>T c.4626G>A c.(4624-4626)gtG>gtA p.V1542V BLCA 1 6184104 6184104 + Missense_Mutation SNP C C T TCGA-E5-A4U1-01A-11D-A31L-08 TCGA-E5-A4U1-10B-01D-A31J-08 g.chr1:6184104C>T c.4603G>A c.(4603-4605)Gag>Aag p.E1535K BLCA 1 6184141 6184141 + Silent SNP C C A TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr1:6184141C>A c.4566G>T c.(4564-4566)ggG>ggT p.G1522G BLCA 1 6184141 6184141 + Silent SNP C C A TCGA-E5-A4U1-01A-11D-A31L-08 TCGA-E5-A4U1-10B-01D-A31J-08 g.chr1:6184141C>A c.4566G>T c.(4564-4566)ggG>ggT p.G1522G BLCA 1 6184142 6184142 + Missense_Mutation SNP C C A TCGA-E5-A4U1-01A-11D-A31L-08 TCGA-E5-A4U1-10B-01D-A31J-08 g.chr1:6184142C>A c.4565G>T c.(4564-4566)gGg>gTg p.G1522V BLCA 1 6185886 6185886 + Missense_Mutation SNP C C T TCGA-E5-A4U1-01A-11D-A31L-08 TCGA-E5-A4U1-10B-01D-A31J-08 g.chr1:6185886C>T c.4111G>A c.(4111-4113)Gaa>Aaa p.E1371K BLCA 1 6186675 6186675 + Silent SNP G G A TCGA-ZF-AA51-01A-21D-A391-08 TCGA-ZF-AA51-10A-01D-A394-08 g.chr1:6186675G>A c.4035C>T c.(4033-4035)atC>atT p.I1345I BLCA 1 6188917 6188917 + Silent SNP G G C TCGA-GD-A3OQ-01A-32D-A21Z-08 TCGA-GD-A3OQ-10A-01D-A21Z-08 g.chr1:6188917G>C c.3600C>G c.(3598-3600)ctC>ctG p.L1200L BLCA 1 6189100 6189100 + Silent SNP C C T TCGA-BT-A2LB-01A-11D-A18F-08 TCGA-BT-A2LB-10A-01D-A18F-08 g.chr1:6189100C>T c.3417G>A c.(3415-3417)caG>caA p.Q1139Q BLCA 1 6189110 6189110 + Missense_Mutation SNP C C T TCGA-2F-A9KP-01A-11D-A38G-08 TCGA-2F-A9KP-10A-01D-A38J-08 g.chr1:6189110C>T c.3407G>A c.(3406-3408)cGc>cAc p.R1136H BLCA 1 6191772 6191772 + Missense_Mutation SNP C C G TCGA-UY-A8OB-01A-12D-A42E-08 TCGA-UY-A8OB-11A-12D-A42H-08 g.chr1:6191772C>G c.3181G>C c.(3181-3183)Gag>Cag p.E1061Q BLCA 1 6195343 6195343 + Silent SNP G G A TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr1:6195343G>A c.2817C>T c.(2815-2817)aaC>aaT p.N939N BLCA 1 6196893 6196893 + Silent SNP G G C TCGA-GV-A3JX-01A-11D-A20D-08 TCGA-GV-A3JX-10A-01D-A20D-08 g.chr1:6196893G>C c.2469C>G c.(2467-2469)ctC>ctG p.L823L BLCA 1 6196898 6196898 + Silent SNP G G A TCGA-UY-A9PH-01A-11D-A38G-08 TCGA-UY-A9PH-10A-01D-A38J-08 g.chr1:6196898G>A c.2464C>T c.(2464-2466)Ctg>Ttg p.L822L BLCA 1 6202244 6202244 + Missense_Mutation SNP C C T TCGA-KQ-A41S-01A-12D-A339-08 TCGA-KQ-A41S-10C-01D-A339-08 g.chr1:6202244C>T c.2380G>A c.(2380-2382)Gag>Aag p.E794K BLCA 1 6202292 6202292 + Missense_Mutation SNP C C T TCGA-XF-AAMQ-01A-11D-A42E-08 TCGA-XF-AAMQ-10A-01D-A42H-08 g.chr1:6202292C>T c.2332G>A c.(2332-2334)Gtc>Atc p.V778I BLCA 1 6202308 6202308 + Silent SNP C C T TCGA-4Z-AA7O-01A-31D-A391-08 TCGA-4Z-AA7O-10A-01D-A394-08 g.chr1:6202308C>T c.2316G>A c.(2314-2316)gcG>gcA p.A772A BLCA 1 6202515 6202515 + Missense_Mutation SNP T T C TCGA-4Z-AA84-01A-11D-A391-08 TCGA-4Z-AA84-10A-01D-A394-08 g.chr1:6202515T>C c.2194A>G c.(2194-2196)Acg>Gcg p.T732A BLCA 1 6206323 6206323 + Missense_Mutation SNP C C T TCGA-G2-A2EJ-01A-11D-A17V-08 TCGA-G2-A2EJ-10A-01D-A17V-08 g.chr1:6206323C>T c.1751G>A c.(1750-1752)cGc>cAc p.R584H BLCA 1 6206806 6206806 + Silent SNP C C T TCGA-C4-A0EZ-01A-21D-A10S-08 TCGA-C4-A0EZ-10A-01D-A10S-08 g.chr1:6206806C>T c.1509G>A c.(1507-1509)ctG>ctA p.L503L BLCA 1 6208929 6208929 + Silent SNP G G A TCGA-DK-AA75-01A-11D-A391-08 TCGA-DK-AA75-10A-01D-A394-08 g.chr1:6208929G>A c.1368C>T c.(1366-1368)ctC>ctT p.L456L BLCA 1 6208929 6208929 + Silent SNP G G A TCGA-E7-A7XN-01A-11D-A34U-08 TCGA-E7-A7XN-10A-01D-A34X-08 g.chr1:6208929G>A c.1368C>T c.(1366-1368)ctC>ctT p.L456L BLCA 1 6214906 6214906 + Missense_Mutation SNP C C T TCGA-DK-A3IK-01A-32D-A21A-08 TCGA-DK-A3IK-10A-01D-A21A-08 g.chr1:6214906C>T c.559G>A c.(559-561)Gtc>Atc p.V187I BLCA 1 6215671 6215671 + Missense_Mutation SNP C C T TCGA-GU-A763-01A-11D-A32B-08 TCGA-GU-A763-10A-01D-A329-08 g.chr1:6215671C>T c.494G>A c.(493-495)aGc>aAc p.S165N BLCA 1 6219573 6219573 + Silent SNP C C T TCGA-DK-A3IM-01A-11D-A20D-08 TCGA-DK-A3IM-10A-01D-A20D-08 g.chr1:6219573C>T c.210G>A c.(208-210)ggG>ggA p.G70G BRCA 1 6166465 6166465 + Silent SNP G G C TCGA-AC-A5EH-01A-11D-A28B-09 TCGA-AC-A5EH-10A-01D-A28E-09 g.chr1:6166465G>C c.5847C>G c.(5845-5847)ccC>ccG p.P1949P BRCA 1 6166527 6166527 + Missense_Mutation SNP G G A TCGA-EW-A3U0-01A-11D-A228-09 TCGA-EW-A3U0-10A-01D-A22A-09 g.chr1:6166527G>A c.5785C>T c.(5785-5787)Ccc>Tcc p.P1929S BRCA 1 6169975 6169975 + Missense_Mutation SNP G G A TCGA-D8-A1JK-01A-11D-A13L-09 TCGA-D8-A1JK-10A-01D-A13O-09 g.chr1:6169975G>A c.5458C>T c.(5458-5460)Cac>Tac p.H1820Y BRCA 1 6172237 6172237 + Missense_Mutation SNP G G C TCGA-AO-A03M-01B-11D-A10M-09 TCGA-AO-A03M-10A-01D-A10M-09 g.chr1:6172237G>C c.5103C>G c.(5101-5103)ttC>ttG p.F1701L BRCA 1 6172263 6172263 + Missense_Mutation SNP T T C TCGA-GM-A2D9-01A-11D-A18P-09 TCGA-GM-A2D9-11A-42D-A18P-09 g.chr1:6172263T>C c.5077A>G c.(5077-5079)Aag>Gag p.K1693E BRCA 1 6181297 6181297 + Splice_Site SNP C C T TCGA-BH-A0HA-01A-11D-A12Q-09 TCGA-BH-A0HA-11A-31D-A12Q-09 g.chr1:6181297C>T c.4780G>A c.(4780-4782)Gcc>Acc p.A1594T BRCA 1 6181593 6181593 + Missense_Mutation SNP G G T TCGA-AR-A256-01A-11D-A167-09 TCGA-AR-A256-10A-01D-A167-09 g.chr1:6181593G>T c.4740C>A c.(4738-4740)gaC>gaA p.D1580E BRCA 1 6185196 6185196 + Missense_Mutation SNP A A C TCGA-E2-A15I-01A-21D-A135-09 TCGA-E2-A15I-11A-32D-A135-09 g.chr1:6185196A>C c.4358T>G c.(4357-4359)gTg>gGg p.V1453G BRCA 1 6191719 6191719 + Silent SNP G G T TCGA-A7-A426-01A-22D-A243-09 TCGA-A7-A426-10A-01D-A243-09 g.chr1:6191719G>T c.3234C>A c.(3232-3234)ctC>ctA p.L1078L BRCA 1 6191787 6191787 + Missense_Mutation SNP G G T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr1:6191787G>T c.3166C>A c.(3166-3168)Ctg>Atg p.L1056M BRCA 1 6194863 6194863 + Frame_Shift_Del DEL C C - TCGA-D8-A1JK-01A-11D-A13L-09 TCGA-D8-A1JK-10A-01D-A13O-09 g.chr1:6194863delC c.2927delG c.(2926-2928)ggcfs p.G977fs BRCA 1 6194863 6194863 + Missense_Mutation SNP C C T TCGA-BH-A0B6-01A-11D-A19Y-09 TCGA-BH-A0B6-10A-01D-A19Y-09 g.chr1:6194863C>T c.2927G>A c.(2926-2928)gGc>gAc p.G976D BRCA 1 6195315 6195315 + Missense_Mutation SNP G G A TCGA-E2-A10C-01A-21D-A10M-09 TCGA-E2-A10C-10A-01D-A10M-09 g.chr1:6195315G>A c.2845C>T c.(2845-2847)Cgg>Tgg p.R949W BRCA 1 6202309 6202309 + Missense_Mutation SNP G G A TCGA-E2-A15J-01A-11D-A12Q-09 TCGA-E2-A15J-10A-01D-A12Q-09 g.chr1:6202309G>A c.2315C>T c.(2314-2316)gCg>gTg p.A772V BRCA 1 6202326 6202326 + Silent SNP G G A TCGA-A2-A0EY-01A-11W-A050-09 TCGA-A2-A0EY-10A-01W-A055-09 g.chr1:6202326G>A c.2298C>T c.(2296-2298)cgC>cgT p.R766R BRCA 1 6204082 6204082 + Splice_Site SNP A A C TCGA-A2-A0T5-01A-21D-A099-09 TCGA-A2-A0T5-10A-01D-A099-09 g.chr1:6204082A>C c.e12+1 BRCA 1 6206325 6206325 + Silent SNP G G A TCGA-AN-A0XR-01A-11D-A10G-09 TCGA-AN-A0XR-10A-01D-A117-09 g.chr1:6206325G>A c.1749C>T c.(1747-1749)taC>taT p.Y583Y BRCA 1 6211099 6211099 + Missense_Mutation SNP C C A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr1:6211099C>A c.987G>T c.(985-987)aaG>aaT p.K329N BRCA 1 6214772 6214773 + Frame_Shift_Ins INS - - G TCGA-BH-A0DZ-01A-11W-A019-09 TCGA-BH-A0DZ-10A-01W-A021-09 g.chr1:6214772_6214773insG c.692_693insC c.(691-693)ccgfs p.P231fs BRCA 1 6215763 6215763 + Silent SNP C C T TCGA-BH-A0HP-01A-12D-A099-09 TCGA-BH-A0HP-10A-01D-A099-09 g.chr1:6215763C>T c.402G>A c.(400-402)tcG>tcA p.S134S CESC 1 6169958 6169958 + Silent SNP G G C TCGA-IR-A3LA-01A-11D-A22X-09 TCGA-IR-A3LA-10A-01D-A22X-09 g.chr1:6169958G>C c.5475C>G c.(5473-5475)ctC>ctG p.L1825L CESC 1 6170487 6170487 + Silent SNP C C T TCGA-DS-A7WH-01A-22D-A351-09 TCGA-DS-A7WH-10A-01D-A351-09 g.chr1:6170487C>T c.5349G>A c.(5347-5349)gaG>gaA p.E1783E CESC 1 6202574 6202574 + Missense_Mutation SNP C C T TCGA-EK-A2RN-01A-12D-A20U-09 TCGA-EK-A2RN-10A-01D-A20U-09 g.chr1:6202574C>T c.2135G>A c.(2134-2136)cGc>cAc p.R712H CESC 1 6211203 6211203 + Missense_Mutation SNP C C T TCGA-JX-A3Q0-01A-11D-A21Q-09 TCGA-JX-A3Q0-10A-01D-A21Q-09 g.chr1:6211203C>T c.883G>A c.(883-885)Gag>Aag p.E295K CESC 1 6214792 6214792 + Missense_Mutation SNP G G A TCGA-IR-A3LI-01A-11D-A20U-09 TCGA-IR-A3LI-10A-01D-A20U-09 g.chr1:6214792G>A c.673C>T c.(673-675)Ccg>Tcg p.P225S CESC 1 6214952 6214952 + Silent SNP G G C TCGA-DR-A0ZM-01A-12D-A10S-08 TCGA-DR-A0ZM-10A-01D-A10S-08 g.chr1:6214952G>C c.513C>G c.(511-513)ctC>ctG p.L171L CESC 1 6228322 6228323 + Frame_Shift_Ins INS - - CA TCGA-IR-A3LB-01A-11D-A243-09 TCGA-IR-A3LB-10A-01D-A243-09 g.chr1:6228322_6228323insCA c.94_95insTG c.(94-96)ggtfs p.G32fs CHOL 1 6188616 6188616 + Missense_Mutation SNP A A G TCGA-W5-AA2W-01A-11D-A417-09 TCGA-W5-AA2W-10A-01D-A41A-09 g.chr1:6188616A>G c.3673T>C c.(3673-3675)Tcc>Ccc p.S1225P CHOL 1 6194805 6194805 + Missense_Mutation SNP G G T TCGA-WD-A7RX-01A-12D-A417-09 TCGA-WD-A7RX-10A-01D-A41A-09 g.chr1:6194805G>T c.2985C>A c.(2983-2985)caC>caA p.H995Q COAD 1 6166720 6166720 + Missense_Mutation SNP G G T TCGA-F4-6703-01A-11D-1835-10 TCGA-F4-6703-10A-01D-1835-10 g.chr1:6166720G>T c.5698C>A c.(5698-5700)Ctg>Atg p.L1900M COAD 1 6166758 6166758 + Frame_Shift_Del DEL G G - TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr1:6166758delG c.5660delC c.(5659-5661)ccgfs p.P1887fs COAD 1 6171834 6171834 + Splice_Site SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr1:6171834C>T c.e36+1 COAD 1 6181217 6181217 + Silent SNP C C T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr1:6181217C>T c.4860G>A c.(4858-4860)gaG>gaA p.E1620E COAD 1 6181243 6181243 + Missense_Mutation SNP C C T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr1:6181243C>T c.4834G>A c.(4834-4836)Gcc>Acc p.A1612T COAD 1 6184072 6184072 + Silent SNP C C T TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chr1:6184072C>T c.4635G>A c.(4633-4635)tcG>tcA p.S1545S COAD 1 6184144 6184144 + Silent SNP G G A TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr1:6184144G>A c.4563C>T c.(4561-4563)aaC>aaT p.N1521N COAD 1 6184675 6184675 + Missense_Mutation SNP C C T TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr1:6184675C>T c.4441G>A c.(4441-4443)Gat>Aat p.D1481N COAD 1 6185218 6185218 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr1:6185218C>T c.4336G>A c.(4336-4338)Gcc>Acc p.A1446T COAD 1 6186793 6186793 + Missense_Mutation SNP C C A TCGA-G4-6307-01A-11D-1719-10 TCGA-G4-6307-10A-01D-1720-10 g.chr1:6186793C>A c.3917G>T c.(3916-3918)cGg>cTg p.R1306L COAD 1 6188196 6188196 + Silent SNP G G A TCGA-AA-3956-01A-02W-0995-10 TCGA-AA-3956-10A-01W-0995-10 g.chr1:6188196G>A c.3813C>T c.(3811-3813)gaC>gaT p.D1271D COAD 1 6188585 6188585 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr1:6188585T>G c.3704A>C c.(3703-3705)aAg>aCg p.K1235T COAD 1 6188947 6188947 + Silent SNP G G A TCGA-AD-6965-01A-11D-1924-10 TCGA-AD-6965-10A-01D-1924-10 g.chr1:6188947G>A c.3570C>T c.(3568-3570)gaC>gaT p.D1190D COAD 1 6188947 6188947 + Silent SNP G G A TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr1:6188947G>A c.3570C>T c.(3568-3570)gaC>gaT p.D1190D COAD 1 6189016 6189016 + Missense_Mutation SNP C C A TCGA-A6-6141-01A-11D-1771-10 TCGA-A6-6141-10A-01D-1771-10 g.chr1:6189016C>A c.3501G>T c.(3499-3501)atG>atT p.M1167I COAD 1 6191717 6191717 + Missense_Mutation SNP C C T TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr1:6191717C>T c.3236G>A c.(3235-3237)cGg>cAg p.R1079Q COAD 1 6194862 6194863 + Frame_Shift_Ins INS - - C TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr1:6194862_6194863insC c.2927_2928insG c.(2926-2928)ggcfs p.G976fs COAD 1 6195434 6195434 + De_novo_Start_OutOfFrame SNP G G T TCGA-F4-6808-01A-11D-1835-10 TCGA-F4-6808-10A-01D-1835-10 g.chr1:6195434G>T COAD 1 6196811 6196811 + Missense_Mutation SNP G G A TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr1:6196811G>A c.2551C>T c.(2551-2553)Cgc>Tgc p.R851C COAD 1 6202223 6202223 + Missense_Mutation SNP C C T TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr1:6202223C>T c.2401G>A c.(2401-2403)Gcc>Acc p.A801T COAD 1 6202223 6202223 + Missense_Mutation SNP C C T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr1:6202223C>T c.2401G>A c.(2401-2403)Gcc>Acc p.A801T COAD 1 6202342 6202342 + Missense_Mutation SNP A A G TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr1:6202342A>G c.2282T>C c.(2281-2283)aTc>aCc p.I761T COAD 1 6202356 6202356 + Silent SNP C C T TCGA-G4-6626-01A-11D-1771-10 TCGA-G4-6626-10A-01D-1771-10 g.chr1:6202356C>T c.2268G>A c.(2266-2268)gcG>gcA p.A756A COAD 1 6202629 6202629 + Missense_Mutation SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr1:6202629C>T c.2080G>A c.(2080-2082)Gac>Aac p.D694N COAD 1 6203925 6203925 + Silent SNP C C T TCGA-AA-3655-01A-02D-1719-10 TCGA-AA-3655-11A-01D-1719-10 g.chr1:6203925C>T c.2001G>A c.(1999-2001)agG>agA p.R667R COAD 1 6203925 6203925 + Silent SNP C C T TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chr1:6203925C>T c.2001G>A c.(1999-2001)agG>agA p.R667R COAD 1 6203926 6203926 + Missense_Mutation SNP C C T TCGA-G4-6293-01A-11D-1719-10 TCGA-G4-6293-10A-01D-1719-10 g.chr1:6203926C>T c.2000G>A c.(1999-2001)aGg>aAg p.R667K COAD 1 6203927 6203927 + Missense_Mutation SNP T T C TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr1:6203927T>C c.1999A>G c.(1999-2001)Agg>Ggg p.R667G COAD 1 6203927 6203927 + Missense_Mutation SNP T T C TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chr1:6203927T>C c.1999A>G c.(1999-2001)Agg>Ggg p.R667G COAD 1 6204194 6204194 + Silent SNP C C T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr1:6204194C>T c.1824G>A c.(1822-1824)gtG>gtA p.V608V COAD 1 6209103 6209103 + De_novo_Start_OutOfFrame SNP G G A TCGA-AA-3502-01A-01D-1408-10 TCGA-AA-3502-11A-01D-1408-10 g.chr1:6209103G>A COAD 1 6209103 6209103 + De_novo_Start_OutOfFrame SNP G G A TCGA-DM-A28K-01A-21D-A16V-10 TCGA-DM-A28K-10A-01D-A16V-10 g.chr1:6209103G>A COAD 1 6209392 6209392 + Missense_Mutation SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr1:6209392C>T c.1075G>A c.(1075-1077)Gac>Aac p.D359N COAD 1 6209431 6209431 + Missense_Mutation SNP A A G TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr1:6209431A>G c.1036T>C c.(1036-1038)Tgt>Cgt p.C346R COAD 1 6211107 6211107 + Missense_Mutation SNP G G A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr1:6211107G>A c.979C>T c.(979-981)Cgc>Tgc p.R327C COAD 1 6211110 6211110 + Missense_Mutation SNP T T C TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr1:6211110T>C c.976A>G c.(976-978)Agg>Ggg p.R326G COAD 1 6212530 6212530 + Missense_Mutation SNP G G A TCGA-AA-3554-01A-01W-0833-10 TCGA-AA-3554-10A-01W-0833-10 g.chr1:6212530G>A c.812C>T c.(811-813)aCg>aTg p.T271M COAD 1 6212530 6212530 + Missense_Mutation SNP G G A TCGA-CM-4746-01A-01D-1408-10 TCGA-CM-4746-10A-01D-1408-10 g.chr1:6212530G>A c.812C>T c.(811-813)aCg>aTg p.T271M COAD 1 6228282 6228282 + Silent SNP C C T TCGA-A6-5660-01A-01D-1650-10 TCGA-A6-5660-10A-01D-1650-10 g.chr1:6228282C>T c.135G>A c.(133-135)gtG>gtA p.V45V COAD 1 6228283 6228283 + Missense_Mutation SNP A A G TCGA-CM-5868-01A-01D-1650-10 TCGA-CM-5868-10A-01D-1650-10 g.chr1:6228283A>G c.134T>C c.(133-135)gTg>gCg p.V45A COAD 1 6228305 6228305 + Missense_Mutation SNP C C A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr1:6228305C>A c.112G>T c.(112-114)Gac>Tac p.D38Y COADREAD 1 6166720 6166720 + Missense_Mutation SNP G G T TCGA-F4-6703-01A-11D-1835-10 TCGA-F4-6703-10A-01D-1835-10 g.chr1:6166720G>T c.5698C>A c.(5698-5700)Ctg>Atg p.L1900M COADREAD 1 6166758 6166758 + Frame_Shift_Del DEL G G - TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr1:6166758delG c.5660delC c.(5659-5661)ccgfs p.P1887fs COADREAD 1 6171834 6171834 + Splice_Site SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr1:6171834C>T c.e36+1 COADREAD 1 6181181 6181181 + Silent SNP C C T TCGA-AH-6549-01A-11D-1826-10 TCGA-AH-6549-10A-01D-1826-10 g.chr1:6181181C>T c.4896G>A c.(4894-4896)ccG>ccA p.P1632P COADREAD 1 6181217 6181217 + Silent SNP C C T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr1:6181217C>T c.4860G>A c.(4858-4860)gaG>gaA p.E1620E COADREAD 1 6181243 6181243 + Missense_Mutation SNP C C T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr1:6181243C>T c.4834G>A c.(4834-4836)Gcc>Acc p.A1612T COADREAD 1 6184050 6184050 + Missense_Mutation SNP C C T TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr1:6184050C>T c.4657G>A c.(4657-4659)Gcc>Acc p.A1553T COADREAD 1 6184072 6184072 + Silent SNP C C T TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chr1:6184072C>T c.4635G>A c.(4633-4635)tcG>tcA p.S1545S COADREAD 1 6184144 6184144 + Silent SNP G G A TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr1:6184144G>A c.4563C>T c.(4561-4563)aaC>aaT p.N1521N COADREAD 1 6184675 6184675 + Missense_Mutation SNP C C T TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr1:6184675C>T c.4441G>A c.(4441-4443)Gat>Aat p.D1481N COADREAD 1 6185218 6185218 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr1:6185218C>T c.4336G>A c.(4336-4338)Gcc>Acc p.A1446T COADREAD 1 6186793 6186793 + Missense_Mutation SNP C C A TCGA-G4-6307-01A-11D-1719-10 TCGA-G4-6307-10A-01D-1720-10 g.chr1:6186793C>A c.3917G>T c.(3916-3918)cGg>cTg p.R1306L COADREAD 1 6188196 6188196 + Silent SNP G G A TCGA-AA-3956-01A-02W-0995-10 TCGA-AA-3956-10A-01W-0995-10 g.chr1:6188196G>A c.3813C>T c.(3811-3813)gaC>gaT p.D1271D COADREAD 1 6188585 6188585 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr1:6188585T>G c.3704A>C c.(3703-3705)aAg>aCg p.K1235T COADREAD 1 6188947 6188947 + Silent SNP G G A TCGA-AD-6965-01A-11D-1924-10 TCGA-AD-6965-10A-01D-1924-10 g.chr1:6188947G>A c.3570C>T c.(3568-3570)gaC>gaT p.D1190D COADREAD 1 6188947 6188947 + Silent SNP G G A TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr1:6188947G>A c.3570C>T c.(3568-3570)gaC>gaT p.D1190D COADREAD 1 6189016 6189016 + Missense_Mutation SNP C C A TCGA-A6-6141-01A-11D-1771-10 TCGA-A6-6141-10A-01D-1771-10 g.chr1:6189016C>A c.3501G>T c.(3499-3501)atG>atT p.M1167I COADREAD 1 6191703 6191703 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr1:6191703C>T c.3250G>A c.(3250-3252)Gac>Aac p.D1084N COADREAD 1 6191717 6191717 + Missense_Mutation SNP C C T TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr1:6191717C>T c.3236G>A c.(3235-3237)cGg>cAg p.R1079Q COADREAD 1 6194862 6194863 + Frame_Shift_Ins INS - - C TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr1:6194862_6194863insC c.2927_2928insG c.(2926-2928)ggcfs p.G976fs COADREAD 1 6195434 6195434 + De_novo_Start_OutOfFrame SNP G G T TCGA-F4-6808-01A-11D-1835-10 TCGA-F4-6808-10A-01D-1835-10 g.chr1:6195434G>T COADREAD 1 6196811 6196811 + Missense_Mutation SNP G G A TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr1:6196811G>A c.2551C>T c.(2551-2553)Cgc>Tgc p.R851C COADREAD 1 6202223 6202223 + Missense_Mutation SNP C C T TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr1:6202223C>T c.2401G>A c.(2401-2403)Gcc>Acc p.A801T COADREAD 1 6202223 6202223 + Missense_Mutation SNP C C T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr1:6202223C>T c.2401G>A c.(2401-2403)Gcc>Acc p.A801T COADREAD 1 6202309 6202309 + Missense_Mutation SNP G G A TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr1:6202309G>A c.2315C>T c.(2314-2316)gCg>gTg p.A772V COADREAD 1 6202342 6202342 + Missense_Mutation SNP A A G TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr1:6202342A>G c.2282T>C c.(2281-2283)aTc>aCc p.I761T COADREAD 1 6202356 6202356 + Silent SNP C C T TCGA-G4-6626-01A-11D-1771-10 TCGA-G4-6626-10A-01D-1771-10 g.chr1:6202356C>T c.2268G>A c.(2266-2268)gcG>gcA p.A756A COADREAD 1 6202629 6202629 + Missense_Mutation SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr1:6202629C>T c.2080G>A c.(2080-2082)Gac>Aac p.D694N COADREAD 1 6203925 6203925 + Silent SNP C C T TCGA-AA-3655-01A-02D-1719-10 TCGA-AA-3655-11A-01D-1719-10 g.chr1:6203925C>T c.2001G>A c.(1999-2001)agG>agA p.R667R COADREAD 1 6203925 6203925 + Silent SNP C C T TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chr1:6203925C>T c.2001G>A c.(1999-2001)agG>agA p.R667R COADREAD 1 6203926 6203926 + Missense_Mutation SNP C C T TCGA-G4-6293-01A-11D-1719-10 TCGA-G4-6293-10A-01D-1719-10 g.chr1:6203926C>T c.2000G>A c.(1999-2001)aGg>aAg p.R667K COADREAD 1 6203927 6203927 + Missense_Mutation SNP T T C TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr1:6203927T>C c.1999A>G c.(1999-2001)Agg>Ggg p.R667G COADREAD 1 6203927 6203927 + Missense_Mutation SNP T T C TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chr1:6203927T>C c.1999A>G c.(1999-2001)Agg>Ggg p.R667G COADREAD 1 6204194 6204194 + Silent SNP C C T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr1:6204194C>T c.1824G>A c.(1822-1824)gtG>gtA p.V608V COADREAD 1 6209103 6209103 + De_novo_Start_OutOfFrame SNP G G A TCGA-AA-3502-01A-01D-1408-10 TCGA-AA-3502-11A-01D-1408-10 g.chr1:6209103G>A COADREAD 1 6209103 6209103 + De_novo_Start_OutOfFrame SNP G G A TCGA-DM-A28K-01A-21D-A16V-10 TCGA-DM-A28K-10A-01D-A16V-10 g.chr1:6209103G>A COADREAD 1 6209392 6209392 + Missense_Mutation SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr1:6209392C>T c.1075G>A c.(1075-1077)Gac>Aac p.D359N COADREAD 1 6209431 6209431 + Missense_Mutation SNP A A G TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr1:6209431A>G c.1036T>C c.(1036-1038)Tgt>Cgt p.C346R COADREAD 1 6211107 6211107 + Missense_Mutation SNP G G A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr1:6211107G>A c.979C>T c.(979-981)Cgc>Tgc p.R327C COADREAD 1 6211110 6211110 + Missense_Mutation SNP T T C TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr1:6211110T>C c.976A>G c.(976-978)Agg>Ggg p.R326G COADREAD 1 6212508 6212508 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr1:6212508G>A c.834C>T c.(832-834)ttC>ttT p.F278F COADREAD 1 6212530 6212530 + Missense_Mutation SNP G G A TCGA-AA-3554-01A-01W-0833-10 TCGA-AA-3554-10A-01W-0833-10 g.chr1:6212530G>A c.812C>T c.(811-813)aCg>aTg p.T271M COADREAD 1 6212530 6212530 + Missense_Mutation SNP G G A TCGA-CM-4746-01A-01D-1408-10 TCGA-CM-4746-10A-01D-1408-10 g.chr1:6212530G>A c.812C>T c.(811-813)aCg>aTg p.T271M COADREAD 1 6228223 6228223 + Missense_Mutation SNP C C T TCGA-AH-6644-01A-21D-1826-10 TCGA-AH-6644-10A-01D-1826-10 g.chr1:6228223C>T c.194G>A c.(193-195)cGg>cAg p.R65Q COADREAD 1 6228282 6228282 + Silent SNP C C T TCGA-A6-5660-01A-01D-1650-10 TCGA-A6-5660-10A-01D-1650-10 g.chr1:6228282C>T c.135G>A c.(133-135)gtG>gtA p.V45V COADREAD 1 6228283 6228283 + Missense_Mutation SNP A A G TCGA-CM-5868-01A-01D-1650-10 TCGA-CM-5868-10A-01D-1650-10 g.chr1:6228283A>G c.134T>C c.(133-135)gTg>gCg p.V45A COADREAD 1 6228305 6228305 + Missense_Mutation SNP C C A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr1:6228305C>A c.112G>T c.(112-114)Gac>Tac p.D38Y DLBC 1 6188596 6188596 + Silent SNP G G A TCGA-G8-6914-01A-11D-2210-10 TCGA-G8-6914-14A-01D-2210-10 g.chr1:6188596G>A c.3693C>T c.(3691-3693)gcC>gcT p.A1231A DLBC 1 6189098 6189098 + Missense_Mutation SNP T T A TCGA-FA-A6HN-01A-11D-A31X-10 TCGA-FA-A6HN-10A-01D-A31X-10 g.chr1:6189098T>A c.3419A>T c.(3418-3420)aAc>aTc p.N1140I DLBC 1 6196687 6196687 + Silent SNP G G T TCGA-GR-A4D5-01A-11D-A31X-10 TCGA-GR-A4D5-10A-01D-A31X-10 g.chr1:6196687G>T c.2586C>A c.(2584-2586)gtC>gtA p.V862V DLBC 1 6208928 6208928 + Missense_Mutation SNP A A T TCGA-GS-A9TY-01A-11D-A38X-10 TCGA-GS-A9TY-10A-01D-A38X-10 g.chr1:6208928A>T c.1369T>A c.(1369-1371)Tgc>Agc p.C457S DLBC 1 6208973 6208973 + De_novo_Start_OutOfFrame SNP A A C TCGA-GS-A9TY-01A-11D-A38X-10 TCGA-GS-A9TY-10A-01D-A38X-10 g.chr1:6208973A>C ESCA 1 6188230 6188230 + Missense_Mutation SNP G G A TCGA-R6-A8WC-01A-11D-A37C-09 TCGA-R6-A8WC-10A-01D-A37F-09 g.chr1:6188230G>A c.3779C>T c.(3778-3780)gCg>gTg p.A1260V ESCA 1 6188558 6188558 + Splice_Site SNP C C T TCGA-JY-A6FD-01A-11D-A33E-09 TCGA-JY-A6FD-10A-01D-A33H-09 g.chr1:6188558C>T c.e24+1 ESCA 1 6191703 6191703 + Missense_Mutation SNP C C T TCGA-JY-A93E-01A-11D-A37C-09 TCGA-JY-A93E-10A-01D-A37F-09 g.chr1:6191703C>T c.3250G>A c.(3250-3252)Gac>Aac p.D1084N ESCA 1 6196804 6196804 + Missense_Mutation SNP T T C TCGA-L5-A8NI-01A-11D-A37C-09 TCGA-L5-A8NI-11A-11D-A37F-09 g.chr1:6196804T>C c.2558A>G c.(2557-2559)aAg>aGg p.K853R ESCA 1 6202187 6202187 + Splice_Site SNP C C T TCGA-LN-A4MR-01A-11D-A28B-09 TCGA-LN-A4MR-10A-01D-A28E-09 g.chr1:6202187C>T c.e15+1 ESCA 1 6206332 6206332 + Missense_Mutation SNP C C T TCGA-L5-A4OP-01A-11D-A27G-09 TCGA-L5-A4OP-11A-11D-A27G-09 g.chr1:6206332C>T c.1742G>A c.(1741-1743)cGc>cAc p.R581H ESCA 1 6209422 6209422 + Missense_Mutation SNP A A G TCGA-L5-A4OX-01A-21D-A28B-09 TCGA-L5-A4OX-11A-13D-A28E-09 g.chr1:6209422A>G c.1045T>C c.(1045-1047)Tgc>Cgc p.C349R ESCA 1 6211155 6211155 + Missense_Mutation SNP C C T TCGA-L5-A8NU-01A-11D-A36J-09 TCGA-L5-A8NU-11A-11D-A36M-09 g.chr1:6211155C>T c.931G>A c.(931-933)Gtg>Atg p.V311M GBM 1 6171855 6171855 + Nonsense_Mutation SNP C C T TCGA-32-4213-01A-01D-1353-08 TCGA-32-4213-10A-01D-1353-08 g.chr1:6171855C>T c.5229G>A c.(5227-5229)tgG>tgA p.W1743* GBM 1 6172293 6172293 + Missense_Mutation SNP T T G TCGA-27-2519-01A-01D-1494-08 TCGA-27-2519-10A-01D-1494-08 g.chr1:6172293T>G c.5047A>C c.(5047-5049)Aat>Cat p.N1683H GBM 1 6181182 6181182 + Missense_Mutation SNP G G A TCGA-19-4068-01A-01D-1353-08 TCGA-19-4068-10A-01D-1353-08 g.chr1:6181182G>A c.4895C>T c.(4894-4896)cCg>cTg p.P1632L GBM 1 6184051 6184051 + Silent SNP G G C TCGA-76-4928-01B-01D-1486-08 TCGA-76-4928-10A-01D-1486-08 g.chr1:6184051G>C c.4656C>G c.(4654-4656)ccC>ccG p.P1552P GBM 1 6189033 6189033 + Missense_Mutation SNP C C A TCGA-14-0789-01A-01W-0424-08 TCGA-14-0789-10A-01W-0424-08 g.chr1:6189033C>A c.3484G>T c.(3484-3486)Gcc>Tcc p.A1162S GBM 1 6195434 6195434 + Missense_Mutation SNP G G A TCGA-16-1048-01B-01D-1353-08 TCGA-16-1048-10A-01D-1353-08 g.chr1:6195434G>A c.2726C>T c.(2725-2727)gCt>gTt p.A909V GBM 1 6206730 6206730 + Missense_Mutation SNP G G C TCGA-32-2495-01A-01D-1353-08 TCGA-32-2495-10B-01D-1353-08 g.chr1:6206730G>C c.1585C>G c.(1585-1587)Cta>Gta p.L529V GBM 1 6209438 6209438 + Silent SNP C C T TCGA-76-6657-01A-11D-1845-08 TCGA-76-6657-10A-01D-1845-08 g.chr1:6209438C>T c.1029G>A c.(1027-1029)caG>caA p.Q343Q GBMLGG 1 6171834 6171834 + Splice_Site SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:6171834C>T c.e36+1 GBMLGG 1 6171855 6171855 + Nonsense_Mutation SNP C C T TCGA-32-4213-01A-01D-1353-08 TCGA-32-4213-10A-01D-1353-08 g.chr1:6171855C>T c.5229G>A c.(5227-5229)tgG>tgA p.W1743* GBMLGG 1 6172293 6172293 + Missense_Mutation SNP T T G TCGA-27-2519-01A-01D-1494-08 TCGA-27-2519-10A-01D-1494-08 g.chr1:6172293T>G c.5047A>C c.(5047-5049)Aat>Cat p.N1683H GBMLGG 1 6173015 6173015 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:6173015C>A c.4956G>T c.(4954-4956)gaG>gaT p.E1652D GBMLGG 1 6181182 6181182 + Missense_Mutation SNP G G A TCGA-19-4068-01A-01D-1353-08 TCGA-19-4068-10A-01D-1353-08 g.chr1:6181182G>A c.4895C>T c.(4894-4896)cCg>cTg p.P1632L GBMLGG 1 6184051 6184051 + Silent SNP G G C TCGA-76-4928-01B-01D-1486-08 TCGA-76-4928-10A-01D-1486-08 g.chr1:6184051G>C c.4656C>G c.(4654-4656)ccC>ccG p.P1552P GBMLGG 1 6186737 6186737 + Missense_Mutation SNP G G A TCGA-DB-5281-01A-01D-1468-08 TCGA-DB-5281-10A-01D-1468-08 g.chr1:6186737G>A c.3973C>T c.(3973-3975)Cgg>Tgg p.R1325W GBMLGG 1 6189033 6189033 + Missense_Mutation SNP C C A TCGA-14-0789-01A-01W-0424-08 TCGA-14-0789-10A-01W-0424-08 g.chr1:6189033C>A c.3484G>T c.(3484-3486)Gcc>Tcc p.A1162S GBMLGG 1 6194808 6194808 + Silent SNP G G A TCGA-E1-A7YS-01A-11D-A34A-08 TCGA-E1-A7YS-10A-01D-A34A-08 g.chr1:6194808G>A c.2982C>T c.(2980-2982)aaC>aaT p.N994N GBMLGG 1 6195434 6195434 + Missense_Mutation SNP G G A TCGA-16-1048-01B-01D-1353-08 TCGA-16-1048-10A-01D-1353-08 g.chr1:6195434G>A c.2726C>T c.(2725-2727)gCt>gTt p.A909V GBMLGG 1 6202211 6202212 + Frame_Shift_Ins INS - - A TCGA-DB-5277-01A-01D-1468-08 TCGA-DB-5277-10A-01D-1468-08 g.chr1:6202211_6202212insA c.2412_2413insT c.(2410-2415)agtgggfs p.G805fs GBMLGG 1 6202326 6202326 + Silent SNP G G A TCGA-HT-8564-01A-11D-2395-08 TCGA-HT-8564-10A-01D-2396-08 g.chr1:6202326G>A c.2298C>T c.(2296-2298)cgC>cgT p.R766R GBMLGG 1 6206730 6206730 + Missense_Mutation SNP G G C TCGA-32-2495-01A-01D-1353-08 TCGA-32-2495-10B-01D-1353-08 g.chr1:6206730G>C c.1585C>G c.(1585-1587)Cta>Gta p.L529V GBMLGG 1 6209438 6209438 + Silent SNP C C T TCGA-76-6657-01A-11D-1845-08 TCGA-76-6657-10A-01D-1845-08 g.chr1:6209438C>T c.1029G>A c.(1027-1029)caG>caA p.Q343Q HNSC 1 6172998 6172998 + Missense_Mutation SNP C C A TCGA-CV-6960-01A-41D-2012-08 TCGA-CV-6960-10A-01D-2013-08 g.chr1:6172998C>A c.4973G>T c.(4972-4974)aGc>aTc p.S1658I HNSC 1 6173014 6173014 + Missense_Mutation SNP G G C TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr1:6173014G>C c.4957C>G c.(4957-4959)Ctg>Gtg p.L1653V HNSC 1 6188634 6188634 + Missense_Mutation SNP T T A TCGA-CV-5441-01A-01D-1512-08 TCGA-CV-5441-11A-01D-1512-08 g.chr1:6188634T>A c.3655A>T c.(3655-3657)Atc>Ttc p.I1219F HNSC 1 6190292 6190292 + Missense_Mutation SNP G G A TCGA-CV-A6JO-01B-11D-A34J-08 TCGA-CV-A6JO-10A-01D-A34M-08 g.chr1:6190292G>A c.3359C>T c.(3358-3360)tCg>tTg p.S1120L HNSC 1 6195309 6195309 + Missense_Mutation SNP C C T TCGA-HD-8224-01A-11D-2394-08 TCGA-HD-8224-10A-01D-2394-08 g.chr1:6195309C>T c.2851G>A c.(2851-2853)Gag>Aag p.E951K HNSC 1 6195444 6195444 + Nonsense_Mutation SNP C C A TCGA-CV-A461-01A-41D-A25Y-08 TCGA-CV-A461-10A-01D-A25Y-08 g.chr1:6195444C>A c.2716G>T c.(2716-2718)Gag>Tag p.E906* HNSC 1 6202630 6202632 + In_Frame_Del DEL GAT GAT - TCGA-CR-5247-01A-01D-2012-08 TCGA-CR-5247-10A-01D-2013-08 g.chr1:6202630_6202632delGAT c.2077_2079delATC c.(2077-2079)atcdel p.I693del HNSC 1 6209356 6209356 + Missense_Mutation SNP C C G TCGA-CQ-6221-01A-11D-2078-08 TCGA-CQ-6221-10A-01D-2078-08 g.chr1:6209356C>G c.1111G>C c.(1111-1113)Gac>Cac p.D371H HNSC 1 6214862 6214862 + Missense_Mutation SNP G G C TCGA-TN-A7HL-01A-11D-A34J-08 TCGA-TN-A7HL-10A-01D-A34M-08 g.chr1:6214862G>C c.603C>G c.(601-603)ttC>ttG p.F201L KIPAN 1 6171886 6171886 + Missense_Mutation SNP T T C TCGA-B0-4837-01A-01D-1373-10 TCGA-B0-4837-11A-01D-1373-10 g.chr1:6171886T>C c.5198A>G c.(5197-5199)tAc>tGc p.Y1733C KIPAN 1 6204188 6204188 + Silent SNP G G A TCGA-BQ-5878-01A-11D-1589-08 TCGA-BQ-5878-11A-01D-1589-08 g.chr1:6204188G>A c.1830C>T c.(1828-1830)taC>taT p.Y610Y KIPAN 1 6208965 6208965 + Missense_Mutation SNP G G T TCGA-CJ-6031-01A-11D-1669-08 TCGA-CJ-6031-11A-01D-1669-08 g.chr1:6208965G>T c.1332C>A c.(1330-1332)aaC>aaA p.N444K KIPAN 1 6211094 6211094 + Missense_Mutation SNP C C A TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr1:6211094C>A c.992G>T c.(991-993)aGg>aTg p.R331M KIPAN 1 6212475 6212475 + Silent SNP G G T TCGA-5P-A9KE-01A-11D-A42J-10 TCGA-5P-A9KE-10A-01D-A42M-10 g.chr1:6212475G>T c.867C>A c.(865-867)tcC>tcA p.S289S KIPAN 1 6212526 6212526 + Silent SNP G G A TCGA-CJ-6030-01A-11D-1669-08 TCGA-CJ-6030-11A-01D-1669-08 g.chr1:6212526G>A c.816C>T c.(814-816)gcC>gcT p.A272A KIPAN 1 6214783 6214783 + Missense_Mutation SNP C C T TCGA-B9-A8YI-01A-21D-A36X-10 TCGA-B9-A8YI-10A-01D-A370-10 g.chr1:6214783C>T c.682G>A c.(682-684)Gtc>Atc p.V228I KIPAN 1 6214898 6214898 + Silent SNP A A C TCGA-B2-5635-01A-01D-1534-10 TCGA-B2-5635-10A-01D-1535-10 g.chr1:6214898A>C c.567T>G c.(565-567)ggT>ggG p.G189G KIPAN 1 6228284 6228284 + Missense_Mutation SNP C C T TCGA-B0-4836-01A-01D-1373-10 TCGA-B0-4836-11A-01D-1373-10 g.chr1:6228284C>T c.133G>A c.(133-135)Gtg>Atg p.V45M KIRC 1 6171886 6171886 + Missense_Mutation SNP T T C TCGA-B0-4837-01A-01D-1373-10 TCGA-B0-4837-11A-01D-1373-10 g.chr1:6171886T>C c.5198A>G c.(5197-5199)tAc>tGc p.Y1733C KIRC 1 6208965 6208965 + Missense_Mutation SNP G G T TCGA-CJ-6031-01A-11D-1669-08 TCGA-CJ-6031-11A-01D-1669-08 g.chr1:6208965G>T c.1332C>A c.(1330-1332)aaC>aaA p.N444K KIRC 1 6211094 6211094 + Missense_Mutation SNP C C A TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr1:6211094C>A c.992G>T c.(991-993)aGg>aTg p.R331M KIRC 1 6212526 6212526 + Silent SNP G G A TCGA-CJ-6030-01A-11D-1669-08 TCGA-CJ-6030-11A-01D-1669-08 g.chr1:6212526G>A c.816C>T c.(814-816)gcC>gcT p.A272A KIRC 1 6214898 6214898 + Silent SNP A A C TCGA-B2-5635-01A-01D-1534-10 TCGA-B2-5635-10A-01D-1535-10 g.chr1:6214898A>C c.567T>G c.(565-567)ggT>ggG p.G189G KIRC 1 6228284 6228284 + Missense_Mutation SNP C C T TCGA-B0-4836-01A-01D-1373-10 TCGA-B0-4836-11A-01D-1373-10 g.chr1:6228284C>T c.133G>A c.(133-135)Gtg>Atg p.V45M KIRP 1 6204188 6204188 + Silent SNP G G A TCGA-BQ-5878-01A-11D-1589-08 TCGA-BQ-5878-11A-01D-1589-08 g.chr1:6204188G>A c.1830C>T c.(1828-1830)taC>taT p.Y610Y KIRP 1 6212475 6212475 + Silent SNP G G T TCGA-5P-A9KE-01A-11D-A42J-10 TCGA-5P-A9KE-10A-01D-A42M-10 g.chr1:6212475G>T c.867C>A c.(865-867)tcC>tcA p.S289S KIRP 1 6214783 6214783 + Missense_Mutation SNP C C T TCGA-B9-A8YI-01A-21D-A36X-10 TCGA-B9-A8YI-10A-01D-A370-10 g.chr1:6214783C>T c.682G>A c.(682-684)Gtc>Atc p.V228I LGG 1 6171834 6171834 + Splice_Site SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:6171834C>T c.e36+1 LGG 1 6173015 6173015 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:6173015C>A c.4956G>T c.(4954-4956)gaG>gaT p.E1652D LGG 1 6186737 6186737 + Missense_Mutation SNP G G A TCGA-DB-5281-01A-01D-1468-08 TCGA-DB-5281-10A-01D-1468-08 g.chr1:6186737G>A c.3973C>T c.(3973-3975)Cgg>Tgg p.R1325W LGG 1 6194808 6194808 + Silent SNP G G A TCGA-E1-A7YS-01A-11D-A34A-08 TCGA-E1-A7YS-10A-01D-A34A-08 g.chr1:6194808G>A c.2982C>T c.(2980-2982)aaC>aaT p.N994N LGG 1 6202211 6202212 + Frame_Shift_Ins INS - - A TCGA-DB-5277-01A-01D-1468-08 TCGA-DB-5277-10A-01D-1468-08 g.chr1:6202211_6202212insA c.2412_2413insT c.(2410-2415)agtgggfs p.G805fs LGG 1 6202326 6202326 + Silent SNP G G A TCGA-HT-8564-01A-11D-2395-08 TCGA-HT-8564-10A-01D-2396-08 g.chr1:6202326G>A c.2298C>T c.(2296-2298)cgC>cgT p.R766R LIHC 1 6188597 6188597 + Missense_Mutation SNP G G A TCGA-BC-A10W-01A-11D-A12Z-10 TCGA-BC-A10W-11A-11D-A12Z-10 g.chr1:6188597G>A c.3692C>T c.(3691-3693)gCc>gTc p.A1231V LIHC 1 6196807 6196807 + Missense_Mutation SNP A A T TCGA-G3-A25Z-01A-11D-A16V-10 TCGA-G3-A25Z-10A-01D-A16V-10 g.chr1:6196807A>T c.2555T>A c.(2554-2556)cTc>cAc p.L852H LIHC 1 6202186 6202186 + Splice_Site SNP A A G TCGA-4R-AA8I-01A-11D-A382-10 TCGA-4R-AA8I-10B-01D-A385-10 g.chr1:6202186A>G c.e15+1 LIHC 1 6202277 6202277 + Frame_Shift_Del DEL C C - TCGA-DD-A1EG-01A-11D-A20W-10 TCGA-DD-A1EG-10A-01D-A20W-10 g.chr1:6202277delC c.2347delG c.(2347-2349)gacfs p.D783fs LIHC 1 6206301 6206301 + Nonsense_Mutation SNP C C T TCGA-CC-A7IK-01A-12D-A33Q-10 TCGA-CC-A7IK-10A-01D-A33Q-10 g.chr1:6206301C>T c.1773G>A c.(1771-1773)tgG>tgA p.W591* LIHC 1 6209325 6209325 + Missense_Mutation SNP T T G TCGA-G3-AAV0-01A-11D-A36X-10 TCGA-G3-AAV0-10A-01D-A370-10 g.chr1:6209325T>G c.1142A>C c.(1141-1143)aAg>aCg p.K381T LIHC 1 6211179 6211179 + Missense_Mutation SNP T T A TCGA-DD-AACQ-01A-11D-A40R-10 TCGA-DD-AACQ-10A-01D-A40U-10 g.chr1:6211179T>A c.907A>T c.(907-909)Agc>Tgc p.S303C LIHC 1 6214807 6214807 + Missense_Mutation SNP C C T TCGA-GJ-A9DB-01A-11D-A36X-10 TCGA-GJ-A9DB-10A-01D-A370-10 g.chr1:6214807C>T c.658G>A c.(658-660)Gtc>Atc p.V220I LIHC 1 6228214 6228214 + Missense_Mutation SNP T T A TCGA-DD-AADF-01A-11D-A40R-10 TCGA-DD-AADF-10A-01D-A40U-10 g.chr1:6228214T>A c.203A>T c.(202-204)aAa>aTa p.K68I LUAD 1 6166831 6166831 + Missense_Mutation SNP G G T TCGA-L9-A444-01A-21D-A24D-08 TCGA-L9-A444-10A-01D-A24F-08 g.chr1:6166831G>T c.5587C>A c.(5587-5589)Cag>Aag p.Q1863K LUAD 1 6169915 6169915 + Missense_Mutation SNP G G T TCGA-91-6831-01A-11D-1855-08 TCGA-91-6831-11A-02D-1855-08 g.chr1:6169915G>T c.5518C>A c.(5518-5520)Cag>Aag p.Q1840K LUAD 1 6169915 6169915 + Missense_Mutation SNP G G T TCGA-MP-A4TC-01A-11D-A24P-08 TCGA-MP-A4TC-10A-01D-A24P-08 g.chr1:6169915G>T c.5518C>A c.(5518-5520)Cag>Aag p.Q1840K LUAD 1 6169998 6169998 + Missense_Mutation SNP A A T TCGA-53-7624-01A-11D-2063-08 TCGA-53-7624-10A-01D-2063-08 g.chr1:6169998A>T c.5435T>A c.(5434-5436)cTg>cAg p.L1812Q LUAD 1 6171840 6171840 + Silent SNP G G A TCGA-78-7156-01A-11D-2036-08 TCGA-78-7156-10A-01D-2036-08 g.chr1:6171840G>A c.5244C>T c.(5242-5244)atC>atT p.I1748I LUAD 1 6173020 6173020 + Silent SNP G G A TCGA-44-2656-01A-02D-0969-08 TCGA-44-2656-10A-01D-0969-08 g.chr1:6173020G>A c.4951C>T c.(4951-4953)Ctg>Ttg p.L1651L LUAD 1 6173025 6173025 + Missense_Mutation SNP T T C TCGA-69-7973-01A-11D-2184-08 TCGA-69-7973-10A-01D-2184-08 g.chr1:6173025T>C c.4946A>G c.(4945-4947)gAc>gGc p.D1649G LUAD 1 6181567 6181567 + Missense_Mutation SNP G G T TCGA-78-7155-01A-11D-2036-08 TCGA-78-7155-10A-01D-2036-08 g.chr1:6181567G>T c.4766C>A c.(4765-4767)cCc>cAc p.P1589H LUAD 1 6184629 6184629 + Missense_Mutation SNP G G C TCGA-38-4631-01A-01D-1753-08 TCGA-38-4631-11A-01D-1753-08 g.chr1:6184629G>C c.4487C>G c.(4486-4488)tCc>tGc p.S1496C LUAD 1 6185633 6185633 + Missense_Mutation SNP C C G TCGA-NJ-A4YP-01A-11D-A25L-08 TCGA-NJ-A4YP-10A-01D-A25L-08 g.chr1:6185633C>G c.4211G>C c.(4210-4212)aGg>aCg p.R1404T LUAD 1 6185835 6185835 + Nonsense_Mutation SNP C C A TCGA-44-3918-01A-01D-1105-08 TCGA-44-3918-11A-01D-1105-08 g.chr1:6185835C>A c.4162G>T c.(4162-4164)Gaa>Taa p.E1388* LUAD 1 6185838 6185838 + Missense_Mutation SNP G G T TCGA-17-Z011-01A-01W-0746-08 TCGA-17-Z011-11A-01W-0746-08 g.chr1:6185838G>T c.4159C>A c.(4159-4161)Ccg>Acg p.P1387T LUAD 1 6186638 6186638 + Missense_Mutation SNP C C A TCGA-95-7947-01A-11D-2184-08 TCGA-95-7947-10A-01D-2184-08 g.chr1:6186638C>A c.4072G>T c.(4072-4074)Gac>Tac p.D1358Y LUAD 1 6186807 6186807 + Splice_Site SNP C C T TCGA-64-1681-01A-11D-2063-08 TCGA-64-1681-10A-01D-2063-08 g.chr1:6186807C>T c.e26-1 LUAD 1 6188662 6188662 + Missense_Mutation SNP C C T TCGA-55-8301-01A-11D-2284-08 TCGA-55-8301-10A-01D-2284-08 g.chr1:6188662C>T c.3627G>A c.(3625-3627)atG>atA p.M1209I LUAD 1 6188908 6188908 + Silent SNP G G A TCGA-67-6217-01A-11D-1753-08 TCGA-67-6217-10A-01D-1753-08 g.chr1:6188908G>A c.3609C>T c.(3607-3609)gaC>gaT p.D1203D LUAD 1 6189113 6189113 + Missense_Mutation SNP T T G TCGA-55-8299-01A-11D-2284-08 TCGA-55-8299-10B-01D-2323-08 g.chr1:6189113T>G c.3404A>C c.(3403-3405)cAc>cCc p.H1135P LUAD 1 6190297 6190297 + De_novo_Start_OutOfFrame SNP G G A TCGA-78-8640-01A-11D-2393-08 TCGA-78-8640-11A-01D-2393-08 g.chr1:6190297G>A LUAD 1 6194240 6194240 + Missense_Mutation SNP T T A TCGA-05-5423-01A-01D-1625-08 TCGA-05-5423-10A-01D-1625-08 g.chr1:6194240T>A c.3092A>T c.(3091-3093)aAg>aTg p.K1031M LUAD 1 6194275 6194275 + Silent SNP C C A TCGA-05-5425-01A-02D-1625-08 TCGA-05-5425-10A-01D-1625-08 g.chr1:6194275C>A c.3057G>T c.(3055-3057)ctG>ctT p.L1019L LUAD 1 6194814 6194814 + Nonsense_Mutation SNP G G T TCGA-75-6211-01A-11D-1753-08 TCGA-75-6211-10A-01D-1753-08 g.chr1:6194814G>T c.2976C>A c.(2974-2976)tgC>tgA p.C992* LUAD 1 6194862 6194862 + Silent SNP G G T TCGA-95-A4VP-01A-21D-A25L-08 TCGA-95-A4VP-10A-01D-A25L-08 g.chr1:6194862G>T c.2928C>A c.(2926-2928)ggC>ggA p.G976G LUAD 1 6196583 6196583 + Missense_Mutation SNP C C A TCGA-99-8025-01A-11D-2238-08 TCGA-99-8025-10A-01D-2238-08 g.chr1:6196583C>A c.2690G>T c.(2689-2691)aGg>aTg p.R897M LUAD 1 6196606 6196606 + Silent SNP G G T TCGA-17-Z000-01A-01W-0746-08 TCGA-17-Z000-11A-01W-0746-08 g.chr1:6196606G>T c.2667C>A c.(2665-2667)ctC>ctA p.L889L LUAD 1 6196657 6196657 + Silent SNP C C G TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr1:6196657C>G c.2616G>C c.(2614-2616)ctG>ctC p.L872L LUAD 1 6196845 6196845 + Silent SNP G G A TCGA-62-A46O-01A-11D-A24D-08 TCGA-62-A46O-10A-01D-A24F-08 g.chr1:6196845G>A c.2517C>T c.(2515-2517)atC>atT p.I839I LUAD 1 6196890 6196890 + Silent SNP G G T TCGA-55-A48X-01A-11D-A24D-08 TCGA-55-A48X-10A-01D-A24F-08 g.chr1:6196890G>T c.2472C>A c.(2470-2472)acC>acA p.T824T LUAD 1 6202265 6202265 + Missense_Mutation SNP G G A TCGA-17-Z050-01A-01W-0747-08 TCGA-17-Z050-11A-01W-0747-08 g.chr1:6202265G>A c.2359C>T c.(2359-2361)Cgc>Tgc p.R787C LUAD 1 6202513 6202513 + Silent SNP C C A TCGA-17-Z022-01A-01W-0746-08 TCGA-17-Z022-11A-01W-0746-08 g.chr1:6202513C>A c.2196G>T c.(2194-2196)acG>acT p.T732T LUAD 1 6203888 6203888 + Missense_Mutation SNP C C A TCGA-50-5939-01A-11D-1625-08 TCGA-50-5939-11A-01D-1625-08 g.chr1:6203888C>A c.2038G>T c.(2038-2040)Gtg>Ttg p.V680L LUAD 1 6203951 6203951 + Missense_Mutation SNP G G C TCGA-78-8640-01A-11D-2393-08 TCGA-78-8640-11A-01D-2393-08 g.chr1:6203951G>C c.1975C>G c.(1975-1977)Ctg>Gtg p.L659V LUAD 1 6203990 6203990 + Splice_Site SNP C C A TCGA-MP-A4T4-01A-11D-A25L-08 TCGA-MP-A4T4-10A-01D-A25L-08 g.chr1:6203990C>A c.1936G>T c.(1936-1938)Gag>Tag p.E646* LUAD 1 6203992 6203992 + Splice_Site SNP C C A TCGA-50-5045-01A-01D-1625-08 TCGA-50-5045-10A-01D-1625-08 g.chr1:6203992C>A c.e13-1 LUAD 1 6204158 6204158 + Silent SNP G G A TCGA-55-8620-01A-11D-2393-08 TCGA-55-8620-10A-01D-2393-08 g.chr1:6204158G>A c.1860C>T c.(1858-1860)gaC>gaT p.D620D LUAD 1 6206324 6206324 + Missense_Mutation SNP G G A TCGA-55-7727-01A-11D-2167-08 TCGA-55-7727-10A-01D-2167-08 g.chr1:6206324G>A c.1750C>T c.(1750-1752)Cgc>Tgc p.R584C LUAD 1 6206332 6206332 + Missense_Mutation SNP C C A TCGA-50-6590-01A-12D-1855-08 TCGA-50-6590-11A-01D-1855-08 g.chr1:6206332C>A c.1742G>T c.(1741-1743)cGc>cTc p.R581L LUAD 1 6206398 6206398 + Missense_Mutation SNP C C T TCGA-78-7155-01A-11D-2036-08 TCGA-78-7155-10A-01D-2036-08 g.chr1:6206398C>T c.1676G>A c.(1675-1677)gGg>gAg p.G559E LUAD 1 6206411 6206411 + Missense_Mutation SNP C C G TCGA-MP-A4TK-01A-11D-A24P-08 TCGA-MP-A4TK-10A-01D-A24P-08 g.chr1:6206411C>G c.1663G>C c.(1663-1665)Gac>Cac p.D555H LUAD 1 6206463 6206463 + Silent SNP C C A TCGA-38-4625-01A-01D-1553-08 TCGA-38-4625-11A-01D-1553-08 g.chr1:6206463C>A c.1611G>T c.(1609-1611)gtG>gtT p.V537V LUAD 1 6208915 6208915 + Splice_Site SNP G G T TCGA-NJ-A4YF-01A-12D-A25L-08 TCGA-NJ-A4YF-10A-01D-A25L-08 g.chr1:6208915G>T c.1382C>A c.(1381-1383)aCt>aAt p.T461N LUAD 1 6208916 6208916 + Missense_Mutation SNP T T C TCGA-L9-A443-01A-12D-A24D-08 TCGA-L9-A443-10A-01D-A24F-08 g.chr1:6208916T>C c.1381A>G c.(1381-1383)Act>Gct p.T461A LUAD 1 6208940 6208940 + Missense_Mutation SNP C C T TCGA-78-8662-01A-11D-2393-08 TCGA-78-8662-10A-01D-2393-08 g.chr1:6208940C>T c.1357G>A c.(1357-1359)Ggt>Agt p.G453S LUAD 1 6209425 6209425 + Missense_Mutation SNP C C A TCGA-86-8073-01A-11D-2238-08 TCGA-86-8073-10A-01D-2238-08 g.chr1:6209425C>A c.1042G>T c.(1042-1044)Gtg>Ttg p.V348L LUAD 1 6211173 6211173 + Missense_Mutation SNP T T A TCGA-69-7765-01A-11D-2167-08 TCGA-69-7765-10A-01D-2167-08 g.chr1:6211173T>A c.913A>T c.(913-915)Agc>Tgc p.S305C LUAD 1 6212594 6212594 + Missense_Mutation SNP G G T TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr1:6212594G>T c.748C>A c.(748-750)Cct>Act p.P250T LUAD 1 6214763 6214763 + Silent SNP G G A TCGA-95-7043-01A-11D-1945-08 TCGA-95-7043-10A-01D-1946-08 g.chr1:6214763G>A c.702C>T c.(700-702)ccC>ccT p.P234P LUAD 1 6214773 6214773 + Missense_Mutation SNP G G A TCGA-05-4390-01A-02D-1753-08 TCGA-05-4390-10A-01D-1753-08 g.chr1:6214773G>A c.692C>T c.(691-693)cCg>cTg p.P231L LUAD 1 6214849 6214849 + Missense_Mutation SNP C C A TCGA-50-5930-01A-11D-1753-08 TCGA-50-5930-11A-01D-1753-08 g.chr1:6214849C>A c.616G>T c.(616-618)Gcg>Tcg p.A206S LUSC 1 6169927 6169927 + Missense_Mutation SNP C C T TCGA-43-3394-01A-01D-0983-08 TCGA-43-3394-10A-01D-0983-08 g.chr1:6169927C>T c.5506G>A c.(5506-5508)Gcc>Acc p.A1836T LUSC 1 6169932 6169932 + Missense_Mutation SNP C C T TCGA-22-1016-01A-01D-1521-08 TCGA-22-1016-11A-01D-1521-08 g.chr1:6169932C>T c.5501G>A c.(5500-5502)tGc>tAc p.C1834Y LUSC 1 6170001 6170001 + Missense_Mutation SNP T T C TCGA-46-3769-01A-01D-0983-08 TCGA-46-3769-10A-01D-0983-08 g.chr1:6170001T>C c.5432A>G c.(5431-5433)tAc>tGc p.Y1811C LUSC 1 6185836 6185836 + Silent SNP C C T TCGA-21-1071-01A-01D-1521-08 TCGA-21-1071-11A-01D-1521-08 g.chr1:6185836C>T c.4161G>A c.(4159-4161)ccG>ccA p.P1387P LUSC 1 6194301 6194301 + Missense_Mutation SNP T T C TCGA-56-6546-01A-11D-1817-08 TCGA-56-6546-10A-01D-1817-08 g.chr1:6194301T>C c.3031A>G c.(3031-3033)Aat>Gat p.N1011D LUSC 1 6196587 6196587 + Nonsense_Mutation SNP C C A TCGA-22-5472-01A-01D-1632-08 TCGA-22-5472-11A-11D-1632-08 g.chr1:6196587C>A c.2686G>T c.(2686-2688)Gag>Tag p.E896* LUSC 1 6196612 6196612 + Silent SNP G G A TCGA-60-2720-01A-01D-1522-08 TCGA-60-2720-11A-01D-1522-08 g.chr1:6196612G>A c.2661C>T c.(2659-2661)ttC>ttT p.F887F LUSC 1 6202587 6202587 + Missense_Mutation SNP G G A TCGA-33-6737-01A-11D-1817-08 TCGA-33-6737-11A-01D-1817-08 g.chr1:6202587G>A c.2122C>T c.(2122-2124)Ctc>Ttc p.L708F LUSC 1 6202664 6202664 + Splice_Site SNP G G A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr1:6202664G>A c.2045C>T c.(2044-2046)cCc>cTc p.P682L LUSC 1 6206373 6206373 + Missense_Mutation SNP C C A TCGA-18-3416-01A-01D-0983-08 TCGA-18-3416-11A-01D-0983-08 g.chr1:6206373C>A c.1701G>T c.(1699-1701)aaG>aaT p.K567N LUSC 1 6206386 6206386 + Frame_Shift_Del DEL C C - TCGA-66-2756-01A-01D-1522-08 TCGA-66-2756-11A-01D-1522-08 g.chr1:6206386delC c.1688delG c.(1687-1689)ggcfs p.G563fs LUSC 1 6212538 6212538 + Silent SNP C C T TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr1:6212538C>T c.804G>A c.(802-804)ggG>ggA p.G268G OV 1 6170036 6170036 + Silent SNP C C T TCGA-36-2530-01A-01D-1526-09 TCGA-36-2530-10A-01D-1526-09 g.chr1:6170036C>T c.5397G>A c.(5395-5397)gcG>gcA p.A1799A OV 1 6189018 6189018 + Missense_Mutation SNP T T C TCGA-09-2049-01D-01W-0799-08 TCGA-09-2049-10A-01W-0799-08 g.chr1:6189018T>C c.3499A>G c.(3499-3501)Atg>Gtg p.M1167V OV 1 6191693 6191693 + Missense_Mutation SNP T T A TCGA-36-2552-01A-01D-1526-09 TCGA-36-2552-10A-01D-1526-09 g.chr1:6191693T>A c.3260A>T c.(3259-3261)aAt>aTt p.N1087I OV 1 6202548 6202548 + Missense_Mutation SNP T T A TCGA-13-2059-01A-01D-1526-09 TCGA-13-2059-10A-01D-1526-09 g.chr1:6202548T>A c.2161A>T c.(2161-2163)Acc>Tcc p.T721S OV 1 6206923 6206924 + Frame_Shift_Ins INS - - G TCGA-24-1464-01A-01W-0549-09 TCGA-24-1464-10A-01W-0549-09 g.chr1:6206923_6206924insG c.1391_1392insC c.(1390-1392)ccafs p.P464fs PAAD 1 6166503 6166503 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr1:6166503C>T c.5809G>A c.(5809-5811)Gga>Aga p.G1937R PAAD 1 6169927 6169927 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr1:6169927C>T c.5506G>A c.(5506-5508)Gcc>Acc p.A1836T PAAD 1 6181169 6181169 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr1:6181169C>T c.4908G>A c.(4906-4908)ccG>ccA p.P1636P PAAD 1 6184720 6184720 + Splice_Site SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr1:6184720C>A c.4396G>T c.(4396-4398)Gcc>Tcc p.A1466S PAAD 1 6190296 6190296 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr1:6190296C>T c.3355G>A c.(3355-3357)Gac>Aac p.D1119N PAAD 1 6202222 6202222 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr1:6202222G>A c.2402C>T c.(2401-2403)gCc>gTc p.A801V PAAD 1 6202537 6202537 + Silent SNP G G A TCGA-RL-AAAS-01A-32D-A397-08 TCGA-RL-AAAS-10A-01D-A39A-08 g.chr1:6202537G>A c.2172C>T c.(2170-2172)gcC>gcT p.A724A PAAD 1 6211106 6211106 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr1:6211106C>T c.980G>A c.(979-981)cGc>cAc p.R327H PAAD 1 6214959 6214959 + Splice_Site SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr1:6214959C>T c.e5-1 PAAD 1 6215750 6215750 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr1:6215750C>A c.415G>T c.(415-417)Gcc>Tcc p.A139S PCPG 1 6202616 6202616 + Missense_Mutation SNP C C T TCGA-W2-A7H7-01A-11D-A35I-08 TCGA-W2-A7H7-10A-01D-A35G-08 g.chr1:6202616C>T c.2093G>A c.(2092-2094)gGc>gAc p.G698D PRAD 1 6166702 6166702 + Missense_Mutation SNP G G A TCGA-HC-7211-01A-11D-2114-08 TCGA-HC-7211-11A-01D-2114-08 g.chr1:6166702G>A c.5716C>T c.(5716-5718)Cgc>Tgc p.R1906C PRAD 1 6166714 6166714 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr1:6166714G>A c.5704C>T c.(5704-5706)Cgc>Tgc p.R1902C PRAD 1 6181216 6181216 + Missense_Mutation SNP G G A TCGA-KK-A59V-01A-11D-A29Q-08 TCGA-KK-A59V-11A-11D-A29Q-08 g.chr1:6181216G>A c.4861C>T c.(4861-4863)Cgg>Tgg p.R1621W PRAD 1 6194781 6194781 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr1:6194781G>A c.3009C>T c.(3007-3009)gcC>gcT p.A1003A PRAD 1 6202222 6202222 + Missense_Mutation SNP G G A TCGA-G9-7509-01A-11D-A41K-08 TCGA-G9-7509-10A-01D-A41N-08 g.chr1:6202222G>A c.2402C>T c.(2401-2403)gCc>gTc p.A801V PRAD 1 6202613 6202613 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr1:6202613G>A c.2096C>T c.(2095-2097)aCa>aTa p.T699I PRAD 1 6206323 6206323 + Missense_Mutation SNP C C T TCGA-YL-A8S8-01A-11D-A377-08 TCGA-YL-A8S8-10A-01D-A37A-08 g.chr1:6206323C>T c.1751G>A c.(1750-1752)cGc>cAc p.R584H PRAD 1 6228311 6228311 + Missense_Mutation SNP A A T TCGA-HC-8216-01A-11D-A29Q-08 TCGA-HC-8216-10A-01D-A29Q-08 g.chr1:6228311A>T c.106T>A c.(106-108)Ttc>Atc p.F36I READ 1 6181181 6181181 + Silent SNP C C T TCGA-AH-6549-01A-11D-1826-10 TCGA-AH-6549-10A-01D-1826-10 g.chr1:6181181C>T c.4896G>A c.(4894-4896)ccG>ccA p.P1632P READ 1 6184050 6184050 + Missense_Mutation SNP C C T TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr1:6184050C>T c.4657G>A c.(4657-4659)Gcc>Acc p.A1553T READ 1 6191703 6191703 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr1:6191703C>T c.3250G>A c.(3250-3252)Gac>Aac p.D1084N READ 1 6202309 6202309 + Missense_Mutation SNP G G A TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr1:6202309G>A c.2315C>T c.(2314-2316)gCg>gTg p.A772V READ 1 6212508 6212508 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr1:6212508G>A c.834C>T c.(832-834)ttC>ttT p.F278F READ 1 6228223 6228223 + Missense_Mutation SNP C C T TCGA-AH-6644-01A-21D-1826-10 TCGA-AH-6644-10A-01D-1826-10 g.chr1:6228223C>T c.194G>A c.(193-195)cGg>cAg p.R65Q SARC 1 6195407 6195407 + Missense_Mutation SNP T T A TCGA-X6-A7W8-01A-21D-A351-09 TCGA-X6-A7W8-10A-01D-A351-09 g.chr1:6195407T>A c.2753A>T c.(2752-2754)aAg>aTg p.K918M SARC 1 6204083 6204083 + Splice_Site SNP C C T TCGA-DX-A8BP-01A-11D-A37C-09 TCGA-DX-A8BP-10A-01D-A37F-09 g.chr1:6204083C>T c.e12+1 SARC 1 6204084 6204084 + Splice_Site SNP C C T TCGA-DX-A8BP-01A-11D-A37C-09 TCGA-DX-A8BP-10A-01D-A37F-09 g.chr1:6204084C>T c.1934G>A c.(1933-1935)aGg>aAg p.R645K SARC 1 6206323 6206323 + Missense_Mutation SNP C C T TCGA-VT-A80J-01A-11D-A36J-09 TCGA-VT-A80J-11A-22D-A36M-09 g.chr1:6206323C>T c.1751G>A c.(1750-1752)cGc>cAc p.R584H SARC 1 6209365 6209365 + Missense_Mutation SNP C C T TCGA-DX-A48N-01A-11D-A307-09 TCGA-DX-A48N-10A-01D-A307-09 g.chr1:6209365C>T c.1102G>A c.(1102-1104)Gta>Ata p.V368I SARC 1 6214848 6214848 + Missense_Mutation SNP G G A TCGA-DX-A7EU-01A-22D-A36J-09 TCGA-DX-A7EU-10A-01D-A36M-09 g.chr1:6214848G>A c.617C>T c.(616-618)gCg>gTg p.A206V SKCM 1 6166483 6166483 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr1:6166483G>A c.5829C>T c.(5827-5829)aaC>aaT p.N1943N SKCM 1 6166762 6166762 + Missense_Mutation SNP G G A TCGA-D9-A3Z1-06A-11D-A23B-08 TCGA-D9-A3Z1-10A-01D-A23B-08 g.chr1:6166762G>A c.5656C>T c.(5656-5658)Ccc>Tcc p.P1886S SKCM 1 6169886 6169886 + Silent SNP C C T TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr1:6169886C>T c.5547G>A c.(5545-5547)ggG>ggA p.G1849G SKCM 1 6171884 6171884 + Missense_Mutation SNP C C T TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr1:6171884C>T c.5200G>A c.(5200-5202)Gac>Aac p.D1734N SKCM 1 6172243 6172243 + Silent SNP C C T TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr1:6172243C>T c.5097G>A c.(5095-5097)ggG>ggA p.G1699G SKCM 1 6173030 6173030 + Silent SNP G G A TCGA-FS-A4F5-06A-11D-A25O-08 TCGA-FS-A4F5-10B-01D-A25O-08 g.chr1:6173030G>A c.4941C>T c.(4939-4941)atC>atT p.I1647I SKCM 1 6181208 6181208 + Silent SNP C C T TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr1:6181208C>T c.4869G>A c.(4867-4869)gaG>gaA p.E1623E SKCM 1 6181214 6181214 + Silent SNP C C T TCGA-FS-A1ZC-06A-11D-A197-08 TCGA-FS-A1ZC-10A-01D-A199-08 g.chr1:6181214C>T c.4863G>A c.(4861-4863)cgG>cgA p.R1621R SKCM 1 6181563 6181563 + Silent SNP C C T TCGA-D9-A148-06A-11D-A19A-08 TCGA-D9-A148-10A-01D-A19A-08 g.chr1:6181563C>T c.4770G>A c.(4768-4770)ctG>ctA p.L1590L SKCM 1 6184071 6184071 + Missense_Mutation SNP C C T TCGA-GN-A267-06A-21D-A196-08 TCGA-GN-A267-10A-01D-A198-08 g.chr1:6184071C>T c.4636G>A c.(4636-4638)Gac>Aac p.D1546N SKCM 1 6184100 6184100 + Missense_Mutation SNP C C T TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr1:6184100C>T c.4607G>A c.(4606-4608)gGg>gAg p.G1536E SKCM 1 6184111 6184111 + Silent SNP C C T TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr1:6184111C>T c.4596G>A c.(4594-4596)gaG>gaA p.E1532E SKCM 1 6184141 6184141 + Silent SNP C C T TCGA-DA-A3F8-06A-11D-A20D-08 TCGA-DA-A3F8-10A-01D-A20D-08 g.chr1:6184141C>T c.4566G>A c.(4564-4566)ggG>ggA p.G1522G SKCM 1 6184141 6184141 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr1:6184141C>T c.4566G>A c.(4564-4566)ggG>ggA p.G1522G SKCM 1 6184610 6184610 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr1:6184610G>A c.4506C>T c.(4504-4506)acC>acT p.T1502T SKCM 1 6184666 6184666 + Missense_Mutation SNP C C T TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr1:6184666C>T c.4450G>A c.(4450-4452)Gag>Aag p.E1484K SKCM 1 6185624 6185624 + Missense_Mutation SNP G G A TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr1:6185624G>A c.4220C>T c.(4219-4221)cCc>cTc p.P1407L SKCM 1 6185911 6185911 + Silent SNP C C T TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr1:6185911C>T c.4086G>A c.(4084-4086)caG>caA p.Q1362Q SKCM 1 6188166 6188166 + Missense_Mutation SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr1:6188166C>T c.3843G>A c.(3841-3843)atG>atA p.M1281I SKCM 1 6188267 6188267 + Missense_Mutation SNP C C T TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr1:6188267C>T c.3742G>A c.(3742-3744)Gac>Aac p.D1248N SKCM 1 6188268 6188268 + Silent SNP C C T TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr1:6188268C>T c.3741G>A c.(3739-3741)aaG>aaA p.K1247K SKCM 1 6188564 6188564 + Missense_Mutation SNP G G A TCGA-EE-A2GM-06B-11D-A196-08 TCGA-EE-A2GM-10A-01D-A198-08 g.chr1:6188564G>A c.3725C>T c.(3724-3726)cCg>cTg p.P1242L SKCM 1 6188565 6188565 + Missense_Mutation SNP G G A TCGA-EE-A2GM-06B-11D-A196-08 TCGA-EE-A2GM-10A-01D-A198-08 g.chr1:6188565G>A c.3724C>T c.(3724-3726)Ccg>Tcg p.P1242S SKCM 1 6188922 6188922 + Missense_Mutation SNP C C T TCGA-FS-A1Z3-06A-11D-A197-08 TCGA-FS-A1Z3-10A-01D-A199-08 g.chr1:6188922C>T c.3595G>A c.(3595-3597)Gaa>Aaa p.E1199K SKCM 1 6188925 6188925 + Missense_Mutation SNP C C T TCGA-D3-A51R-06A-11D-A25O-08 TCGA-D3-A51R-10A-01D-A25O-08 g.chr1:6188925C>T c.3592G>A c.(3592-3594)Gag>Aag p.E1198K SKCM 1 6188969 6188969 + Missense_Mutation SNP G G A TCGA-FS-A1ZA-06A-11D-A197-08 TCGA-FS-A1ZA-10A-01D-A199-08 g.chr1:6188969G>A c.3548C>T c.(3547-3549)tCc>tTc p.S1183F SKCM 1 6189052 6189052 + Silent SNP C C T TCGA-D3-A51G-06A-11D-A25O-08 TCGA-D3-A51G-10A-01D-A25O-08 g.chr1:6189052C>T c.3465G>A c.(3463-3465)gaG>gaA p.E1155E SKCM 1 6189094 6189094 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr1:6189094C>T c.3423G>A c.(3421-3423)aaG>aaA p.K1141K SKCM 1 6191793 6191793 + Missense_Mutation SNP C C T TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr1:6191793C>T c.3160G>A c.(3160-3162)Gac>Aac p.D1054N SKCM 1 6194187 6194187 + Splice_Site SNP C C T TCGA-EE-A2MU-06A-21D-A196-08 TCGA-EE-A2MU-10A-01D-A198-08 g.chr1:6194187C>T c.e20+1 SKCM 1 6194297 6194297 + Missense_Mutation SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr1:6194297C>T c.3035G>A c.(3034-3036)gGc>gAc p.G1012D SKCM 1 6194852 6194852 + Missense_Mutation SNP C C T TCGA-EE-A3JI-06A-11D-A21A-08 TCGA-EE-A3JI-10A-01D-A21A-08 g.chr1:6194852C>T c.2938G>A c.(2938-2940)Gta>Ata p.V980I SKCM 1 6194871 6194871 + Silent SNP G G A TCGA-ER-A19Q-06A-11D-A197-08 TCGA-ER-A19Q-10A-01D-A199-08 g.chr1:6194871G>A c.2919C>T c.(2917-2919)tcC>tcT p.S973S SKCM 1 6195313 6195313 + Silent SNP C C T TCGA-GN-A26A-06A-11D-A19A-08 TCGA-GN-A26A-10A-01D-A19A-08 g.chr1:6195313C>T c.2847G>A c.(2845-2847)cgG>cgA p.R949R SKCM 1 6195421 6195421 + Silent SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr1:6195421C>T c.2739G>A c.(2737-2739)aaG>aaA p.K913K SKCM 1 6202196 6202196 + Missense_Mutation SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr1:6202196G>A c.2428C>T c.(2428-2430)Cgt>Tgt p.R810C SKCM 1 6202197 6202197 + Silent SNP G G A TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr1:6202197G>A c.2427C>T c.(2425-2427)ttC>ttT p.F809F SKCM 1 6202251 6202251 + Silent SNP C C T TCGA-EE-A29V-06A-12D-A197-08 TCGA-EE-A29V-10A-01D-A199-08 g.chr1:6202251C>T c.2373G>A c.(2371-2373)cgG>cgA p.R791R SKCM 1 6202331 6202331 + Missense_Mutation SNP C C T TCGA-EE-A2GI-06A-11D-A196-08 TCGA-EE-A2GI-10A-01D-A198-08 g.chr1:6202331C>T c.2293G>A c.(2293-2295)Gaa>Aaa p.E765K SKCM 1 6203900 6203900 + Missense_Mutation SNP C C T TCGA-EE-A2GP-06A-11D-A197-08 TCGA-EE-A2GP-10A-01D-A199-08 g.chr1:6203900C>T c.2026G>A c.(2026-2028)Gac>Aac p.D676N SKCM 1 6203924 6203924 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr1:6203924C>T c.2002G>A c.(2002-2004)Gac>Aac p.D668N SKCM 1 6203991 6203991 + Splice_Site SNP C C T TCGA-EE-A29V-06A-12D-A197-08 TCGA-EE-A29V-10A-01D-A199-08 g.chr1:6203991C>T c.1935G>A c.(1933-1935)agG>agA p.R645R SKCM 1 6204140 6204140 + Silent SNP G G A TCGA-D3-A5GN-06A-11D-A27K-08 TCGA-D3-A5GN-10A-01D-A27N-08 g.chr1:6204140G>A c.1878C>T c.(1876-1878)atC>atT p.I626I SKCM 1 6204140 6204140 + Silent SNP G G A TCGA-FS-A4F0-06A-11D-A24R-08 TCGA-FS-A4F0-10A-01D-A24R-08 g.chr1:6204140G>A c.1878C>T c.(1876-1878)atC>atT p.I626I SKCM 1 6204140 6204140 + Silent SNP G G A TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr1:6204140G>A c.1878C>T c.(1876-1878)atC>atT p.I626I SKCM 1 6204202 6204202 + Missense_Mutation SNP C C T TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr1:6204202C>T c.1816G>A c.(1816-1818)Ggg>Agg p.G606R SKCM 1 6206302 6206302 + Nonsense_Mutation SNP C C T TCGA-EE-A2MG-06A-11D-A197-08 TCGA-EE-A2MG-10A-01D-A199-08 g.chr1:6206302C>T c.1772G>A c.(1771-1773)tGg>tAg p.W591* SKCM 1 6206310 6206310 + Silent SNP C C T TCGA-EE-A2A0-06A-11D-A196-08 TCGA-EE-A2A0-10A-01D-A198-08 g.chr1:6206310C>T c.1764G>A c.(1762-1764)aaG>aaA p.K588K SKCM 1 6206355 6206355 + Silent SNP G G A TCGA-EE-A2ML-06A-11D-A197-08 TCGA-EE-A2ML-10A-01D-A199-08 g.chr1:6206355G>A c.1719C>T c.(1717-1719)ccC>ccT p.P573P SKCM 1 6206387 6206387 + Missense_Mutation SNP C C T TCGA-QB-A6FS-06A-11D-A30X-08 TCGA-QB-A6FS-10A-01D-A30X-08 g.chr1:6206387C>T c.1687G>A c.(1687-1689)Ggc>Agc p.G563S SKCM 1 6206398 6206398 + Missense_Mutation SNP C C T TCGA-D3-A2J8-06A-11D-A196-08 TCGA-D3-A2J8-10A-01D-A198-08 g.chr1:6206398C>T c.1676G>A c.(1675-1677)gGg>gAg p.G559E SKCM 1 6206416 6206416 + Missense_Mutation SNP G G A TCGA-D9-A1JW-06A-11D-A19A-08 TCGA-D9-A1JW-10A-01D-A19A-08 g.chr1:6206416G>A c.1658C>T c.(1657-1659)cCc>cTc p.P553L SKCM 1 6206417 6206417 + Missense_Mutation SNP G G A TCGA-D9-A1JW-06A-11D-A19A-08 TCGA-D9-A1JW-10A-01D-A19A-08 g.chr1:6206417G>A c.1657C>T c.(1657-1659)Ccc>Tcc p.P553S SKCM 1 6206765 6206765 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr1:6206765C>T c.1550G>A c.(1549-1551)gGg>gAg p.G517E SKCM 1 6209357 6209357 + Silent SNP C C T TCGA-EE-A17X-06A-11D-A197-08 TCGA-EE-A17X-10A-01D-A199-08 g.chr1:6209357C>T c.1110G>A c.(1108-1110)ctG>ctA p.L370L SKCM 1 6209413 6209413 + Missense_Mutation SNP C C T TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr1:6209413C>T c.1054G>A c.(1054-1056)Ggt>Agt p.G352S SKCM 1 6212510 6212510 + Missense_Mutation SNP A A T TCGA-EB-A5UL-06A-11D-A30X-08 TCGA-EB-A5UL-10A-01D-A30X-08 g.chr1:6212510A>T c.832T>A c.(832-834)Ttc>Atc p.F278I SKCM 1 6214775 6214775 + Silent SNP G G A TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr1:6214775G>A c.690C>T c.(688-690)ccC>ccT p.P230P SKCM 1 6214776 6214776 + Missense_Mutation SNP G G A TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr1:6214776G>A c.689C>T c.(688-690)cCc>cTc p.P230L SKCM 1 6214781 6214781 + Silent SNP G G A TCGA-FS-A1ZA-06A-11D-A197-08 TCGA-FS-A1ZA-10A-01D-A199-08 g.chr1:6214781G>A c.684C>T c.(682-684)gtC>gtT p.V228V SKCM 1 6214928 6214928 + Silent SNP G G A TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr1:6214928G>A c.537C>T c.(535-537)atC>atT p.I179I SKCM 1 6214931 6214931 + Silent SNP C C T TCGA-EB-A5UN-06A-11D-A30X-08 TCGA-EB-A5UN-10A-01D-A30X-08 g.chr1:6214931C>T c.534G>A c.(532-534)aaG>aaA p.K178K SKCM 1 6215778 6215778 + Splice_Site SNP C C T TCGA-DA-A1I0-06A-11D-A20D-08 TCGA-DA-A1I0-10B-01D-A20D-08 g.chr1:6215778C>T c.e4-1 SKCM 1 6219501 6219501 + Silent SNP G G A TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr1:6219501G>A c.282C>T c.(280-282)tcC>tcT p.S94S SKCM 1 6219548 6219548 + Missense_Mutation SNP C C T TCGA-D3-A2JF-06A-11D-A196-08 TCGA-D3-A2JF-10A-01D-A198-08 g.chr1:6219548C>T c.235G>A c.(235-237)Gaa>Aaa p.E79K SKCM 1 6228297 6228297 + Silent SNP G G A TCGA-D9-A3Z1-06A-11D-A23B-08 TCGA-D9-A3Z1-10A-01D-A23B-08 g.chr1:6228297G>A c.120C>T c.(118-120)ttC>ttT p.F40F SKCM 1 6228297 6228297 + Silent SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr1:6228297G>A c.120C>T c.(118-120)ttC>ttT p.F40F SKCM 1 6228297 6228297 + Silent SNP G G A TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr1:6228297G>A c.120C>T c.(118-120)ttC>ttT p.F40F SKCM 1 6228308 6228308 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr1:6228308C>T c.109G>A c.(109-111)Gat>Aat p.D37N SKCM 1 6228309 6228309 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr1:6228309G>A c.108C>T c.(106-108)ttC>ttT p.F36F SKCM 1 6228338 6228338 + Splice_Site SNP C C T TCGA-D3-A3MR-06A-11D-A21A-08 TCGA-D3-A3MR-10A-01D-A21A-08 g.chr1:6228338C>T c.e2-1

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 6170581 6170581 single base substitution C A 3_prime_UTR_variant BLCA-CN 1 6170581 6170581 single base substitution C A missense_variant G1752V 5255G>T BLCA-CN 1 6170581 6170581 single base substitution C A missense_variant G609V 1826G>T BLCA-CN 1 6170581 6170581 single base substitution C A upstream_gene_variant BLCA-CN 1 6170582 6170582 single base substitution C A 3_prime_UTR_variant BLCA-CN 1 6170582 6170582 single base substitution C A missense_variant G1752C 5254G>T BLCA-CN 1 6170582 6170582 single base substitution C A missense_variant G609C 1825G>T BLCA-CN 1 6170582 6170582 single base substitution C A upstream_gene_variant BLCA-CN 1 6171937 6171937 single base substitution T C 3_prime_UTR_variant BLCA-CN 1 6171937 6171937 single base substitution T C missense_variant H1716R 5147A>G BLCA-CN 1 6171937 6171937 single base substitution T C missense_variant H573R 1718A>G BLCA-CN 1 6188977 6188977 single base substitution C A 3_prime_UTR_variant BLCA-CN 1 6188977 6188977 single base substitution C A exon_variant BLCA-CN 1 6188977 6188977 single base substitution C A intron_variant BLCA-CN 1 6188977 6188977 single base substitution C A missense_variant K1180N 3540G>T BLCA-CN 1 6188977 6188977 single base substitution C A missense_variant K37N 111G>T BLCA-CN 1 6188977 6188977 single base substitution C A upstream_gene_variant BLCA-CN 1 6190315 6190315 single base substitution C T 5_prime_UTR_variant BLCA-CN 1 6190315 6190315 single base substitution C T exon_variant BLCA-CN 1 6190315 6190315 single base substitution C T synonymous_variant A1112A 3336G>A BLCA-CN 1 6190315 6190315 single base substitution C T upstream_gene_variant BLCA-CN 1 6202350 6202350 single base substitution G A 5_prime_UTR_variant BLCA-CN 1 6202350 6202350 single base substitution G A exon_variant BLCA-CN 1 6202350 6202350 single base substitution G A synonymous_variant L758L 2274C>T BLCA-CN 1 6202568 6202568 single base substitution G C 5_prime_UTR_premature_start_codon_gain_variant BLCA-CN 1 6202568 6202568 single base substitution G C exon_variant BLCA-CN 1 6202568 6202568 single base substitution G C missense_variant S714C 2141C>G BLCA-CN 1 6215673 6215673 single base substitution G A 5_prime_UTR_variant BLCA-CN 1 6215673 6215673 single base substitution G A exon_variant BLCA-CN 1 6215673 6215673 single base substitution G A synonymous_variant F164F 492C>T BLCA-US 1 6158568 6158568 single base substitution C T downstream_gene_variant BLCA-US 1 6173059 6173059 single base substitution C G splice_acceptor_variant BLCA-US 1 6181225 6181225 single base substitution G A 3_prime_UTR_variant BLCA-US 1 6181225 6181225 single base substitution G A downstream_gene_variant BLCA-US 1 6181225 6181225 single base substitution G A exon_variant BLCA-US 1 6181225 6181225 single base substitution G A stop_gained R1618* 4852C>T BLCA-US 1 6181225 6181225 single base substitution G A stop_gained R475* 1423C>T BLCA-US 1 6188917 6188917 single base substitution G C 3_prime_UTR_variant BLCA-US 1 6188917 6188917 single base substitution G C exon_variant BLCA-US 1 6188917 6188917 single base substitution G C intron_variant BLCA-US 1 6188917 6188917 single base substitution G C synonymous_variant L1200L 3600C>G BLCA-US 1 6188917 6188917 single base substitution G C synonymous_variant L57L 171C>G BLCA-US 1 6188917 6188917 single base substitution G C upstream_gene_variant BLCA-US 1 6189100 6189100 single base substitution C T 5_prime_UTR_variant BLCA-US 1 6189100 6189100 single base substitution C T exon_variant BLCA-US 1 6189100 6189100 single base substitution C T splice_region_variant BLCA-US 1 6189100 6189100 single base substitution C T synonymous_variant Q1139Q 3417G>A BLCA-US 1 6189100 6189100 single base substitution C T upstream_gene_variant BLCA-US 1 6195343 6195343 single base substitution G A 5_prime_UTR_variant BLCA-US 1 6195343 6195343 single base substitution G A exon_variant BLCA-US 1 6195343 6195343 single base substitution G A synonymous_variant N939N 2817C>T BLCA-US 1 6195343 6195343 single base substitution G A upstream_gene_variant BLCA-US 1 6196893 6196893 single base substitution G C 5_prime_UTR_premature_start_codon_gain_variant BLCA-US 1 6196893 6196893 single base substitution G C exon_variant BLCA-US 1 6196893 6196893 single base substitution G C synonymous_variant L823L 2469C>G BLCA-US 1 6206323 6206323 single base substitution C T 5_prime_UTR_variant BLCA-US 1 6206323 6206323 single base substitution C T exon_variant BLCA-US 1 6206323 6206323 single base substitution C T missense_variant R584H 1751G>A BLCA-US 1 6206323 6206323 single base substitution C T upstream_gene_variant BLCA-US 1 6214906 6214906 single base substitution C T 5_prime_UTR_variant BLCA-US 1 6214906 6214906 single base substitution C T exon_variant BLCA-US 1 6214906 6214906 single base substitution C T missense_variant V187I 559G>A BLCA-US 1 6219573 6219573 single base substitution C T splice_region_variant BOCA-FR 1 6232058 6232058 single base substitution G A intron_variant BRCA-EU 1 6157258 6157258 single base substitution G A downstream_gene_variant BRCA-EU 1 6158012 6158012 single base substitution C T downstream_gene_variant BRCA-EU 1 6158655 6158655 single base substitution C T downstream_gene_variant BRCA-EU 1 6159061 6159061 single base substitution G T downstream_gene_variant BRCA-EU 1 6159095 6159095 single base substitution T C downstream_gene_variant BRCA-EU 1 6160315 6160315 single base substitution C A downstream_gene_variant BRCA-EU 1 6161916 6161916 single base substitution G T 3_prime_UTR_variant BRCA-EU 1 6161916 6161916 single base substitution G T downstream_gene_variant BRCA-EU 1 6163382 6163382 single base substitution G A 3_prime_UTR_variant BRCA-EU 1 6163382 6163382 single base substitution G A downstream_gene_variant BRCA-EU 1 6163457 6163457 single base substitution G A 3_prime_UTR_variant BRCA-EU 1 6163457 6163457 single base substitution G A downstream_gene_variant BRCA-EU 1 6164239 6164239 single base substitution G A 3_prime_UTR_variant BRCA-EU 1 6164239 6164239 single base substitution G A downstream_gene_variant BRCA-EU 1 6165710 6165710 single base substitution G C intron_variant BRCA-EU 1 6167523 6167523 single base substitution G A intron_variant BRCA-EU 1 6167523 6167523 single base substitution G A upstream_gene_variant BRCA-EU 1 6168344 6168344 single base substitution G C intron_variant BRCA-EU 1 6168344 6168344 single base substitution G C upstream_gene_variant BRCA-EU 1 6169428 6169428 single base substitution C G intron_variant BRCA-EU 1 6169428 6169428 single base substitution C G upstream_gene_variant BRCA-EU 1 6170593 6170593 single base substitution G A splice_region_variant BRCA-EU 1 6170593 6170593 single base substitution G A upstream_gene_variant BRCA-EU 1 6171609 6171609 single base substitution A G intron_variant BRCA-EU 1 6171609 6171609 single base substitution A G upstream_gene_variant BRCA-EU 1 6172600 6172600 single base substitution T C intron_variant BRCA-EU 1 6173011 6173011 single base substitution T A 3_prime_UTR_variant BRCA-EU 1 6173011 6173011 single base substitution T A exon_variant BRCA-EU 1 6173011 6173011 single base substitution T A missense_variant S1654C 4960A>T BRCA-EU 1 6173011 6173011 single base substitution T A missense_variant S511C 1531A>T BRCA-EU 1 6173254 6173254 single base substitution C T intron_variant BRCA-EU 1 6174166 6174166 single base substitution A G intron_variant BRCA-EU 1 6176213 6176213 single base substitution A T intron_variant BRCA-EU 1 6176301 6176302 deletion of <=200bp AT - intron_variant BRCA-EU 1 6177405 6177405 single base substitution G A intron_variant BRCA-EU 1 6177547 6177547 single base substitution G C intron_variant BRCA-EU 1 6178138 6178138 single base substitution G T intron_variant BRCA-EU 1 6180772 6180772 single base substitution G A downstream_gene_variant BRCA-EU 1 6180772 6180772 single base substitution G A intron_variant BRCA-EU 1 6181392 6181392 single base substitution G A downstream_gene_variant BRCA-EU 1 6181392 6181392 single base substitution G A intron_variant BRCA-EU 1 6181470 6181470 single base substitution T G downstream_gene_variant BRCA-EU 1 6181470 6181470 single base substitution T G intron_variant BRCA-EU 1 6181785 6181785 single base substitution G A downstream_gene_variant BRCA-EU 1 6181785 6181785 single base substitution G A intron_variant BRCA-EU 1 6183043 6183043 single base substitution C T downstream_gene_variant BRCA-EU 1 6183043 6183043 single base substitution C T intron_variant BRCA-EU 1 6183213 6183213 single base substitution C T downstream_gene_variant BRCA-EU 1 6183213 6183213 single base substitution C T intron_variant BRCA-EU 1 6183650 6183650 single base substitution C G downstream_gene_variant BRCA-EU 1 6183650 6183650 single base substitution C G intron_variant BRCA-EU 1 6184145 6184145 single base substitution T A 3_prime_UTR_variant BRCA-EU 1 6184145 6184145 single base substitution T A downstream_gene_variant BRCA-EU 1 6184145 6184145 single base substitution T A exon_variant BRCA-EU 1 6184145 6184145 single base substitution T A intron_variant BRCA-EU 1 6184145 6184145 single base substitution T A missense_variant N1521I 4562A>T BRCA-EU 1 6184145 6184145 single base substitution T A missense_variant N378I 1133A>T BRCA-EU 1 6184923 6184923 single base substitution G A downstream_gene_variant BRCA-EU 1 6184923 6184923 single base substitution G A intron_variant BRCA-EU 1 6186364 6186364 single base substitution C A intron_variant BRCA-EU 1 6189215 6189215 single base substitution G A intron_variant BRCA-EU 1 6189215 6189215 single base substitution G A upstream_gene_variant BRCA-EU 1 6189305 6189305 single base substitution G A intron_variant BRCA-EU 1 6189305 6189305 single base substitution G A upstream_gene_variant BRCA-EU 1 6192616 6192616 single base substitution A T intron_variant BRCA-EU 1 6192616 6192616 single base substitution A T upstream_gene_variant BRCA-EU 1 6192773 6192773 single base substitution T C intron_variant BRCA-EU 1 6192773 6192773 single base substitution T C upstream_gene_variant BRCA-EU 1 6196771 6196771 single base substitution C T intron_variant BRCA-EU 1 6196771 6196771 single base substitution C T upstream_gene_variant BRCA-EU 1 6199357 6199357 single base substitution G T intron_variant BRCA-EU 1 6199897 6199897 single base substitution A T intron_variant BRCA-EU 1 6199995 6199995 single base substitution A T intron_variant BRCA-EU 1 6201344 6201344 single base substitution C T intron_variant BRCA-EU 1 6201365 6201365 insertion of <=200bp - TAA intron_variant BRCA-EU 1 6201406 6201406 single base substitution T C intron_variant BRCA-EU 1 6203040 6203040 single base substitution G T intron_variant BRCA-EU 1 6205551 6205551 single base substitution G A intron_variant BRCA-EU 1 6205551 6205551 single base substitution G A upstream_gene_variant BRCA-EU 1 6206324 6206324 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 1 6206324 6206324 single base substitution G A exon_variant BRCA-EU 1 6206324 6206324 single base substitution G A missense_variant R584C 1750C>T BRCA-EU 1 6206324 6206324 single base substitution G A upstream_gene_variant BRCA-EU 1 6209463 6209463 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 1 6209463 6209463 single base substitution C T exon_variant BRCA-EU 1 6209463 6209463 single base substitution C T missense_variant G335D 1004G>A BRCA-EU 1 6209641 6209641 single base substitution T C intron_variant BRCA-EU 1 6211909 6211909 single base substitution G A intron_variant BRCA-EU 1 6212401 6212401 single base substitution C A intron_variant BRCA-EU 1 6213715 6213715 single base substitution C A intron_variant BRCA-EU 1 6214919 6214919 single base substitution G T 5_prime_UTR_variant BRCA-EU 1 6214919 6214919 single base substitution G T exon_variant BRCA-EU 1 6214919 6214919 single base substitution G T synonymous_variant S182S 546C>A BRCA-EU 1 6214968 6214968 single base substitution G T intron_variant BRCA-EU 1 6215695 6215695 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 1 6215695 6215695 single base substitution G A exon_variant BRCA-EU 1 6215695 6215695 single base substitution G A missense_variant T157M 470C>T BRCA-EU 1 6215695 6215695 single base substitution G C 5_prime_UTR_variant BRCA-EU 1 6215695 6215695 single base substitution G C exon_variant BRCA-EU 1 6215695 6215695 single base substitution G C missense_variant T157R 470C>G BRCA-EU 1 6216758 6216758 single base substitution G C intron_variant BRCA-EU 1 6216787 6216787 single base substitution G T intron_variant BRCA-EU 1 6217919 6217919 single base substitution G C intron_variant BRCA-EU 1 6219952 6219952 single base substitution G T intron_variant BRCA-EU 1 6220976 6220976 single base substitution G A intron_variant BRCA-EU 1 6221745 6221745 single base substitution G A intron_variant BRCA-EU 1 6226545 6226545 single base substitution C T intron_variant BRCA-EU 1 6227695 6227695 single base substitution C T intron_variant BRCA-EU 1 6227898 6227898 single base substitution G A intron_variant BRCA-EU 1 6231376 6231376 single base substitution C T intron_variant BRCA-EU 1 6233693 6233693 single base substitution G C intron_variant BRCA-EU 1 6236426 6236426 single base substitution G C intron_variant BRCA-EU 1 6236869 6236869 single base substitution A T intron_variant BRCA-EU 1 6237317 6237317 single base substitution G C intron_variant BRCA-EU 1 6237511 6237511 single base substitution G A intron_variant BRCA-EU 1 6238595 6238595 single base substitution C T intron_variant BRCA-EU 1 6240385 6240385 deletion of <=200bp G - upstream_gene_variant BRCA-EU 1 6241078 6241081 deletion of <=200bp CTGT - upstream_gene_variant BRCA-EU 1 6242155 6242177 deletion of <=200bp TGGTGTCTGTCGTCAGGCTGGGG - upstream_gene_variant BRCA-EU 1 6242359 6242359 single base substitution A G upstream_gene_variant BRCA-EU 1 6242959 6242959 single base substitution C T upstream_gene_variant BRCA-EU 1 6244000 6244000 single base substitution C T upstream_gene_variant BRCA-FR 1 6160315 6160315 single base substitution C A downstream_gene_variant BRCA-FR 1 6162562 6162562 single base substitution C G 3_prime_UTR_variant BRCA-FR 1 6162562 6162562 single base substitution C G downstream_gene_variant BRCA-FR 1 6181785 6181785 single base substitution G A downstream_gene_variant BRCA-FR 1 6181785 6181785 single base substitution G A intron_variant BRCA-FR 1 6189215 6189215 single base substitution G A intron_variant BRCA-FR 1 6189215 6189215 single base substitution G A upstream_gene_variant BRCA-FR 1 6191131 6191131 single base substitution G C intron_variant BRCA-FR 1 6191131 6191131 single base substitution G C upstream_gene_variant BRCA-FR 1 6211224 6211224 single base substitution G A intron_variant BRCA-FR 1 6212440 6212440 single base substitution G A intron_variant BRCA-FR 1 6225804 6225804 single base substitution C T intron_variant BRCA-FR 1 6231044 6231044 single base substitution G T intron_variant BRCA-FR 1 6231376 6231376 single base substitution C T intron_variant BRCA-FR 1 6238595 6238595 single base substitution C T intron_variant BRCA-KR 1 6191601 6191601 single base substitution C G intron_variant BRCA-KR 1 6191601 6191601 single base substitution C G upstream_gene_variant BRCA-UK 1 6189078 6189078 single base substitution G A 3_prime_UTR_variant BRCA-UK 1 6189078 6189078 single base substitution G A exon_variant BRCA-UK 1 6189078 6189078 single base substitution G A intron_variant BRCA-UK 1 6189078 6189078 single base substitution G A missense_variant R1147C 3439C>T BRCA-UK 1 6189078 6189078 single base substitution G A missense_variant R4C 10C>T BRCA-UK 1 6189078 6189078 single base substitution G A upstream_gene_variant BRCA-UK 1 6211203 6211203 single base substitution C T 5_prime_UTR_variant BRCA-UK 1 6211203 6211203 single base substitution C T exon_variant BRCA-UK 1 6211203 6211203 single base substitution C T missense_variant E295K 883G>A BRCA-UK 1 6215747 6215747 single base substitution C T 5_prime_UTR_variant BRCA-UK 1 6215747 6215747 single base substitution C T exon_variant BRCA-UK 1 6215747 6215747 single base substitution C T missense_variant E140K 418G>A BRCA-US 1 6157368 6157368 insertion of <=200bp - G downstream_gene_variant BRCA-US 1 6166527 6166527 single base substitution G A 3_prime_UTR_variant BRCA-US 1 6166527 6166527 single base substitution G A intron_variant BRCA-US 1 6166527 6166527 single base substitution G A missense_variant P1929S 5785C>T BRCA-US 1 6169975 6169975 single base substitution G A 3_prime_UTR_variant BRCA-US 1 6169975 6169975 single base substitution G A missense_variant H1820Y 5458C>T BRCA-US 1 6169975 6169975 single base substitution G A missense_variant H677Y 2029C>T BRCA-US 1 6169975 6169975 single base substitution G A upstream_gene_variant BRCA-US 1 6172237 6172237 single base substitution G C 3_prime_UTR_variant BRCA-US 1 6172237 6172237 single base substitution G C missense_variant F1701L 5103C>G BRCA-US 1 6172237 6172237 single base substitution G C missense_variant F558L 1674C>G BRCA-US 1 6172263 6172263 single base substitution T C 3_prime_UTR_variant BRCA-US 1 6172263 6172263 single base substitution T C missense_variant K1693E 5077A>G BRCA-US 1 6172263 6172263 single base substitution T C missense_variant K550E 1648A>G BRCA-US 1 6181297 6181297 single base substitution C T downstream_gene_variant BRCA-US 1 6181297 6181297 single base substitution C T missense_variant A1594T 4780G>A BRCA-US 1 6181297 6181297 single base substitution C T missense_variant A451T 1351G>A BRCA-US 1 6181297 6181297 single base substitution C T splice_region_variant BRCA-US 1 6181593 6181593 single base substitution G T 3_prime_UTR_variant BRCA-US 1 6181593 6181593 single base substitution G T downstream_gene_variant BRCA-US 1 6181593 6181593 single base substitution G T exon_variant BRCA-US 1 6181593 6181593 single base substitution G T missense_variant D1580E 4740C>A BRCA-US 1 6181593 6181593 single base substitution G T missense_variant D437E 1311C>A BRCA-US 1 6185196 6185196 single base substitution A C 3_prime_UTR_variant BRCA-US 1 6185196 6185196 single base substitution A C downstream_gene_variant BRCA-US 1 6185196 6185196 single base substitution A C exon_variant BRCA-US 1 6185196 6185196 single base substitution A C intron_variant BRCA-US 1 6185196 6185196 single base substitution A C missense_variant V1453G 4358T>G BRCA-US 1 6185196 6185196 single base substitution A C missense_variant V310G 929T>G BRCA-US 1 6191719 6191719 single base substitution G T 5_prime_UTR_variant BRCA-US 1 6191719 6191719 single base substitution G T exon_variant BRCA-US 1 6191719 6191719 single base substitution G T synonymous_variant L1078L 3234C>A BRCA-US 1 6191719 6191719 single base substitution G T upstream_gene_variant BRCA-US 1 6191787 6191787 single base substitution G T 5_prime_UTR_premature_start_codon_gain_variant BRCA-US 1 6191787 6191787 single base substitution G T exon_variant BRCA-US 1 6191787 6191787 single base substitution G T missense_variant L1056M 3166C>A BRCA-US 1 6191787 6191787 single base substitution G T upstream_gene_variant BRCA-US 1 6194863 6194863 deletion of <=200bp C - 5_prime_UTR_variant BRCA-US 1 6194863 6194863 deletion of <=200bp C - exon_variant BRCA-US 1 6194863 6194863 deletion of <=200bp C - frameshift_variant G976 BRCA-US 1 6194863 6194863 deletion of <=200bp C - upstream_gene_variant BRCA-US 1 6194863 6194863 single base substitution C T 5_prime_UTR_variant BRCA-US 1 6194863 6194863 single base substitution C T exon_variant BRCA-US 1 6194863 6194863 single base substitution C T missense_variant G976D 2927G>A BRCA-US 1 6194863 6194863 single base substitution C T upstream_gene_variant BRCA-US 1 6195315 6195315 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant BRCA-US 1 6195315 6195315 single base substitution G A exon_variant BRCA-US 1 6195315 6195315 single base substitution G A missense_variant R949W 2845C>T BRCA-US 1 6195315 6195315 single base substitution G A upstream_gene_variant BRCA-US 1 6202309 6202309 single base substitution G A 5_prime_UTR_variant BRCA-US 1 6202309 6202309 single base substitution G A exon_variant BRCA-US 1 6202309 6202309 single base substitution G A missense_variant A772V 2315C>T BRCA-US 1 6202326 6202326 single base substitution G A 5_prime_UTR_variant BRCA-US 1 6202326 6202326 single base substitution G A exon_variant BRCA-US 1 6202326 6202326 single base substitution G A synonymous_variant R766R 2298C>T BRCA-US 1 6204082 6204082 single base substitution A C splice_donor_variant BRCA-US 1 6206325 6206325 single base substitution G A 5_prime_UTR_variant BRCA-US 1 6206325 6206325 single base substitution G A exon_variant BRCA-US 1 6206325 6206325 single base substitution G A synonymous_variant Y583Y 1749C>T BRCA-US 1 6206325 6206325 single base substitution G A upstream_gene_variant BRCA-US 1 6211099 6211099 single base substitution C A 5_prime_UTR_variant BRCA-US 1 6211099 6211099 single base substitution C A exon_variant BRCA-US 1 6211099 6211099 single base substitution C A missense_variant K329N 987G>T BRCA-US 1 6214772 6214772 insertion of <=200bp - G 5_prime_UTR_variant BRCA-US 1 6214772 6214772 insertion of <=200bp - G exon_variant BRCA-US 1 6214772 6214772 insertion of <=200bp - G frameshift_variant P231P? BRCA-US 1 6215763 6215763 single base substitution C T 5_prime_UTR_variant BRCA-US 1 6215763 6215763 single base substitution C T exon_variant BRCA-US 1 6215763 6215763 single base substitution C T synonymous_variant S134S 402G>A BTCA-JP 1 6166353 6166353 insertion of <=200bp - A splice_region_variant BTCA-JP 1 6170472 6170472 single base substitution G C 3_prime_UTR_variant BTCA-JP 1 6170472 6170472 single base substitution G C missense_variant F1788L 5364C>G BTCA-JP 1 6170472 6170472 single base substitution G C missense_variant F645L 1935C>G BTCA-JP 1 6170472 6170472 single base substitution G C upstream_gene_variant BTCA-JP 1 6172219 6172219 single base substitution G A 3_prime_UTR_variant BTCA-JP 1 6172219 6172219 single base substitution G A synonymous_variant I1707I 5121C>T BTCA-JP 1 6172219 6172219 single base substitution G A synonymous_variant I564I 1692C>T BTCA-JP 1 6173079 6173079 single base substitution G A intron_variant BTCA-JP 1 6181512 6181512 single base substitution C A downstream_gene_variant BTCA-JP 1 6181512 6181512 single base substitution C A intron_variant BTCA-JP 1 6184072 6184072 single base substitution C T 3_prime_UTR_variant BTCA-JP 1 6184072 6184072 single base substitution C T downstream_gene_variant BTCA-JP 1 6184072 6184072 single base substitution C T exon_variant BTCA-JP 1 6184072 6184072 single base substitution C T intron_variant BTCA-JP 1 6184072 6184072 single base substitution C T synonymous_variant S1545S 4635G>A BTCA-JP 1 6184072 6184072 single base substitution C T synonymous_variant S402S 1206G>A BTCA-JP 1 6184249 6184249 deletion of <=200bp G - downstream_gene_variant BTCA-JP 1 6184249 6184249 deletion of <=200bp G - intron_variant BTCA-JP 1 6186588 6186588 single base substitution C T intron_variant BTCA-JP 1 6188578 6188578 single base substitution C T 3_prime_UTR_variant BTCA-JP 1 6188578 6188578 single base substitution C T exon_variant BTCA-JP 1 6188578 6188578 single base substitution C T intron_variant BTCA-JP 1 6188578 6188578 single base substitution C T synonymous_variant K1237K 3711G>A BTCA-JP 1 6188578 6188578 single base substitution C T synonymous_variant K94K 282G>A BTCA-JP 1 6188702 6188702 single base substitution G A intron_variant BTCA-JP 1 6188702 6188702 single base substitution G A upstream_gene_variant BTCA-JP 1 6196874 6196874 single base substitution T C 5_prime_UTR_variant BTCA-JP 1 6196874 6196874 single base substitution T C exon_variant BTCA-JP 1 6196874 6196874 single base substitution T C missense_variant T830A 2488A>G BTCA-JP 1 6204294 6204294 single base substitution G A intron_variant BTCA-JP 1 6204294 6204294 single base substitution G A upstream_gene_variant BTCA-JP 1 6206903 6206903 single base substitution C T 5_prime_UTR_variant BTCA-JP 1 6206903 6206903 single base substitution C T exon_variant BTCA-JP 1 6206903 6206903 single base substitution C T missense_variant R471Q 1412G>A BTCA-JP 1 6206903 6206903 single base substitution C T upstream_gene_variant BTCA-JP 1 6212529 6212529 single base substitution C T 5_prime_UTR_variant BTCA-JP 1 6212529 6212529 single base substitution C T exon_variant BTCA-JP 1 6212529 6212529 single base substitution C T synonymous_variant T271T 813G>A BTCA-JP 1 6214775 6214775 single base substitution G T 5_prime_UTR_variant BTCA-JP 1 6214775 6214775 single base substitution G T exon_variant BTCA-JP 1 6214775 6214775 single base substitution G T synonymous_variant P230P 690C>A BTCA-JP 1 6214808 6214808 single base substitution C T 5_prime_UTR_variant BTCA-JP 1 6214808 6214808 single base substitution C T exon_variant BTCA-JP 1 6214808 6214808 single base substitution C T synonymous_variant T219T 657G>A CESC-US 1 6169958 6169958 single base substitution G C 3_prime_UTR_variant CESC-US 1 6169958 6169958 single base substitution G C synonymous_variant L1825L 5475C>G CESC-US 1 6169958 6169958 single base substitution G C synonymous_variant L682L 2046C>G CESC-US 1 6169958 6169958 single base substitution G C upstream_gene_variant CESC-US 1 6170487 6170487 single base substitution C T 3_prime_UTR_variant CESC-US 1 6170487 6170487 single base substitution C T synonymous_variant E1783E 5349G>A CESC-US 1 6170487 6170487 single base substitution C T synonymous_variant E640E 1920G>A CESC-US 1 6170487 6170487 single base substitution C T upstream_gene_variant CESC-US 1 6202574 6202574 single base substitution C T 5_prime_UTR_variant CESC-US 1 6202574 6202574 single base substitution C T exon_variant CESC-US 1 6202574 6202574 single base substitution C T missense_variant R712H 2135G>A CESC-US 1 6211203 6211203 single base substitution C T 5_prime_UTR_variant CESC-US 1 6211203 6211203 single base substitution C T exon_variant CESC-US 1 6211203 6211203 single base substitution C T missense_variant E295K 883G>A CESC-US 1 6214792 6214792 single base substitution G A 5_prime_UTR_variant CESC-US 1 6214792 6214792 single base substitution G A exon_variant CESC-US 1 6214792 6214792 single base substitution G A missense_variant P225S 673C>T CESC-US 1 6214952 6214952 single base substitution G C 5_prime_UTR_premature_start_codon_gain_variant CESC-US 1 6214952 6214952 single base substitution G C exon_variant CESC-US 1 6214952 6214952 single base substitution G C synonymous_variant L171L 513C>G CESC-US 1 6228322 6228322 insertion of <=200bp - CA 5_prime_UTR_variant CESC-US 1 6228322 6228322 insertion of <=200bp - CA exon_variant CESC-US 1 6228322 6228322 insertion of <=200bp - CA frameshift_variant G32G? CLLE-ES 1 6160695 6160695 insertion of <=200bp - A downstream_gene_variant CLLE-ES 1 6173281 6173281 single base substitution C T intron_variant CLLE-ES 1 6180749 6180749 single base substitution C A downstream_gene_variant CLLE-ES 1 6180749 6180749 single base substitution C A intron_variant CLLE-ES 1 6204568 6204568 single base substitution G A intron_variant CLLE-ES 1 6204568 6204568 single base substitution G A upstream_gene_variant CLLE-ES 1 6210127 6210127 single base substitution G A intron_variant CLLE-ES 1 6220080 6220080 single base substitution A G intron_variant CLLE-ES 1 6220317 6220317 single base substitution G A intron_variant CLLE-ES 1 6235548 6235548 single base substitution G A intron_variant CLLE-ES 1 6236910 6236910 single base substitution A T intron_variant COAD-US 1 6157383 6157383 single base substitution C T downstream_gene_variant COAD-US 1 6158582 6158582 single base substitution T G downstream_gene_variant COAD-US 1 6171834 6171834 single base substitution C T splice_donor_variant COAD-US 1 6184072 6184072 single base substitution C T 3_prime_UTR_variant COAD-US 1 6184072 6184072 single base substitution C T downstream_gene_variant COAD-US 1 6184072 6184072 single base substitution C T exon_variant COAD-US 1 6184072 6184072 single base substitution C T intron_variant COAD-US 1 6184072 6184072 single base substitution C T synonymous_variant S1545S 4635G>A COAD-US 1 6184072 6184072 single base substitution C T synonymous_variant S402S 1206G>A COAD-US 1 6184144 6184144 single base substitution G A 3_prime_UTR_variant COAD-US 1 6184144 6184144 single base substitution G A downstream_gene_variant COAD-US 1 6184144 6184144 single base substitution G A exon_variant COAD-US 1 6184144 6184144 single base substitution G A intron_variant COAD-US 1 6184144 6184144 single base substitution G A synonymous_variant N1521N 4563C>T COAD-US 1 6184144 6184144 single base substitution G A synonymous_variant N378N 1134C>T COAD-US 1 6184649 6184649 single base substitution G A 3_prime_UTR_variant COAD-US 1 6184649 6184649 single base substitution G A downstream_gene_variant COAD-US 1 6184649 6184649 single base substitution G A exon_variant COAD-US 1 6184649 6184649 single base substitution G A intron_variant COAD-US 1 6184649 6184649 single base substitution G A synonymous_variant G1489G 4467C>T COAD-US 1 6184649 6184649 single base substitution G A synonymous_variant G346G 1038C>T COAD-US 1 6184675 6184675 single base substitution C T 3_prime_UTR_variant COAD-US 1 6184675 6184675 single base substitution C T downstream_gene_variant COAD-US 1 6184675 6184675 single base substitution C T exon_variant COAD-US 1 6184675 6184675 single base substitution C T intron_variant COAD-US 1 6184675 6184675 single base substitution C T missense_variant D1481N 4441G>A COAD-US 1 6184675 6184675 single base substitution C T missense_variant D338N 1012G>A COAD-US 1 6185275 6185275 single base substitution G A 3_prime_UTR_variant COAD-US 1 6185275 6185275 single base substitution G A downstream_gene_variant COAD-US 1 6185275 6185275 single base substitution G A exon_variant COAD-US 1 6185275 6185275 single base substitution G A intron_variant COAD-US 1 6185275 6185275 single base substitution G A stop_gained R1427* 4279C>T COAD-US 1 6185275 6185275 single base substitution G A stop_gained R284* 850C>T COAD-US 1 6188947 6188947 single base substitution G A 3_prime_UTR_variant COAD-US 1 6188947 6188947 single base substitution G A exon_variant COAD-US 1 6188947 6188947 single base substitution G A intron_variant COAD-US 1 6188947 6188947 single base substitution G A synonymous_variant D1190D 3570C>T COAD-US 1 6188947 6188947 single base substitution G A synonymous_variant D47D 141C>T COAD-US 1 6188947 6188947 single base substitution G A upstream_gene_variant COAD-US 1 6189118 6189118 single base substitution G A 5_prime_UTR_variant COAD-US 1 6189118 6189118 single base substitution G A exon_variant COAD-US 1 6189118 6189118 single base substitution G A synonymous_variant R1133R 3399C>T COAD-US 1 6189118 6189118 single base substitution G A upstream_gene_variant COAD-US 1 6194862 6194862 insertion of <=200bp - C 5_prime_UTR_variant COAD-US 1 6194862 6194862 insertion of <=200bp - C exon_variant COAD-US 1 6194862 6194862 insertion of <=200bp - C frameshift_variant G976G? COAD-US 1 6194862 6194862 insertion of <=200bp - C upstream_gene_variant COAD-US 1 6195434 6195434 single base substitution G T 5_prime_UTR_premature_start_codon_gain_variant COAD-US 1 6195434 6195434 single base substitution G T exon_variant COAD-US 1 6195434 6195434 single base substitution G T missense_variant A909D 2726C>A COAD-US 1 6195434 6195434 single base substitution G T upstream_gene_variant COAD-US 1 6196811 6196811 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant COAD-US 1 6196811 6196811 single base substitution G A exon_variant COAD-US 1 6196811 6196811 single base substitution G A missense_variant R851C 2551C>T COAD-US 1 6202245 6202245 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant COAD-US 1 6202245 6202245 single base substitution G A exon_variant COAD-US 1 6202245 6202245 single base substitution G A synonymous_variant N793N 2379C>T COAD-US 1 6202356 6202356 single base substitution C T 5_prime_UTR_variant COAD-US 1 6202356 6202356 single base substitution C T exon_variant COAD-US 1 6202356 6202356 single base substitution C T synonymous_variant A756A 2268G>A COAD-US 1 6202629 6202629 single base substitution C T 5_prime_UTR_variant COAD-US 1 6202629 6202629 single base substitution C T exon_variant COAD-US 1 6202629 6202629 single base substitution C T missense_variant D694N 2080G>A COAD-US 1 6204161 6204161 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant COAD-US 1 6204161 6204161 single base substitution G A exon_variant COAD-US 1 6204161 6204161 single base substitution G A synonymous_variant Y619Y 1857C>T COAD-US 1 6204194 6204194 single base substitution C T 5_prime_UTR_variant COAD-US 1 6204194 6204194 single base substitution C T exon_variant COAD-US 1 6204194 6204194 single base substitution C T synonymous_variant V608V 1824G>A COAD-US 1 6204194 6204194 single base substitution C T upstream_gene_variant COAD-US 1 6209103 6209103 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant COAD-US 1 6209103 6209103 single base substitution G A exon_variant COAD-US 1 6209103 6209103 single base substitution G A synonymous_variant D398D 1194C>T COAD-US 1 6209103 6209103 single base substitution G A upstream_gene_variant COAD-US 1 6209363 6209363 single base substitution T C 5_prime_UTR_variant COAD-US 1 6209363 6209363 single base substitution T C exon_variant COAD-US 1 6209363 6209363 single base substitution T C synonymous_variant V368V 1104A>G COAD-US 1 6209392 6209392 single base substitution C T 5_prime_UTR_variant COAD-US 1 6209392 6209392 single base substitution C T exon_variant COAD-US 1 6209392 6209392 single base substitution C T missense_variant D359N 1075G>A COAD-US 1 6211183 6211183 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant COAD-US 1 6211183 6211183 single base substitution G A exon_variant COAD-US 1 6211183 6211183 single base substitution G A synonymous_variant F301F 903C>T COAD-US 1 6212530 6212530 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant COAD-US 1 6212530 6212530 single base substitution G A exon_variant COAD-US 1 6212530 6212530 single base substitution G A missense_variant T271M 812C>T COCA-CN 1 6158648 6158648 single base substitution G A downstream_gene_variant COCA-CN 1 6158691 6158691 single base substitution C T downstream_gene_variant COCA-CN 1 6165261 6165261 single base substitution T A 3_prime_UTR_variant COCA-CN 1 6166555 6166555 single base substitution G T 3_prime_UTR_variant COCA-CN 1 6166555 6166555 single base substitution G T intron_variant COCA-CN 1 6166555 6166555 single base substitution G T synonymous_variant S1919S 5757C>A COCA-CN 1 6166678 6166678 single base substitution G T missense_variant Q1914K 5740C>A COCA-CN 1 6166678 6166678 single base substitution G T missense_variant Q52K 154C>A COCA-CN 1 6166678 6166678 single base substitution G T missense_variant Q771K 2311C>A COCA-CN 1 6166678 6166678 single base substitution G T splice_region_variant COCA-CN 1 6172981 6172981 single base substitution C T 3_prime_UTR_variant COCA-CN 1 6172981 6172981 single base substitution C T missense_variant E1664K 4990G>A COCA-CN 1 6172981 6172981 single base substitution C T missense_variant E521K 1561G>A COCA-CN 1 6185064 6185064 single base substitution G A downstream_gene_variant COCA-CN 1 6185064 6185064 single base substitution G A intron_variant COCA-CN 1 6185108 6185108 single base substitution C T downstream_gene_variant COCA-CN 1 6185108 6185108 single base substitution C T intron_variant COCA-CN 1 6188377 6188377 single base substitution G A intron_variant COCA-CN 1 6188726 6188726 single base substitution C T intron_variant COCA-CN 1 6188726 6188726 single base substitution C T upstream_gene_variant COCA-CN 1 6190279 6190279 single base substitution C T 5_prime_UTR_variant COCA-CN 1 6190279 6190279 single base substitution C T exon_variant COCA-CN 1 6190279 6190279 single base substitution C T synonymous_variant P1124P 3372G>A COCA-CN 1 6190279 6190279 single base substitution C T upstream_gene_variant COCA-CN 1 6191689 6191689 single base substitution A G splice_donor_variant COCA-CN 1 6191689 6191689 single base substitution A G upstream_gene_variant COCA-CN 1 6191870 6191870 single base substitution C T intron_variant COCA-CN 1 6191870 6191870 single base substitution C T upstream_gene_variant COCA-CN 1 6194251 6194251 single base substitution C T 5_prime_UTR_variant COCA-CN 1 6194251 6194251 single base substitution C T exon_variant COCA-CN 1 6194251 6194251 single base substitution C T missense_variant M1027I 3081G>A COCA-CN 1 6194251 6194251 single base substitution C T upstream_gene_variant COCA-CN 1 6195266 6195266 single base substitution C A intron_variant COCA-CN 1 6195266 6195266 single base substitution C A upstream_gene_variant COCA-CN 1 6196779 6196779 single base substitution G A intron_variant COCA-CN 1 6196779 6196779 single base substitution G A upstream_gene_variant COCA-CN 1 6196956 6196956 single base substitution C T intron_variant COCA-CN 1 6202305 6202305 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant COCA-CN 1 6202305 6202305 single base substitution G A exon_variant COCA-CN 1 6202305 6202305 single base substitution G A synonymous_variant P773P 2319C>T COCA-CN 1 6202308 6202308 single base substitution C T 5_prime_UTR_variant COCA-CN 1 6202308 6202308 single base substitution C T exon_variant COCA-CN 1 6202308 6202308 single base substitution C T synonymous_variant A772A 2316G>A COCA-CN 1 6203940 6203940 single base substitution C A 5_prime_UTR_premature_start_codon_gain_variant COCA-CN 1 6203940 6203940 single base substitution C A exon_variant COCA-CN 1 6203940 6203940 single base substitution C A missense_variant K662N 1986G>T COCA-CN 1 6204247 6204247 single base substitution A G intron_variant COCA-CN 1 6204247 6204247 single base substitution A G upstream_gene_variant COCA-CN 1 6211156 6211156 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant COCA-CN 1 6211156 6211156 single base substitution G A exon_variant COCA-CN 1 6211156 6211156 single base substitution G A synonymous_variant S310S 930C>T COCA-CN 1 6212441 6212442 deletion of <=200bp CA - intron_variant COCA-CN 1 6215047 6215047 single base substitution A G intron_variant COCA-CN 1 6215048 6215048 single base substitution T C intron_variant COCA-CN 1 6228180 6228180 single base substitution A C intron_variant EOPC-DE 1 6167308 6167308 single base substitution A G intron_variant EOPC-DE 1 6167308 6167308 single base substitution A G upstream_gene_variant EOPC-DE 1 6204052 6204052 single base substitution C A intron_variant EOPC-DE 1 6217132 6217132 single base substitution C T intron_variant EOPC-DE 1 6220082 6220082 single base substitution A G intron_variant ESAD-UK 1 6158501 6158501 single base substitution G A downstream_gene_variant ESAD-UK 1 6159021 6159021 single base substitution C T downstream_gene_variant ESAD-UK 1 6160374 6160374 single base substitution C T downstream_gene_variant ESAD-UK 1 6161100 6161100 insertion of <=200bp - A downstream_gene_variant ESAD-UK 1 6161100 6161100 single base substitution T A downstream_gene_variant ESAD-UK 1 6162882 6162882 single base substitution C T 3_prime_UTR_variant ESAD-UK 1 6162882 6162882 single base substitution C T downstream_gene_variant ESAD-UK 1 6163176 6163176 single base substitution A C 3_prime_UTR_variant ESAD-UK 1 6163176 6163176 single base substitution A C downstream_gene_variant ESAD-UK 1 6164680 6164680 single base substitution C G 3_prime_UTR_variant ESAD-UK 1 6164680 6164680 single base substitution C G downstream_gene_variant ESAD-UK 1 6165521 6165521 single base substitution G A intron_variant ESAD-UK 1 6166441 6166441 single base substitution G A intron_variant ESAD-UK 1 6166521 6166521 single base substitution A T 3_prime_UTR_variant ESAD-UK 1 6166521 6166521 single base substitution A T intron_variant ESAD-UK 1 6166521 6166521 single base substitution A T missense_variant F1931I 5791T>A ESAD-UK 1 6167085 6167085 single base substitution A C intron_variant ESAD-UK 1 6167085 6167085 single base substitution A C upstream_gene_variant ESAD-UK 1 6167175 6167175 single base substitution C T intron_variant ESAD-UK 1 6167175 6167175 single base substitution C T upstream_gene_variant ESAD-UK 1 6167463 6167463 deletion of <=200bp G - intron_variant ESAD-UK 1 6167463 6167463 deletion of <=200bp G - upstream_gene_variant ESAD-UK 1 6167467 6167470 deletion of <=200bp AAAT - intron_variant ESAD-UK 1 6167467 6167470 deletion of <=200bp AAAT - upstream_gene_variant ESAD-UK 1 6168249 6168249 single base substitution A T intron_variant ESAD-UK 1 6168249 6168249 single base substitution A T upstream_gene_variant ESAD-UK 1 6168286 6168286 single base substitution G A intron_variant ESAD-UK 1 6168286 6168286 single base substitution G A upstream_gene_variant ESAD-UK 1 6169989 6169989 single base substitution G A 3_prime_UTR_variant ESAD-UK 1 6169989 6169989 single base substitution G A missense_variant T1815M 5444C>T ESAD-UK 1 6169989 6169989 single base substitution G A missense_variant T672M 2015C>T ESAD-UK 1 6169989 6169989 single base substitution G A upstream_gene_variant ESAD-UK 1 6171026 6171026 single base substitution G A intron_variant ESAD-UK 1 6171026 6171026 single base substitution G A upstream_gene_variant ESAD-UK 1 6171557 6171557 single base substitution A G intron_variant ESAD-UK 1 6171557 6171557 single base substitution A G upstream_gene_variant ESAD-UK 1 6173335 6173335 single base substitution T G intron_variant ESAD-UK 1 6173709 6173709 single base substitution C A intron_variant ESAD-UK 1 6173996 6173996 single base substitution A T intron_variant ESAD-UK 1 6173997 6173997 single base substitution C G intron_variant ESAD-UK 1 6174610 6174610 insertion of <=200bp - A intron_variant ESAD-UK 1 6175319 6175319 single base substitution A G intron_variant ESAD-UK 1 6175980 6175980 single base substitution T A intron_variant ESAD-UK 1 6178776 6178776 single base substitution A G intron_variant ESAD-UK 1 6179787 6179787 single base substitution G A intron_variant ESAD-UK 1 6179862 6179862 single base substitution C T intron_variant ESAD-UK 1 6181742 6181742 single base substitution C T downstream_gene_variant ESAD-UK 1 6181742 6181742 single base substitution C T intron_variant ESAD-UK 1 6182884 6182884 single base substitution C T downstream_gene_variant ESAD-UK 1 6182884 6182884 single base substitution C T intron_variant ESAD-UK 1 6185300 6185300 single base substitution G A downstream_gene_variant ESAD-UK 1 6185300 6185300 single base substitution G A intron_variant ESAD-UK 1 6185300 6185300 single base substitution G A splice_region_variant ESAD-UK 1 6185614 6185614 single base substitution C T 3_prime_UTR_variant ESAD-UK 1 6185614 6185614 single base substitution C T exon_variant ESAD-UK 1 6185614 6185614 single base substitution C T intron_variant ESAD-UK 1 6185614 6185614 single base substitution C T synonymous_variant P1410P 4230G>A ESAD-UK 1 6185614 6185614 single base substitution C T synonymous_variant P267P 801G>A ESAD-UK 1 6188331 6188331 single base substitution C T intron_variant ESAD-UK 1 6189245 6189245 single base substitution C T intron_variant ESAD-UK 1 6189245 6189245 single base substitution C T upstream_gene_variant ESAD-UK 1 6190291 6190291 single base substitution C T 5_prime_UTR_variant ESAD-UK 1 6190291 6190291 single base substitution C T exon_variant ESAD-UK 1 6190291 6190291 single base substitution C T synonymous_variant S1120S 3360G>A ESAD-UK 1 6190291 6190291 single base substitution C T upstream_gene_variant ESAD-UK 1 6190422 6190422 deletion of <=200bp G - intron_variant ESAD-UK 1 6190422 6190422 deletion of <=200bp G - upstream_gene_variant ESAD-UK 1 6190516 6190516 single base substitution G A intron_variant ESAD-UK 1 6190516 6190516 single base substitution G A upstream_gene_variant ESAD-UK 1 6190766 6190766 single base substitution C G intron_variant ESAD-UK 1 6190766 6190766 single base substitution C G upstream_gene_variant ESAD-UK 1 6193010 6193010 single base substitution A C intron_variant ESAD-UK 1 6193010 6193010 single base substitution A C upstream_gene_variant ESAD-UK 1 6193160 6193160 single base substitution G A intron_variant ESAD-UK 1 6193160 6193160 single base substitution G A upstream_gene_variant ESAD-UK 1 6193320 6193320 single base substitution G A intron_variant ESAD-UK 1 6193320 6193320 single base substitution G A upstream_gene_variant ESAD-UK 1 6194207 6194207 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant ESAD-UK 1 6194207 6194207 single base substitution C T exon_variant ESAD-UK 1 6194207 6194207 single base substitution C T missense_variant R1042H 3125G>A ESAD-UK 1 6194207 6194207 single base substitution C T upstream_gene_variant ESAD-UK 1 6194384 6194384 single base substitution G T intron_variant ESAD-UK 1 6194384 6194384 single base substitution G T upstream_gene_variant ESAD-UK 1 6194525 6194525 single base substitution C T intron_variant ESAD-UK 1 6194525 6194525 single base substitution C T upstream_gene_variant ESAD-UK 1 6194908 6194908 single base substitution T A 5_prime_UTR_premature_start_codon_gain_variant ESAD-UK 1 6194908 6194908 single base substitution T A exon_variant ESAD-UK 1 6194908 6194908 single base substitution T A missense_variant K961M 2882A>T ESAD-UK 1 6194908 6194908 single base substitution T A upstream_gene_variant ESAD-UK 1 6195219 6195219 single base substitution G A intron_variant ESAD-UK 1 6195219 6195219 single base substitution G A upstream_gene_variant ESAD-UK 1 6195269 6195269 single base substitution C T intron_variant ESAD-UK 1 6195269 6195269 single base substitution C T upstream_gene_variant ESAD-UK 1 6198785 6198785 single base substitution G T intron_variant ESAD-UK 1 6200229 6200229 single base substitution G A intron_variant ESAD-UK 1 6201155 6201155 single base substitution G C intron_variant ESAD-UK 1 6202296 6202296 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant ESAD-UK 1 6202296 6202296 single base substitution G A exon_variant ESAD-UK 1 6202296 6202296 single base substitution G A synonymous_variant Y776Y 2328C>T ESAD-UK 1 6202651 6202651 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant ESAD-UK 1 6202651 6202651 single base substitution G A exon_variant ESAD-UK 1 6202651 6202651 single base substitution G A synonymous_variant F686F 2058C>T ESAD-UK 1 6205218 6205218 single base substitution C T intron_variant ESAD-UK 1 6205218 6205218 single base substitution C T upstream_gene_variant ESAD-UK 1 6206323 6206323 single base substitution C T 5_prime_UTR_variant ESAD-UK 1 6206323 6206323 single base substitution C T exon_variant ESAD-UK 1 6206323 6206323 single base substitution C T missense_variant R584H 1751G>A ESAD-UK 1 6206323 6206323 single base substitution C T upstream_gene_variant ESAD-UK 1 6206456 6206456 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant ESAD-UK 1 6206456 6206456 single base substitution G A exon_variant ESAD-UK 1 6206456 6206456 single base substitution G A missense_variant R540C 1618C>T ESAD-UK 1 6206456 6206456 single base substitution G A upstream_gene_variant ESAD-UK 1 6208438 6208438 single base substitution G A intron_variant ESAD-UK 1 6208438 6208438 single base substitution G A upstream_gene_variant ESAD-UK 1 6210492 6210495 deletion of <=200bp GGAT - intron_variant ESAD-UK 1 6211059 6211059 single base substitution C A intron_variant ESAD-UK 1 6211947 6211947 single base substitution G T intron_variant ESAD-UK 1 6214396 6214396 single base substitution C T intron_variant ESAD-UK 1 6218216 6218216 single base substitution C G intron_variant ESAD-UK 1 6219478 6219478 insertion of <=200bp - TTC 5_prime_UTR_variant ESAD-UK 1 6219478 6219478 insertion of <=200bp - TTC disruptive_inframe_insertion K102KK ESAD-UK 1 6219478 6219478 insertion of <=200bp - TTC exon_variant ESAD-UK 1 6220082 6220082 single base substitution A G intron_variant ESAD-UK 1 6223795 6223795 single base substitution G A intron_variant ESAD-UK 1 6224332 6224332 single base substitution G T intron_variant ESAD-UK 1 6225529 6225529 single base substitution C T intron_variant ESAD-UK 1 6230624 6230624 single base substitution G C intron_variant ESAD-UK 1 6230747 6230747 single base substitution G A intron_variant ESAD-UK 1 6231568 6231568 deletion of <=200bp C - intron_variant ESAD-UK 1 6231568 6231568 insertion of <=200bp - C intron_variant ESAD-UK 1 6233067 6233067 single base substitution G A intron_variant ESAD-UK 1 6233878 6233878 single base substitution C T intron_variant ESAD-UK 1 6235878 6235878 single base substitution G T intron_variant ESAD-UK 1 6237862 6237862 single base substitution C T intron_variant ESAD-UK 1 6237863 6237863 single base substitution G A intron_variant ESAD-UK 1 6240385 6240385 deletion of <=200bp G - upstream_gene_variant ESAD-UK 1 6240650 6240650 single base substitution G A upstream_gene_variant ESAD-UK 1 6240824 6240824 single base substitution C A upstream_gene_variant ESAD-UK 1 6242212 6242212 single base substitution C T upstream_gene_variant ESAD-UK 1 6243883 6243883 single base substitution G A upstream_gene_variant ESAD-UK 1 6244208 6244208 single base substitution C T upstream_gene_variant ESCA-CN 1 6162407 6162407 single base substitution A G 3_prime_UTR_variant ESCA-CN 1 6162407 6162407 single base substitution A G downstream_gene_variant ESCA-CN 1 6165419 6165419 single base substitution C T 3_prime_UTR_variant ESCA-CN 1 6166774 6166774 single base substitution G A 3_prime_UTR_variant ESCA-CN 1 6166774 6166774 single base substitution G A synonymous_variant L1882L 5644C>T ESCA-CN 1 6166774 6166774 single base substitution G A synonymous_variant L20L 58C>T ESCA-CN 1 6166774 6166774 single base substitution G A synonymous_variant L739L 2215C>T ESCA-CN 1 6190315 6190315 single base substitution C T 5_prime_UTR_variant ESCA-CN 1 6190315 6190315 single base substitution C T exon_variant ESCA-CN 1 6190315 6190315 single base substitution C T synonymous_variant A1112A 3336G>A ESCA-CN 1 6190315 6190315 single base substitution C T upstream_gene_variant ESCA-CN 1 6202326 6202326 single base substitution G A 5_prime_UTR_variant ESCA-CN 1 6202326 6202326 single base substitution G A exon_variant ESCA-CN 1 6202326 6202326 single base substitution G A synonymous_variant R766R 2298C>T ESCA-CN 1 6202464 6202464 single base substitution G A intron_variant GACA-CN 1 6203923 6203923 single base substitution T C 5_prime_UTR_variant GACA-CN 1 6203923 6203923 single base substitution T C exon_variant GACA-CN 1 6203923 6203923 single base substitution T C missense_variant D668G 2003A>G GACA-CN 1 6204178 6204178 single base substitution A T 5_prime_UTR_variant GACA-CN 1 6204178 6204178 single base substitution A T exon_variant GACA-CN 1 6204178 6204178 single base substitution A T missense_variant W614R 1840T>A GACA-CN 1 6204178 6204178 single base substitution A T upstream_gene_variant GBM-US 1 6171855 6171855 single base substitution C T 3_prime_UTR_variant GBM-US 1 6171855 6171855 single base substitution C T stop_gained W1743* 5229G>A GBM-US 1 6171855 6171855 single base substitution C T stop_gained W600* 1800G>A GBM-US 1 6172293 6172293 single base substitution T G 3_prime_UTR_variant GBM-US 1 6172293 6172293 single base substitution T G missense_variant N1683H 5047A>C GBM-US 1 6172293 6172293 single base substitution T G missense_variant N540H 1618A>C GBM-US 1 6181182 6181182 single base substitution G A 3_prime_UTR_variant GBM-US 1 6181182 6181182 single base substitution G A downstream_gene_variant GBM-US 1 6181182 6181182 single base substitution G A exon_variant GBM-US 1 6181182 6181182 single base substitution G A missense_variant P1632L 4895C>T GBM-US 1 6181182 6181182 single base substitution G A missense_variant P489L 1466C>T GBM-US 1 6184051 6184051 single base substitution G C 3_prime_UTR_variant GBM-US 1 6184051 6184051 single base substitution G C downstream_gene_variant GBM-US 1 6184051 6184051 single base substitution G C exon_variant GBM-US 1 6184051 6184051 single base substitution G C intron_variant GBM-US 1 6184051 6184051 single base substitution G C synonymous_variant P1552P 4656C>G GBM-US 1 6184051 6184051 single base substitution G C synonymous_variant P409P 1227C>G GBM-US 1 6189033 6189033 single base substitution C A 3_prime_UTR_variant GBM-US 1 6189033 6189033 single base substitution C A exon_variant GBM-US 1 6189033 6189033 single base substitution C A intron_variant GBM-US 1 6189033 6189033 single base substitution C A missense_variant A1162S 3484G>T GBM-US 1 6189033 6189033 single base substitution C A missense_variant A19S 55G>T GBM-US 1 6189033 6189033 single base substitution C A upstream_gene_variant GBM-US 1 6189059 6189059 single base substitution G A 3_prime_UTR_variant GBM-US 1 6189059 6189059 single base substitution G A exon_variant GBM-US 1 6189059 6189059 single base substitution G A intron_variant GBM-US 1 6189059 6189059 single base substitution G A missense_variant S10L 29C>T GBM-US 1 6189059 6189059 single base substitution G A missense_variant S1153L 3458C>T GBM-US 1 6189059 6189059 single base substitution G A upstream_gene_variant GBM-US 1 6206730 6206730 single base substitution G C 5_prime_UTR_variant GBM-US 1 6206730 6206730 single base substitution G C exon_variant GBM-US 1 6206730 6206730 single base substitution G C missense_variant L529V 1585C>G GBM-US 1 6206730 6206730 single base substitution G C upstream_gene_variant GBM-US 1 6209438 6209438 single base substitution C T 5_prime_UTR_variant GBM-US 1 6209438 6209438 single base substitution C T exon_variant GBM-US 1 6209438 6209438 single base substitution C T synonymous_variant Q343Q 1029G>A KIRC-US 1 6157369 6157369 deletion of <=200bp G - downstream_gene_variant KIRC-US 1 6171886 6171886 single base substitution T C 3_prime_UTR_variant KIRC-US 1 6171886 6171886 single base substitution T C missense_variant Y1733C 5198A>G KIRC-US 1 6171886 6171886 single base substitution T C missense_variant Y590C 1769A>G KIRC-US 1 6208965 6208965 single base substitution G T 5_prime_UTR_variant KIRC-US 1 6208965 6208965 single base substitution G T exon_variant KIRC-US 1 6208965 6208965 single base substitution G T missense_variant N444K 1332C>A KIRC-US 1 6208965 6208965 single base substitution G T upstream_gene_variant KIRC-US 1 6212526 6212526 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant KIRC-US 1 6212526 6212526 single base substitution G A exon_variant KIRC-US 1 6212526 6212526 single base substitution G A synonymous_variant A272A 816C>T KIRC-US 1 6214898 6214898 single base substitution A C 5_prime_UTR_variant KIRC-US 1 6214898 6214898 single base substitution A C exon_variant KIRC-US 1 6214898 6214898 single base substitution A C synonymous_variant G189G 567T>G KIRC-US 1 6228284 6228284 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant KIRC-US 1 6228284 6228284 single base substitution C T exon_variant KIRC-US 1 6228284 6228284 single base substitution C T missense_variant V45M 133G>A KIRP-US 1 6204188 6204188 single base substitution G A 5_prime_UTR_variant KIRP-US 1 6204188 6204188 single base substitution G A exon_variant KIRP-US 1 6204188 6204188 single base substitution G A synonymous_variant Y610Y 1830C>T KIRP-US 1 6204188 6204188 single base substitution G A upstream_gene_variant LAML-KR 1 6184192 6184192 single base substitution A G downstream_gene_variant LAML-KR 1 6184192 6184192 single base substitution A G intron_variant LAML-KR 1 6186339 6186339 single base substitution C T intron_variant LAML-KR 1 6194347 6194347 single base substitution T G intron_variant LAML-KR 1 6194347 6194347 single base substitution T G upstream_gene_variant LAML-KR 1 6198046 6198046 single base substitution C T intron_variant LAML-KR 1 6220200 6220200 single base substitution C A intron_variant LAML-KR 1 6220208 6220208 single base substitution G A intron_variant LAML-KR 1 6235445 6235445 single base substitution G A intron_variant LAML-KR 1 6235450 6235450 single base substitution C A intron_variant LGG-US 1 6186737 6186737 single base substitution G A 3_prime_UTR_variant LGG-US 1 6186737 6186737 single base substitution G A exon_variant LGG-US 1 6186737 6186737 single base substitution G A intron_variant LGG-US 1 6186737 6186737 single base substitution G A missense_variant R1325W 3973C>T LGG-US 1 6186737 6186737 single base substitution G A missense_variant R182W 544C>T LGG-US 1 6202211 6202211 insertion of <=200bp - A 5_prime_UTR_variant LGG-US 1 6202211 6202211 insertion of <=200bp - A exon_variant LGG-US 1 6202211 6202211 insertion of <=200bp - A frameshift_variant G805V? LGG-US 1 6202326 6202326 single base substitution G A 5_prime_UTR_variant LGG-US 1 6202326 6202326 single base substitution G A exon_variant LGG-US 1 6202326 6202326 single base substitution G A synonymous_variant R766R 2298C>T LICA-CN 1 6157326 6157326 single base substitution C T downstream_gene_variant LICA-CN 1 6166573 6166573 single base substitution G C intron_variant LICA-CN 1 6166573 6166573 single base substitution G C splice_region_variant LICA-CN 1 6185196 6185196 single base substitution A T 3_prime_UTR_variant LICA-CN 1 6185196 6185196 single base substitution A T downstream_gene_variant LICA-CN 1 6185196 6185196 single base substitution A T exon_variant LICA-CN 1 6185196 6185196 single base substitution A T intron_variant LICA-CN 1 6185196 6185196 single base substitution A T missense_variant V1453E 4358T>A LICA-CN 1 6185196 6185196 single base substitution A T missense_variant V310E 929T>A LICA-CN 1 6188143 6188143 single base substitution T A 3_prime_UTR_variant LICA-CN 1 6188143 6188143 single base substitution T A exon_variant LICA-CN 1 6188143 6188143 single base substitution T A intron_variant LICA-CN 1 6188143 6188143 single base substitution T A missense_variant K1289M 3866A>T LICA-CN 1 6188143 6188143 single base substitution T A missense_variant K146M 437A>T LICA-CN 1 6190309 6190309 single base substitution A T 5_prime_UTR_variant LICA-CN 1 6190309 6190309 single base substitution A T exon_variant LICA-CN 1 6190309 6190309 single base substitution A T synonymous_variant T1114T 3342T>A LICA-CN 1 6190309 6190309 single base substitution A T upstream_gene_variant LICA-CN 1 6194814 6194814 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant LICA-CN 1 6194814 6194814 single base substitution G A exon_variant LICA-CN 1 6194814 6194814 single base substitution G A synonymous_variant C992C 2976C>T LICA-CN 1 6194814 6194814 single base substitution G A upstream_gene_variant LICA-CN 1 6206437 6206437 single base substitution T A 5_prime_UTR_variant LICA-CN 1 6206437 6206437 single base substitution T A exon_variant LICA-CN 1 6206437 6206437 single base substitution T A missense_variant N546I 1637A>T LICA-CN 1 6206437 6206437 single base substitution T A upstream_gene_variant LICA-CN 1 6215662 6215662 single base substitution A T 5_prime_UTR_variant LICA-CN 1 6215662 6215662 single base substitution A T exon_variant LICA-CN 1 6215662 6215662 single base substitution A T missense_variant L168H 503T>A LICA-FR 1 6162860 6162860 single base substitution A C 3_prime_UTR_variant LICA-FR 1 6162860 6162860 single base substitution A C downstream_gene_variant LICA-FR 1 6163659 6163659 single base substitution G T 3_prime_UTR_variant LICA-FR 1 6163659 6163659 single base substitution G T downstream_gene_variant LICA-FR 1 6164107 6164107 single base substitution C T 3_prime_UTR_variant LICA-FR 1 6164107 6164107 single base substitution C T downstream_gene_variant LICA-FR 1 6169919 6169919 single base substitution G A 3_prime_UTR_variant LICA-FR 1 6169919 6169919 single base substitution G A synonymous_variant S1838S 5514C>T LICA-FR 1 6169919 6169919 single base substitution G A synonymous_variant S695S 2085C>T LICA-FR 1 6169919 6169919 single base substitution G A upstream_gene_variant LICA-FR 1 6181183 6181183 single base substitution G T 3_prime_UTR_variant LICA-FR 1 6181183 6181183 single base substitution G T downstream_gene_variant LICA-FR 1 6181183 6181183 single base substitution G T exon_variant LICA-FR 1 6181183 6181183 single base substitution G T missense_variant P1632T 4894C>A LICA-FR 1 6181183 6181183 single base substitution G T missense_variant P489T 1465C>A LICA-FR 1 6202309 6202309 single base substitution G T 5_prime_UTR_variant LICA-FR 1 6202309 6202309 single base substitution G T exon_variant LICA-FR 1 6202309 6202309 single base substitution G T missense_variant A772E 2315C>A LICA-FR 1 6202473 6202473 single base substitution C T splice_donor_variant LICA-FR 1 6210357 6210357 single base substitution A T intron_variant LICA-FR 1 6212502 6212502 deletion of <=200bp C - 5_prime_UTR_variant LICA-FR 1 6212502 6212502 deletion of <=200bp C - exon_variant LICA-FR 1 6212502 6212502 deletion of <=200bp C - frameshift_variant G280 LICA-FR 1 6225051 6225051 single base substitution C T intron_variant LIHC-US 1 6188597 6188597 single base substitution G A 3_prime_UTR_variant LIHC-US 1 6188597 6188597 single base substitution G A exon_variant LIHC-US 1 6188597 6188597 single base substitution G A intron_variant LIHC-US 1 6188597 6188597 single base substitution G A missense_variant A1231V 3692C>T LIHC-US 1 6188597 6188597 single base substitution G A missense_variant A88V 263C>T LIHC-US 1 6196807 6196807 single base substitution A T 5_prime_UTR_variant LIHC-US 1 6196807 6196807 single base substitution A T exon_variant LIHC-US 1 6196807 6196807 single base substitution A T missense_variant L852H 2555T>A LIHC-US 1 6206301 6206301 single base substitution C T 5_prime_UTR_variant LIHC-US 1 6206301 6206301 single base substitution C T exon_variant LIHC-US 1 6206301 6206301 single base substitution C T stop_gained W591* 1773G>A LIHC-US 1 6206301 6206301 single base substitution C T upstream_gene_variant LINC-JP 1 6162012 6162012 single base substitution C G 3_prime_UTR_variant LINC-JP 1 6162012 6162012 single base substitution C G downstream_gene_variant LINC-JP 1 6162336 6162336 deletion of <=200bp A - 3_prime_UTR_variant LINC-JP 1 6162336 6162336 deletion of <=200bp A - downstream_gene_variant LINC-JP 1 6164192 6164192 single base substitution G A 3_prime_UTR_variant LINC-JP 1 6164192 6164192 single base substitution G A downstream_gene_variant LINC-JP 1 6166353 6166353 deletion of <=200bp A - splice_region_variant LINC-JP 1 6166405 6166405 single base substitution G T intron_variant LINC-JP 1 6166743 6166743 single base substitution A G 3_prime_UTR_variant LINC-JP 1 6166743 6166743 single base substitution A G missense_variant L1892P 5675T>C LINC-JP 1 6166743 6166743 single base substitution A G missense_variant L30P 89T>C LINC-JP 1 6166743 6166743 single base substitution A G missense_variant L749P 2246T>C LINC-JP 1 6170075 6170075 single base substitution C T intron_variant LINC-JP 1 6170075 6170075 single base substitution C T upstream_gene_variant LINC-JP 1 6181550 6181550 single base substitution A G downstream_gene_variant LINC-JP 1 6181550 6181550 single base substitution A G splice_region_variant LINC-JP 1 6186855 6186855 single base substitution C T intron_variant LINC-JP 1 6186895 6186895 single base substitution C A intron_variant LINC-JP 1 6187450 6187450 single base substitution G A intron_variant LINC-JP 1 6194892 6194892 single base substitution C T 5_prime_UTR_variant LINC-JP 1 6194892 6194892 single base substitution C T exon_variant LINC-JP 1 6194892 6194892 single base substitution C T synonymous_variant R966R 2898G>A LINC-JP 1 6194892 6194892 single base substitution C T upstream_gene_variant LINC-JP 1 6197091 6197091 single base substitution C T intron_variant LINC-JP 1 6202127 6202127 single base substitution G A intron_variant LINC-JP 1 6204225 6204225 single base substitution G A intron_variant LINC-JP 1 6204225 6204225 single base substitution G A upstream_gene_variant LINC-JP 1 6213658 6213658 single base substitution G A intron_variant LINC-JP 1 6214783 6214783 single base substitution C T 5_prime_UTR_variant LINC-JP 1 6214783 6214783 single base substitution C T exon_variant LINC-JP 1 6214783 6214783 single base substitution C T missense_variant V228I 682G>A LINC-JP 1 6215131 6215131 single base substitution G A intron_variant LINC-JP 1 6219288 6219288 single base substitution C A intron_variant LINC-JP 1 6219289 6219289 single base substitution A T intron_variant LINC-JP 1 6226672 6226672 single base substitution A G intron_variant LINC-JP 1 6238429 6238429 single base substitution A G intron_variant LINC-JP 1 6243824 6243824 single base substitution C T upstream_gene_variant LINC-JP 1 6244347 6244347 single base substitution A T upstream_gene_variant LIRI-JP 1 6162821 6162821 deletion of <=200bp T - 3_prime_UTR_variant LIRI-JP 1 6162821 6162821 deletion of <=200bp T - downstream_gene_variant LIRI-JP 1 6164793 6164793 deletion of <=200bp G - 3_prime_UTR_variant LIRI-JP 1 6164793 6164793 deletion of <=200bp G - downstream_gene_variant LIRI-JP 1 6165556 6165556 single base substitution G T intron_variant LIRI-JP 1 6169767 6169767 single base substitution C T intron_variant LIRI-JP 1 6169767 6169767 single base substitution C T upstream_gene_variant LIRI-JP 1 6169772 6169772 single base substitution A G intron_variant LIRI-JP 1 6169772 6169772 single base substitution A G upstream_gene_variant LIRI-JP 1 6174454 6174454 single base substitution T A intron_variant LIRI-JP 1 6175023 6175023 single base substitution G T intron_variant LIRI-JP 1 6175647 6175647 single base substitution G T intron_variant LIRI-JP 1 6177267 6177267 single base substitution C T intron_variant LIRI-JP 1 6180238 6180238 single base substitution A C intron_variant LIRI-JP 1 6181534 6181534 single base substitution G T downstream_gene_variant LIRI-JP 1 6181534 6181534 single base substitution G T intron_variant LIRI-JP 1 6185241 6185241 single base substitution C A 3_prime_UTR_variant LIRI-JP 1 6185241 6185241 single base substitution C A downstream_gene_variant LIRI-JP 1 6185241 6185241 single base substitution C A exon_variant LIRI-JP 1 6185241 6185241 single base substitution C A intron_variant LIRI-JP 1 6185241 6185241 single base substitution C A missense_variant R1438L 4313G>T LIRI-JP 1 6185241 6185241 single base substitution C A missense_variant R295L 884G>T LIRI-JP 1 6185681 6185681 single base substitution C A intron_variant LIRI-JP 1 6189675 6189676 deletion of <=200bp TG - intron_variant LIRI-JP 1 6189675 6189676 deletion of <=200bp TG - upstream_gene_variant LIRI-JP 1 6190915 6190915 single base substitution G A intron_variant LIRI-JP 1 6190915 6190915 single base substitution G A upstream_gene_variant LIRI-JP 1 6191807 6191807 single base substitution A C missense_variant M1049R 3146T>G LIRI-JP 1 6191807 6191807 single base substitution A C splice_region_variant LIRI-JP 1 6191807 6191807 single base substitution A C upstream_gene_variant LIRI-JP 1 6191912 6191912 single base substitution A G intron_variant LIRI-JP 1 6191912 6191912 single base substitution A G upstream_gene_variant LIRI-JP 1 6192666 6192666 single base substitution C G intron_variant LIRI-JP 1 6192666 6192666 single base substitution C G upstream_gene_variant LIRI-JP 1 6192787 6192787 single base substitution C A intron_variant LIRI-JP 1 6192787 6192787 single base substitution C A upstream_gene_variant LIRI-JP 1 6194214 6194214 single base substitution C A 5_prime_UTR_variant LIRI-JP 1 6194214 6194214 single base substitution C A exon_variant LIRI-JP 1 6194214 6194214 single base substitution C A missense_variant G1040W 3118G>T LIRI-JP 1 6194214 6194214 single base substitution C A upstream_gene_variant LIRI-JP 1 6195260 6195260 single base substitution A G intron_variant LIRI-JP 1 6195260 6195260 single base substitution A G upstream_gene_variant LIRI-JP 1 6198137 6198137 single base substitution T G intron_variant LIRI-JP 1 6198801 6198801 single base substitution C T intron_variant LIRI-JP 1 6202078 6202078 single base substitution C T intron_variant LIRI-JP 1 6205056 6205056 single base substitution T C intron_variant LIRI-JP 1 6205056 6205056 single base substitution T C upstream_gene_variant LIRI-JP 1 6206269 6206269 single base substitution C A splice_region_variant LIRI-JP 1 6206269 6206269 single base substitution C A upstream_gene_variant LIRI-JP 1 6206366 6206366 single base substitution T C 5_prime_UTR_variant LIRI-JP 1 6206366 6206366 single base substitution T C exon_variant LIRI-JP 1 6206366 6206366 single base substitution T C missense_variant N570D 1708A>G LIRI-JP 1 6206366 6206366 single base substitution T C upstream_gene_variant LIRI-JP 1 6206763 6206763 single base substitution G T 5_prime_UTR_premature_start_codon_gain_variant LIRI-JP 1 6206763 6206763 single base substitution G T exon_variant LIRI-JP 1 6206763 6206763 single base substitution G T missense_variant L518M 1552C>A LIRI-JP 1 6206763 6206763 single base substitution G T upstream_gene_variant LIRI-JP 1 6206764 6206764 single base substitution C T 5_prime_UTR_variant LIRI-JP 1 6206764 6206764 single base substitution C T exon_variant LIRI-JP 1 6206764 6206764 single base substitution C T synonymous_variant G517G 1551G>A LIRI-JP 1 6206764 6206764 single base substitution C T upstream_gene_variant LIRI-JP 1 6206846 6206846 single base substitution C A 5_prime_UTR_variant LIRI-JP 1 6206846 6206846 single base substitution C A exon_variant LIRI-JP 1 6206846 6206846 single base substitution C A missense_variant G490V 1469G>T LIRI-JP 1 6206846 6206846 single base substitution C A upstream_gene_variant LIRI-JP 1 6208172 6208172 single base substitution C T intron_variant LIRI-JP 1 6208172 6208172 single base substitution C T upstream_gene_variant LIRI-JP 1 6211586 6211586 single base substitution C T intron_variant LIRI-JP 1 6212715 6212715 single base substitution G A intron_variant LIRI-JP 1 6212797 6212797 single base substitution G A intron_variant LIRI-JP 1 6213148 6213148 single base substitution G A intron_variant LIRI-JP 1 6217001 6217001 single base substitution T C intron_variant LIRI-JP 1 6217146 6217146 single base substitution A G intron_variant LIRI-JP 1 6219933 6219933 single base substitution T C intron_variant LIRI-JP 1 6221853 6221853 single base substitution A G intron_variant LIRI-JP 1 6228939 6228939 single base substitution C T intron_variant LIRI-JP 1 6230088 6230088 single base substitution G A intron_variant LIRI-JP 1 6237624 6237624 single base substitution G A intron_variant LIRI-JP 1 6238617 6238617 single base substitution G A intron_variant LIRI-JP 1 6241814 6241814 single base substitution G A upstream_gene_variant LIRI-JP 1 6242573 6242573 single base substitution T C upstream_gene_variant LIRI-JP 1 6242615 6242620 deletion of <=200bp GAGCTC - upstream_gene_variant LIRI-JP 1 6243039 6243039 single base substitution T A upstream_gene_variant LIRI-JP 1 6245179 6245179 single base substitution T C upstream_gene_variant LUSC-KR 1 6156971 6156971 single base substitution G A downstream_gene_variant LUSC-KR 1 6159660 6159660 single base substitution A G downstream_gene_variant LUSC-KR 1 6162601 6162601 single base substitution T C 3_prime_UTR_variant LUSC-KR 1 6162601 6162601 single base substitution T C downstream_gene_variant LUSC-KR 1 6163529 6163529 single base substitution C A 3_prime_UTR_variant LUSC-KR 1 6163529 6163529 single base substitution C A downstream_gene_variant LUSC-KR 1 6164029 6164029 single base substitution C T 3_prime_UTR_variant LUSC-KR 1 6164029 6164029 single base substitution C T downstream_gene_variant LUSC-KR 1 6164898 6164898 single base substitution C A 3_prime_UTR_variant LUSC-KR 1 6164898 6164898 single base substitution C A downstream_gene_variant LUSC-KR 1 6165306 6165306 single base substitution G T 3_prime_UTR_variant LUSC-KR 1 6168630 6168630 single base substitution G A intron_variant LUSC-KR 1 6168630 6168630 single base substitution G A upstream_gene_variant LUSC-KR 1 6168759 6168759 single base substitution G C intron_variant LUSC-KR 1 6168759 6168759 single base substitution G C upstream_gene_variant LUSC-KR 1 6171998 6171998 single base substitution G A intron_variant LUSC-KR 1 6172751 6172751 single base substitution C A intron_variant LUSC-KR 1 6174136 6174136 single base substitution C A intron_variant LUSC-KR 1 6176580 6176580 single base substitution G C intron_variant LUSC-KR 1 6177425 6177425 single base substitution G T intron_variant LUSC-KR 1 6178211 6178211 single base substitution G T intron_variant LUSC-KR 1 6178583 6178583 single base substitution G T intron_variant LUSC-KR 1 6180581 6180581 single base substitution T A intron_variant LUSC-KR 1 6182364 6182364 single base substitution G T downstream_gene_variant LUSC-KR 1 6182364 6182364 single base substitution G T intron_variant LUSC-KR 1 6183926 6183926 single base substitution T C downstream_gene_variant LUSC-KR 1 6183926 6183926 single base substitution T C intron_variant LUSC-KR 1 6191632 6191632 single base substitution C T intron_variant LUSC-KR 1 6191632 6191632 single base substitution C T upstream_gene_variant LUSC-KR 1 6195024 6195024 single base substitution C T intron_variant LUSC-KR 1 6195024 6195024 single base substitution C T upstream_gene_variant LUSC-KR 1 6195446 6195446 single base substitution A T 5_prime_UTR_variant LUSC-KR 1 6195446 6195446 single base substitution A T exon_variant LUSC-KR 1 6195446 6195446 single base substitution A T missense_variant L905Q 2714T>A LUSC-KR 1 6195446 6195446 single base substitution A T upstream_gene_variant LUSC-KR 1 6196951 6196951 single base substitution T A intron_variant LUSC-KR 1 6203334 6203334 single base substitution C A intron_variant LUSC-KR 1 6203335 6203335 single base substitution C A intron_variant LUSC-KR 1 6204222 6204222 single base substitution C G splice_region_variant LUSC-KR 1 6204222 6204222 single base substitution C G upstream_gene_variant LUSC-KR 1 6209020 6209020 single base substitution C T 5_prime_UTR_variant LUSC-KR 1 6209020 6209020 single base substitution C T exon_variant LUSC-KR 1 6209020 6209020 single base substitution C T missense_variant G426D 1277G>A LUSC-KR 1 6209020 6209020 single base substitution C T upstream_gene_variant LUSC-KR 1 6209265 6209265 single base substitution G T intron_variant LUSC-KR 1 6210531 6210531 single base substitution C T intron_variant LUSC-KR 1 6212355 6212355 single base substitution C T intron_variant LUSC-KR 1 6213571 6213571 single base substitution G A intron_variant LUSC-KR 1 6214599 6214599 single base substitution C A intron_variant LUSC-KR 1 6214701 6214701 single base substitution C A intron_variant LUSC-KR 1 6215540 6215540 single base substitution C A intron_variant LUSC-KR 1 6215979 6215979 single base substitution C A intron_variant LUSC-KR 1 6216134 6216134 single base substitution G T intron_variant LUSC-KR 1 6220082 6220082 single base substitution A G intron_variant LUSC-KR 1 6220200 6220200 single base substitution C A intron_variant LUSC-KR 1 6220208 6220208 single base substitution G A intron_variant LUSC-KR 1 6220354 6220354 single base substitution A G intron_variant LUSC-KR 1 6224151 6224151 single base substitution C A intron_variant LUSC-KR 1 6224368 6224368 single base substitution G A intron_variant LUSC-KR 1 6226847 6226847 single base substitution C G intron_variant LUSC-KR 1 6228180 6228180 single base substitution A C intron_variant LUSC-KR 1 6230898 6230898 single base substitution G A intron_variant LUSC-KR 1 6233145 6233145 single base substitution G T intron_variant LUSC-KR 1 6234455 6234455 single base substitution A G intron_variant LUSC-KR 1 6235445 6235445 single base substitution G A intron_variant LUSC-KR 1 6235775 6235775 single base substitution C T intron_variant LUSC-KR 1 6243258 6243258 single base substitution C A upstream_gene_variant LUSC-KR 1 6244709 6244709 single base substitution T C upstream_gene_variant LUSC-US 1 6169927 6169927 single base substitution C T 3_prime_UTR_variant LUSC-US 1 6169927 6169927 single base substitution C T missense_variant A1836T 5506G>A LUSC-US 1 6169927 6169927 single base substitution C T missense_variant A693T 2077G>A LUSC-US 1 6169927 6169927 single base substitution C T upstream_gene_variant LUSC-US 1 6169932 6169932 single base substitution C T 3_prime_UTR_variant LUSC-US 1 6169932 6169932 single base substitution C T missense_variant C1834Y 5501G>A LUSC-US 1 6169932 6169932 single base substitution C T missense_variant C691Y 2072G>A LUSC-US 1 6169932 6169932 single base substitution C T upstream_gene_variant LUSC-US 1 6170001 6170001 single base substitution T C 3_prime_UTR_variant LUSC-US 1 6170001 6170001 single base substitution T C missense_variant Y1811C 5432A>G LUSC-US 1 6170001 6170001 single base substitution T C missense_variant Y668C 2003A>G LUSC-US 1 6170001 6170001 single base substitution T C upstream_gene_variant LUSC-US 1 6185836 6185836 single base substitution C T 3_prime_UTR_variant LUSC-US 1 6185836 6185836 single base substitution C T exon_variant LUSC-US 1 6185836 6185836 single base substitution C T intron_variant LUSC-US 1 6185836 6185836 single base substitution C T synonymous_variant P1387P 4161G>A LUSC-US 1 6185836 6185836 single base substitution C T synonymous_variant P244P 732G>A LUSC-US 1 6194301 6194301 single base substitution T C 5_prime_UTR_variant LUSC-US 1 6194301 6194301 single base substitution T C exon_variant LUSC-US 1 6194301 6194301 single base substitution T C missense_variant N1011D 3031A>G LUSC-US 1 6194301 6194301 single base substitution T C upstream_gene_variant LUSC-US 1 6196587 6196587 single base substitution C A 5_prime_UTR_variant LUSC-US 1 6196587 6196587 single base substitution C A exon_variant LUSC-US 1 6196587 6196587 single base substitution C A stop_gained E896* 2686G>T LUSC-US 1 6196587 6196587 single base substitution C A upstream_gene_variant LUSC-US 1 6196612 6196612 single base substitution G A 5_prime_UTR_variant LUSC-US 1 6196612 6196612 single base substitution G A exon_variant LUSC-US 1 6196612 6196612 single base substitution G A synonymous_variant F887F 2661C>T LUSC-US 1 6196612 6196612 single base substitution G A upstream_gene_variant LUSC-US 1 6202587 6202587 single base substitution G A 5_prime_UTR_variant LUSC-US 1 6202587 6202587 single base substitution G A exon_variant LUSC-US 1 6202587 6202587 single base substitution G A missense_variant L708F 2122C>T LUSC-US 1 6202664 6202664 single base substitution G A missense_variant P682L 2045C>T LUSC-US 1 6202664 6202664 single base substitution G A splice_region_variant LUSC-US 1 6206373 6206373 single base substitution C A 5_prime_UTR_variant LUSC-US 1 6206373 6206373 single base substitution C A exon_variant LUSC-US 1 6206373 6206373 single base substitution C A missense_variant K567N 1701G>T LUSC-US 1 6206373 6206373 single base substitution C A upstream_gene_variant LUSC-US 1 6206386 6206386 deletion of <=200bp C - 5_prime_UTR_variant LUSC-US 1 6206386 6206386 deletion of <=200bp C - exon_variant LUSC-US 1 6206386 6206386 deletion of <=200bp C - frameshift_variant G563 LUSC-US 1 6206386 6206386 deletion of <=200bp C - upstream_gene_variant LUSC-US 1 6212538 6212538 single base substitution C T 5_prime_UTR_variant LUSC-US 1 6212538 6212538 single base substitution C T exon_variant LUSC-US 1 6212538 6212538 single base substitution C T synonymous_variant G268G 804G>A MALY-DE 1 6164671 6164671 single base substitution A G 3_prime_UTR_variant MALY-DE 1 6164671 6164671 single base substitution A G downstream_gene_variant MALY-DE 1 6167746 6167746 single base substitution T G intron_variant MALY-DE 1 6167746 6167746 single base substitution T G upstream_gene_variant MALY-DE 1 6167756 6167756 single base substitution G T intron_variant MALY-DE 1 6167756 6167756 single base substitution G T upstream_gene_variant MALY-DE 1 6167793 6167793 single base substitution G T intron_variant MALY-DE 1 6167793 6167793 single base substitution G T upstream_gene_variant MALY-DE 1 6168439 6168439 single base substitution G A intron_variant MALY-DE 1 6168439 6168439 single base substitution G A upstream_gene_variant MALY-DE 1 6174423 6174423 single base substitution C T intron_variant MALY-DE 1 6175138 6175138 single base substitution C T intron_variant MALY-DE 1 6175499 6175499 single base substitution A T intron_variant MALY-DE 1 6198076 6198076 single base substitution C G intron_variant MALY-DE 1 6208729 6208729 single base substitution C T intron_variant MALY-DE 1 6208729 6208729 single base substitution C T upstream_gene_variant MALY-DE 1 6219288 6219289 deletion of <=200bp CA - intron_variant MALY-DE 1 6220399 6220399 insertion of <=200bp - AGA intron_variant MALY-DE 1 6221079 6221079 single base substitution G A intron_variant MALY-DE 1 6221610 6221610 single base substitution C T intron_variant MALY-DE 1 6222502 6222502 single base substitution C T intron_variant MALY-DE 1 6226967 6226967 single base substitution C T intron_variant MALY-DE 1 6230589 6230589 single base substitution G A intron_variant MALY-DE 1 6235610 6235610 single base substitution G A intron_variant MALY-DE 1 6242221 6242221 single base substitution G A upstream_gene_variant MELA-AU 1 6157484 6157484 single base substitution C T downstream_gene_variant MELA-AU 1 6158060 6158060 single base substitution G A downstream_gene_variant MELA-AU 1 6158547 6158547 single base substitution C T downstream_gene_variant MELA-AU 1 6158574 6158574 single base substitution C T downstream_gene_variant MELA-AU 1 6158671 6158671 single base substitution C T downstream_gene_variant MELA-AU 1 6158784 6158784 single base substitution C T downstream_gene_variant MELA-AU 1 6158948 6158948 single base substitution C T downstream_gene_variant MELA-AU 1 6159105 6159105 single base substitution C G downstream_gene_variant MELA-AU 1 6159159 6159159 single base substitution T A downstream_gene_variant MELA-AU 1 6159193 6159193 single base substitution G A downstream_gene_variant MELA-AU 1 6160142 6160142 single base substitution C T downstream_gene_variant MELA-AU 1 6160347 6160347 single base substitution C T downstream_gene_variant MELA-AU 1 6160501 6160501 single base substitution C G downstream_gene_variant MELA-AU 1 6160557 6160557 single base substitution C T downstream_gene_variant MELA-AU 1 6160589 6160589 single base substitution C T downstream_gene_variant MELA-AU 1 6160983 6160983 single base substitution C T downstream_gene_variant MELA-AU 1 6161232 6161233 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 1 6161390 6161390 single base substitution G A downstream_gene_variant MELA-AU 1 6161429 6161429 single base substitution G A downstream_gene_variant MELA-AU 1 6162199 6162199 single base substitution C T 3_prime_UTR_variant MELA-AU 1 6162199 6162199 single base substitution C T downstream_gene_variant MELA-AU 1 6162539 6162539 single base substitution C T 3_prime_UTR_variant MELA-AU 1 6162539 6162539 single base substitution C T downstream_gene_variant MELA-AU 1 6163215 6163215 single base substitution A G 3_prime_UTR_variant MELA-AU 1 6163215 6163215 single base substitution A G downstream_gene_variant MELA-AU 1 6163739 6163739 single base substitution T C 3_prime_UTR_variant MELA-AU 1 6163739 6163739 single base substitution T C downstream_gene_variant MELA-AU 1 6163763 6163763 single base substitution C T 3_prime_UTR_variant MELA-AU 1 6163763 6163763 single base substitution C T downstream_gene_variant MELA-AU 1 6163838 6163838 single base substitution G A 3_prime_UTR_variant MELA-AU 1 6163838 6163838 single base substitution G A downstream_gene_variant MELA-AU 1 6164163 6164163 single base substitution G A 3_prime_UTR_variant MELA-AU 1 6164163 6164163 single base substitution G A downstream_gene_variant MELA-AU 1 6164441 6164441 single base substitution C T 3_prime_UTR_variant MELA-AU 1 6164441 6164441 single base substitution C T downstream_gene_variant MELA-AU 1 6164457 6164457 single base substitution C T 3_prime_UTR_variant MELA-AU 1 6164457 6164457 single base substitution C T downstream_gene_variant MELA-AU 1 6164546 6164546 single base substitution G A 3_prime_UTR_variant MELA-AU 1 6164546 6164546 single base substitution G A downstream_gene_variant MELA-AU 1 6164863 6164863 single base substitution C T 3_prime_UTR_variant MELA-AU 1 6164863 6164863 single base substitution C T downstream_gene_variant MELA-AU 1 6164880 6164880 single base substitution G A 3_prime_UTR_variant MELA-AU 1 6164880 6164880 single base substitution G A downstream_gene_variant MELA-AU 1 6164881 6164881 single base substitution G A 3_prime_UTR_variant MELA-AU 1 6164881 6164881 single base substitution G A downstream_gene_variant MELA-AU 1 6164898 6164898 single base substitution C T 3_prime_UTR_variant MELA-AU 1 6164898 6164898 single base substitution C T downstream_gene_variant MELA-AU 1 6164917 6164917 single base substitution G A 3_prime_UTR_variant MELA-AU 1 6164917 6164917 single base substitution G A downstream_gene_variant MELA-AU 1 6165152 6165152 single base substitution C T 3_prime_UTR_variant MELA-AU 1 6165282 6165282 single base substitution G A 3_prime_UTR_variant MELA-AU 1 6165973 6165973 single base substitution C T intron_variant MELA-AU 1 6166135 6166135 single base substitution G A intron_variant MELA-AU 1 6166561 6166561 single base substitution G A 3_prime_UTR_variant MELA-AU 1 6166561 6166561 single base substitution G A intron_variant MELA-AU 1 6166561 6166561 single base substitution G A synonymous_variant F1917F 5751C>T MELA-AU 1 6166647 6166647 single base substitution C T intron_variant MELA-AU 1 6166665 6166665 single base substitution C T intron_variant MELA-AU 1 6166682 6166682 single base substitution G A 3_prime_UTR_variant MELA-AU 1 6166682 6166682 single base substitution G A synonymous_variant I1912I 5736C>T MELA-AU 1 6166682 6166682 single base substitution G A synonymous_variant I50I 150C>T MELA-AU 1 6166682 6166682 single base substitution G A synonymous_variant I769I 2307C>T MELA-AU 1 6167059 6167059 single base substitution G A intron_variant MELA-AU 1 6167059 6167059 single base substitution G A upstream_gene_variant MELA-AU 1 6167259 6167259 single base substitution G A intron_variant MELA-AU 1 6167259 6167259 single base substitution G A upstream_gene_variant MELA-AU 1 6167263 6167263 single base substitution G A intron_variant MELA-AU 1 6167263 6167263 single base substitution G A upstream_gene_variant MELA-AU 1 6167304 6167304 single base substitution G A intron_variant MELA-AU 1 6167304 6167304 single base substitution G A upstream_gene_variant MELA-AU 1 6167316 6167316 single base substitution G A intron_variant MELA-AU 1 6167316 6167316 single base substitution G A upstream_gene_variant MELA-AU 1 6167381 6167381 single base substitution G A intron_variant MELA-AU 1 6167381 6167381 single base substitution G A upstream_gene_variant MELA-AU 1 6167440 6167440 single base substitution G A intron_variant MELA-AU 1 6167440 6167440 single base substitution G A upstream_gene_variant MELA-AU 1 6167525 6167525 single base substitution G A intron_variant MELA-AU 1 6167525 6167525 single base substitution G A upstream_gene_variant MELA-AU 1 6167664 6167664 single base substitution T G intron_variant MELA-AU 1 6167664 6167664 single base substitution T G upstream_gene_variant MELA-AU 1 6167739 6167739 single base substitution G A intron_variant MELA-AU 1 6167739 6167739 single base substitution G A upstream_gene_variant MELA-AU 1 6167899 6167899 single base substitution G A intron_variant MELA-AU 1 6167899 6167899 single base substitution G A upstream_gene_variant MELA-AU 1 6168030 6168030 single base substitution G A intron_variant MELA-AU 1 6168030 6168030 single base substitution G A upstream_gene_variant MELA-AU 1 6168049 6168049 single base substitution G A intron_variant MELA-AU 1 6168049 6168049 single base substitution G A upstream_gene_variant MELA-AU 1 6168064 6168064 single base substitution G A intron_variant MELA-AU 1 6168064 6168064 single base substitution G A upstream_gene_variant MELA-AU 1 6168081 6168081 single base substitution G A intron_variant MELA-AU 1 6168081 6168081 single base substitution G A upstream_gene_variant MELA-AU 1 6168101 6168101 single base substitution G A intron_variant MELA-AU 1 6168101 6168101 single base substitution G A upstream_gene_variant MELA-AU 1 6168113 6168113 single base substitution G A intron_variant MELA-AU 1 6168113 6168113 single base substitution G A upstream_gene_variant MELA-AU 1 6168141 6168141 single base substitution G A intron_variant MELA-AU 1 6168141 6168141 single base substitution G A upstream_gene_variant MELA-AU 1 6168160 6168160 single base substitution G A intron_variant MELA-AU 1 6168160 6168160 single base substitution G A upstream_gene_variant MELA-AU 1 6168178 6168178 single base substitution G A intron_variant MELA-AU 1 6168178 6168178 single base substitution G A upstream_gene_variant MELA-AU 1 6168225 6168225 single base substitution G A intron_variant MELA-AU 1 6168225 6168225 single base substitution G A upstream_gene_variant MELA-AU 1 6168248 6168248 single base substitution G A intron_variant MELA-AU 1 6168248 6168248 single base substitution G A upstream_gene_variant MELA-AU 1 6168264 6168264 single base substitution G A intron_variant MELA-AU 1 6168264 6168264 single base substitution G A upstream_gene_variant MELA-AU 1 6168439 6168439 single base substitution G A intron_variant MELA-AU 1 6168439 6168439 single base substitution G A upstream_gene_variant MELA-AU 1 6168444 6168444 single base substitution G A intron_variant MELA-AU 1 6168444 6168444 single base substitution G A upstream_gene_variant MELA-AU 1 6168630 6168630 single base substitution G A intron_variant MELA-AU 1 6168630 6168630 single base substitution G A upstream_gene_variant MELA-AU 1 6168771 6168771 single base substitution G A intron_variant MELA-AU 1 6168771 6168771 single base substitution G A upstream_gene_variant MELA-AU 1 6168789 6168789 single base substitution G A intron_variant MELA-AU 1 6168789 6168789 single base substitution G A upstream_gene_variant MELA-AU 1 6169069 6169069 single base substitution G A intron_variant MELA-AU 1 6169069 6169069 single base substitution G A upstream_gene_variant MELA-AU 1 6169291 6169291 single base substitution G A intron_variant MELA-AU 1 6169291 6169291 single base substitution G A upstream_gene_variant MELA-AU 1 6169307 6169307 single base substitution G A intron_variant MELA-AU 1 6169307 6169307 single base substitution G A upstream_gene_variant MELA-AU 1 6169813 6169813 single base substitution G A intron_variant MELA-AU 1 6169813 6169813 single base substitution G A upstream_gene_variant MELA-AU 1 6170026 6170026 single base substitution C T 3_prime_UTR_variant MELA-AU 1 6170026 6170026 single base substitution C T missense_variant E1803K 5407G>A MELA-AU 1 6170026 6170026 single base substitution C T missense_variant E660K 1978G>A MELA-AU 1 6170026 6170026 single base substitution C T upstream_gene_variant MELA-AU 1 6170060 6170060 single base substitution G A intron_variant MELA-AU 1 6170060 6170060 single base substitution G A upstream_gene_variant MELA-AU 1 6170416 6170417 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 1 6170416 6170417 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 1 6170472 6170472 single base substitution G A 3_prime_UTR_variant MELA-AU 1 6170472 6170472 single base substitution G A synonymous_variant F1788F 5364C>T MELA-AU 1 6170472 6170472 single base substitution G A synonymous_variant F645F 1935C>T MELA-AU 1 6170472 6170472 single base substitution G A upstream_gene_variant MELA-AU 1 6170590 6170590 single base substitution G A splice_region_variant MELA-AU 1 6170590 6170590 single base substitution G A upstream_gene_variant MELA-AU 1 6170890 6170890 single base substitution G A intron_variant MELA-AU 1 6170890 6170890 single base substitution G A upstream_gene_variant MELA-AU 1 6171217 6171217 single base substitution G A intron_variant MELA-AU 1 6171217 6171217 single base substitution G A upstream_gene_variant MELA-AU 1 6171386 6171386 single base substitution G A intron_variant MELA-AU 1 6171386 6171386 single base substitution G A upstream_gene_variant MELA-AU 1 6171597 6171597 single base substitution A G intron_variant MELA-AU 1 6171597 6171597 single base substitution A G upstream_gene_variant MELA-AU 1 6171646 6171646 single base substitution G A intron_variant MELA-AU 1 6171646 6171646 single base substitution G A upstream_gene_variant MELA-AU 1 6171698 6171698 single base substitution G A intron_variant MELA-AU 1 6171698 6171698 single base substitution G A upstream_gene_variant MELA-AU 1 6171734 6171734 single base substitution G A intron_variant MELA-AU 1 6171734 6171734 single base substitution G A upstream_gene_variant MELA-AU 1 6171806 6171806 single base substitution C T intron_variant MELA-AU 1 6171806 6171806 single base substitution C T upstream_gene_variant MELA-AU 1 6171884 6171884 single base substitution C T 3_prime_UTR_variant MELA-AU 1 6171884 6171884 single base substitution C T missense_variant D1734N 5200G>A MELA-AU 1 6171884 6171884 single base substitution C T missense_variant D591N 1771G>A MELA-AU 1 6172217 6172217 single base substitution G A 3_prime_UTR_variant MELA-AU 1 6172217 6172217 single base substitution G A missense_variant A1708V 5123C>T MELA-AU 1 6172217 6172217 single base substitution G A missense_variant A565V 1694C>T MELA-AU 1 6172264 6172264 single base substitution C T 3_prime_UTR_variant MELA-AU 1 6172264 6172264 single base substitution C T synonymous_variant G1692G 5076G>A MELA-AU 1 6172264 6172264 single base substitution C T synonymous_variant G549G 1647G>A MELA-AU 1 6172529 6172529 single base substitution C T intron_variant MELA-AU 1 6172530 6172530 single base substitution C T intron_variant MELA-AU 1 6172711 6172711 single base substitution C T intron_variant MELA-AU 1 6172872 6172872 single base substitution G A intron_variant MELA-AU 1 6173304 6173304 single base substitution G A intron_variant MELA-AU 1 6173371 6173371 single base substitution C T intron_variant MELA-AU 1 6173371 6173371 single base substitution C T splice_region_variant MELA-AU 1 6173467 6173467 single base substitution G A exon_variant MELA-AU 1 6173467 6173467 single base substitution G A intron_variant MELA-AU 1 6173526 6173526 single base substitution G A intron_variant MELA-AU 1 6173750 6173750 single base substitution G A intron_variant MELA-AU 1 6173751 6173751 single base substitution G A intron_variant MELA-AU 1 6173940 6173940 single base substitution C T intron_variant MELA-AU 1 6174004 6174004 single base substitution C T intron_variant MELA-AU 1 6174208 6174208 single base substitution G A intron_variant MELA-AU 1 6174319 6174319 single base substitution A T intron_variant MELA-AU 1 6174328 6174328 single base substitution C T intron_variant MELA-AU 1 6174790 6174790 single base substitution G A intron_variant MELA-AU 1 6174969 6174969 single base substitution G A intron_variant MELA-AU 1 6174973 6174973 single base substitution C T intron_variant MELA-AU 1 6175053 6175053 single base substitution G A intron_variant MELA-AU 1 6175195 6175195 single base substitution A G intron_variant MELA-AU 1 6175349 6175349 single base substitution A G intron_variant MELA-AU 1 6175442 6175442 single base substitution G A intron_variant MELA-AU 1 6175466 6175466 single base substitution G A intron_variant MELA-AU 1 6175543 6175543 single base substitution C T intron_variant MELA-AU 1 6175762 6175762 single base substitution T A intron_variant MELA-AU 1 6175877 6175877 single base substitution C T intron_variant MELA-AU 1 6176019 6176019 single base substitution G A intron_variant MELA-AU 1 6176111 6176111 single base substitution A G intron_variant MELA-AU 1 6176195 6176195 single base substitution T C intron_variant MELA-AU 1 6176374 6176374 single base substitution C T intron_variant MELA-AU 1 6176636 6176636 single base substitution C T intron_variant MELA-AU 1 6176891 6176891 single base substitution G A intron_variant MELA-AU 1 6177023 6177023 single base substitution C T intron_variant MELA-AU 1 6177225 6177225 single base substitution G A intron_variant MELA-AU 1 6177267 6177267 single base substitution C T intron_variant MELA-AU 1 6177331 6177331 single base substitution G A intron_variant MELA-AU 1 6177407 6177407 single base substitution G A intron_variant MELA-AU 1 6177425 6177425 single base substitution G A intron_variant MELA-AU 1 6177605 6177605 single base substitution C T intron_variant MELA-AU 1 6177621 6177621 single base substitution A T intron_variant MELA-AU 1 6177634 6177634 single base substitution G A intron_variant MELA-AU 1 6177740 6177740 single base substitution G A intron_variant MELA-AU 1 6177972 6177972 single base substitution G A intron_variant MELA-AU 1 6178166 6178166 single base substitution G A intron_variant MELA-AU 1 6178212 6178212 single base substitution G A intron_variant MELA-AU 1 6178224 6178224 single base substitution C T intron_variant MELA-AU 1 6178228 6178228 single base substitution G A intron_variant MELA-AU 1 6178263 6178264 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 1 6178276 6178276 single base substitution G A intron_variant MELA-AU 1 6178321 6178321 single base substitution C T intron_variant MELA-AU 1 6178340 6178340 single base substitution A G intron_variant MELA-AU 1 6178349 6178349 single base substitution G A intron_variant MELA-AU 1 6178787 6178787 single base substitution C T intron_variant MELA-AU 1 6179365 6179365 single base substitution C T intron_variant MELA-AU 1 6179926 6179926 single base substitution T A intron_variant MELA-AU 1 6180136 6180136 single base substitution G A intron_variant MELA-AU 1 6180910 6180910 single base substitution C T downstream_gene_variant MELA-AU 1 6180910 6180910 single base substitution C T intron_variant MELA-AU 1 6180911 6180911 single base substitution C T downstream_gene_variant MELA-AU 1 6180911 6180911 single base substitution C T intron_variant MELA-AU 1 6181025 6181025 single base substitution C T downstream_gene_variant MELA-AU 1 6181025 6181025 single base substitution C T intron_variant MELA-AU 1 6181056 6181056 single base substitution C T downstream_gene_variant MELA-AU 1 6181056 6181056 single base substitution C T intron_variant MELA-AU 1 6181134 6181134 single base substitution C T downstream_gene_variant MELA-AU 1 6181134 6181134 single base substitution C T intron_variant MELA-AU 1 6181311 6181311 single base substitution G A downstream_gene_variant MELA-AU 1 6181311 6181311 single base substitution G A intron_variant MELA-AU 1 6181359 6181359 single base substitution G A downstream_gene_variant MELA-AU 1 6181359 6181359 single base substitution G A intron_variant MELA-AU 1 6181439 6181439 single base substitution G A downstream_gene_variant MELA-AU 1 6181439 6181439 single base substitution G A intron_variant MELA-AU 1 6181471 6181471 single base substitution C T downstream_gene_variant MELA-AU 1 6181471 6181471 single base substitution C T intron_variant MELA-AU 1 6181548 6181548 single base substitution C T downstream_gene_variant MELA-AU 1 6181548 6181548 single base substitution C T splice_region_variant MELA-AU 1 6181682 6181682 single base substitution G A downstream_gene_variant MELA-AU 1 6181682 6181682 single base substitution G A intron_variant MELA-AU 1 6181707 6181707 single base substitution G A downstream_gene_variant MELA-AU 1 6181707 6181707 single base substitution G A intron_variant MELA-AU 1 6181878 6181878 single base substitution G A downstream_gene_variant MELA-AU 1 6181878 6181878 single base substitution G A intron_variant MELA-AU 1 6182024 6182024 single base substitution C T downstream_gene_variant MELA-AU 1 6182024 6182024 single base substitution C T intron_variant MELA-AU 1 6182951 6182951 single base substitution G A downstream_gene_variant MELA-AU 1 6182951 6182951 single base substitution G A intron_variant MELA-AU 1 6183012 6183012 single base substitution C T downstream_gene_variant MELA-AU 1 6183012 6183012 single base substitution C T intron_variant MELA-AU 1 6183318 6183318 single base substitution G A downstream_gene_variant MELA-AU 1 6183318 6183318 single base substitution G A intron_variant MELA-AU 1 6183464 6183464 single base substitution G A downstream_gene_variant MELA-AU 1 6183464 6183464 single base substitution G A intron_variant MELA-AU 1 6183836 6183836 single base substitution C T downstream_gene_variant MELA-AU 1 6183836 6183836 single base substitution C T intron_variant MELA-AU 1 6183905 6183905 single base substitution G A downstream_gene_variant MELA-AU 1 6183905 6183905 single base substitution G A intron_variant MELA-AU 1 6183984 6183984 single base substitution C T downstream_gene_variant MELA-AU 1 6183984 6183984 single base substitution C T intron_variant MELA-AU 1 6184011 6184011 single base substitution G A 3_prime_UTR_variant MELA-AU 1 6184011 6184011 single base substitution G A downstream_gene_variant MELA-AU 1 6184011 6184011 single base substitution G A exon_variant MELA-AU 1 6184011 6184011 single base substitution G A intron_variant MELA-AU 1 6184011 6184011 single base substitution G A missense_variant P1566S 4696C>T MELA-AU 1 6184011 6184011 single base substitution G A missense_variant P423S 1267C>T MELA-AU 1 6184141 6184141 single base substitution C T 3_prime_UTR_variant MELA-AU 1 6184141 6184141 single base substitution C T downstream_gene_variant MELA-AU 1 6184141 6184141 single base substitution C T exon_variant MELA-AU 1 6184141 6184141 single base substitution C T intron_variant MELA-AU 1 6184141 6184141 single base substitution C T synonymous_variant G1522G 4566G>A MELA-AU 1 6184141 6184141 single base substitution C T synonymous_variant G379G 1137G>A MELA-AU 1 6184164 6184164 single base substitution G A 3_prime_UTR_variant MELA-AU 1 6184164 6184164 single base substitution G A downstream_gene_variant MELA-AU 1 6184164 6184164 single base substitution G A exon_variant MELA-AU 1 6184164 6184164 single base substitution G A intron_variant MELA-AU 1 6184164 6184164 single base substitution G A stop_gained Q1515* 4543C>T MELA-AU 1 6184164 6184164 single base substitution G A stop_gained Q372* 1114C>T MELA-AU 1 6184252 6184252 single base substitution G A downstream_gene_variant MELA-AU 1 6184252 6184252 single base substitution G A intron_variant MELA-AU 1 6184658 6184658 single base substitution G A 3_prime_UTR_variant MELA-AU 1 6184658 6184658 single base substitution G A downstream_gene_variant MELA-AU 1 6184658 6184658 single base substitution G A exon_variant MELA-AU 1 6184658 6184658 single base substitution G A intron_variant MELA-AU 1 6184658 6184658 single base substitution G A synonymous_variant F1486F 4458C>T MELA-AU 1 6184658 6184658 single base substitution G A synonymous_variant F343F 1029C>T MELA-AU 1 6184863 6184863 single base substitution G A downstream_gene_variant MELA-AU 1 6184863 6184863 single base substitution G A intron_variant MELA-AU 1 6184889 6184889 single base substitution G A downstream_gene_variant MELA-AU 1 6184889 6184889 single base substitution G A intron_variant MELA-AU 1 6184929 6184929 single base substitution C T downstream_gene_variant MELA-AU 1 6184929 6184929 single base substitution C T intron_variant MELA-AU 1 6185264 6185264 single base substitution C T 3_prime_UTR_variant MELA-AU 1 6185264 6185264 single base substitution C T downstream_gene_variant MELA-AU 1 6185264 6185264 single base substitution C T exon_variant MELA-AU 1 6185264 6185264 single base substitution C T intron_variant MELA-AU 1 6185264 6185264 single base substitution C T synonymous_variant K1430K 4290G>A MELA-AU 1 6185264 6185264 single base substitution C T synonymous_variant K287K 861G>A MELA-AU 1 6185331 6185331 single base substitution G A downstream_gene_variant MELA-AU 1 6185331 6185331 single base substitution G A intron_variant MELA-AU 1 6185384 6185384 single base substitution G A downstream_gene_variant MELA-AU 1 6185384 6185384 single base substitution G A intron_variant MELA-AU 1 6185407 6185407 single base substitution G A downstream_gene_variant MELA-AU 1 6185407 6185407 single base substitution G A intron_variant MELA-AU 1 6185527 6185527 single base substitution C T downstream_gene_variant MELA-AU 1 6185527 6185527 single base substitution C T intron_variant MELA-AU 1 6186057 6186057 single base substitution C T intron_variant MELA-AU 1 6186146 6186146 single base substitution G A intron_variant MELA-AU 1 6186245 6186245 single base substitution C T intron_variant MELA-AU 1 6186252 6186252 single base substitution C T intron_variant MELA-AU 1 6186364 6186365 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 1 6186686 6186686 single base substitution C T 3_prime_UTR_variant MELA-AU 1 6186686 6186686 single base substitution C T exon_variant MELA-AU 1 6186686 6186686 single base substitution C T intron_variant MELA-AU 1 6186686 6186686 single base substitution C T missense_variant G1342S 4024G>A MELA-AU 1 6186686 6186686 single base substitution C T missense_variant G199S 595G>A MELA-AU 1 6186909 6186909 single base substitution A T intron_variant MELA-AU 1 6186912 6186912 single base substitution G A intron_variant MELA-AU 1 6187089 6187089 single base substitution C T intron_variant MELA-AU 1 6187653 6187653 single base substitution G A intron_variant MELA-AU 1 6188665 6188665 single base substitution C T 3_prime_UTR_variant MELA-AU 1 6188665 6188665 single base substitution C T exon_variant MELA-AU 1 6188665 6188665 single base substitution C T intron_variant MELA-AU 1 6188665 6188665 single base substitution C T missense_variant M1208I 3624G>A MELA-AU 1 6188665 6188665 single base substitution C T missense_variant M65I 195G>A MELA-AU 1 6188665 6188665 single base substitution C T upstream_gene_variant MELA-AU 1 6189106 6189106 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 1 6189106 6189106 single base substitution G A exon_variant MELA-AU 1 6189106 6189106 single base substitution G A synonymous_variant I1137I 3411C>T MELA-AU 1 6189106 6189106 single base substitution G A upstream_gene_variant MELA-AU 1 6189250 6189250 single base substitution G A intron_variant MELA-AU 1 6189250 6189250 single base substitution G A upstream_gene_variant MELA-AU 1 6189313 6189313 single base substitution C T intron_variant MELA-AU 1 6189313 6189313 single base substitution C T upstream_gene_variant MELA-AU 1 6189347 6189347 single base substitution G A intron_variant MELA-AU 1 6189347 6189347 single base substitution G A upstream_gene_variant MELA-AU 1 6189564 6189564 single base substitution C T intron_variant MELA-AU 1 6189564 6189564 single base substitution C T upstream_gene_variant MELA-AU 1 6189813 6189813 single base substitution C T intron_variant MELA-AU 1 6189813 6189813 single base substitution C T upstream_gene_variant MELA-AU 1 6189922 6189922 single base substitution C T intron_variant MELA-AU 1 6189922 6189922 single base substitution C T upstream_gene_variant MELA-AU 1 6189930 6189930 single base substitution C T intron_variant MELA-AU 1 6189930 6189930 single base substitution C T upstream_gene_variant MELA-AU 1 6189937 6189937 single base substitution C T intron_variant MELA-AU 1 6189937 6189937 single base substitution C T upstream_gene_variant MELA-AU 1 6190013 6190013 single base substitution C T intron_variant MELA-AU 1 6190013 6190013 single base substitution C T upstream_gene_variant MELA-AU 1 6190422 6190422 deletion of <=200bp G - intron_variant MELA-AU 1 6190422 6190422 deletion of <=200bp G - upstream_gene_variant MELA-AU 1 6190467 6190467 single base substitution G A intron_variant MELA-AU 1 6190467 6190467 single base substitution G A upstream_gene_variant MELA-AU 1 6190566 6190566 single base substitution G A intron_variant MELA-AU 1 6190566 6190566 single base substitution G A upstream_gene_variant MELA-AU 1 6190653 6190653 single base substitution A G intron_variant MELA-AU 1 6190653 6190653 single base substitution A G upstream_gene_variant MELA-AU 1 6190814 6190815 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 1 6190814 6190815 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 1 6191016 6191016 single base substitution C T intron_variant MELA-AU 1 6191016 6191016 single base substitution C T upstream_gene_variant MELA-AU 1 6191197 6191197 single base substitution G A intron_variant MELA-AU 1 6191197 6191197 single base substitution G A upstream_gene_variant MELA-AU 1 6191200 6191200 single base substitution G A intron_variant MELA-AU 1 6191200 6191200 single base substitution G A upstream_gene_variant MELA-AU 1 6191232 6191233 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 1 6191232 6191233 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 1 6191237 6191237 single base substitution G C intron_variant MELA-AU 1 6191237 6191237 single base substitution G C upstream_gene_variant MELA-AU 1 6191251 6191251 single base substitution G A intron_variant MELA-AU 1 6191251 6191251 single base substitution G A upstream_gene_variant MELA-AU 1 6191339 6191339 single base substitution G A intron_variant MELA-AU 1 6191339 6191339 single base substitution G A upstream_gene_variant MELA-AU 1 6191506 6191506 single base substitution C T intron_variant MELA-AU 1 6191506 6191506 single base substitution C T upstream_gene_variant MELA-AU 1 6191544 6191544 single base substitution A C intron_variant MELA-AU 1 6191544 6191544 single base substitution A C upstream_gene_variant MELA-AU 1 6191746 6191746 single base substitution C T 5_prime_UTR_variant MELA-AU 1 6191746 6191746 single base substitution C T exon_variant MELA-AU 1 6191746 6191746 single base substitution C T synonymous_variant R1069R 3207G>A MELA-AU 1 6191746 6191746 single base substitution C T upstream_gene_variant MELA-AU 1 6191763 6191763 single base substitution C T 5_prime_UTR_variant MELA-AU 1 6191763 6191763 single base substitution C T exon_variant MELA-AU 1 6191763 6191763 single base substitution C T missense_variant G1064S 3190G>A MELA-AU 1 6191763 6191763 single base substitution C T upstream_gene_variant MELA-AU 1 6191956 6191957 multiple base substitution (>=2bp and <=200bp) CT TC intron_variant MELA-AU 1 6191956 6191957 multiple base substitution (>=2bp and <=200bp) CT TC upstream_gene_variant MELA-AU 1 6191977 6191977 single base substitution A C intron_variant MELA-AU 1 6191977 6191977 single base substitution A C upstream_gene_variant MELA-AU 1 6192173 6192173 single base substitution G A intron_variant MELA-AU 1 6192173 6192173 single base substitution G A upstream_gene_variant MELA-AU 1 6192238 6192238 single base substitution C T intron_variant MELA-AU 1 6192238 6192238 single base substitution C T upstream_gene_variant MELA-AU 1 6192278 6192278 single base substitution C T intron_variant MELA-AU 1 6192278 6192278 single base substitution C T upstream_gene_variant MELA-AU 1 6192368 6192368 single base substitution G A intron_variant MELA-AU 1 6192368 6192368 single base substitution G A upstream_gene_variant MELA-AU 1 6192591 6192591 single base substitution C T intron_variant MELA-AU 1 6192591 6192591 single base substitution C T upstream_gene_variant MELA-AU 1 6192795 6192795 single base substitution C T intron_variant MELA-AU 1 6192795 6192795 single base substitution C T upstream_gene_variant MELA-AU 1 6192879 6192879 single base substitution C T intron_variant MELA-AU 1 6192879 6192879 single base substitution C T upstream_gene_variant MELA-AU 1 6192973 6192973 single base substitution G A intron_variant MELA-AU 1 6192973 6192973 single base substitution G A upstream_gene_variant MELA-AU 1 6193157 6193157 single base substitution G A intron_variant MELA-AU 1 6193157 6193157 single base substitution G A upstream_gene_variant MELA-AU 1 6193195 6193195 single base substitution G A intron_variant MELA-AU 1 6193195 6193195 single base substitution G A upstream_gene_variant MELA-AU 1 6193220 6193220 single base substitution G A intron_variant MELA-AU 1 6193220 6193220 single base substitution G A upstream_gene_variant MELA-AU 1 6193276 6193276 single base substitution C T intron_variant MELA-AU 1 6193276 6193276 single base substitution C T upstream_gene_variant MELA-AU 1 6193308 6193308 single base substitution G A intron_variant MELA-AU 1 6193308 6193308 single base substitution G A upstream_gene_variant MELA-AU 1 6193425 6193425 single base substitution G A intron_variant MELA-AU 1 6193425 6193425 single base substitution G A upstream_gene_variant MELA-AU 1 6193683 6193683 single base substitution G A intron_variant MELA-AU 1 6193683 6193683 single base substitution G A upstream_gene_variant MELA-AU 1 6193775 6193775 single base substitution C T intron_variant MELA-AU 1 6193775 6193775 single base substitution C T upstream_gene_variant MELA-AU 1 6193901 6193901 single base substitution G A intron_variant MELA-AU 1 6193901 6193901 single base substitution G A upstream_gene_variant MELA-AU 1 6193981 6193981 single base substitution T C intron_variant MELA-AU 1 6193981 6193981 single base substitution T C upstream_gene_variant MELA-AU 1 6194221 6194221 single base substitution C T 5_prime_UTR_variant MELA-AU 1 6194221 6194221 single base substitution C T exon_variant MELA-AU 1 6194221 6194221 single base substitution C T synonymous_variant R1037R 3111G>A MELA-AU 1 6194221 6194221 single base substitution C T upstream_gene_variant MELA-AU 1 6194271 6194271 single base substitution T G 5_prime_UTR_variant MELA-AU 1 6194271 6194271 single base substitution T G exon_variant MELA-AU 1 6194271 6194271 single base substitution T G missense_variant K1021Q 3061A>C MELA-AU 1 6194271 6194271 single base substitution T G upstream_gene_variant MELA-AU 1 6194460 6194460 single base substitution G A intron_variant MELA-AU 1 6194460 6194460 single base substitution G A upstream_gene_variant MELA-AU 1 6194695 6194695 single base substitution G A intron_variant MELA-AU 1 6194695 6194695 single base substitution G A upstream_gene_variant MELA-AU 1 6194730 6194730 single base substitution T C intron_variant MELA-AU 1 6194730 6194730 single base substitution T C upstream_gene_variant MELA-AU 1 6194766 6194766 single base substitution G A intron_variant MELA-AU 1 6194766 6194766 single base substitution G A upstream_gene_variant MELA-AU 1 6194793 6194793 single base substitution G A 5_prime_UTR_variant MELA-AU 1 6194793 6194793 single base substitution G A exon_variant MELA-AU 1 6194793 6194793 single base substitution G A synonymous_variant F999F 2997C>T MELA-AU 1 6194793 6194793 single base substitution G A upstream_gene_variant MELA-AU 1 6194847 6194847 single base substitution C T 5_prime_UTR_variant MELA-AU 1 6194847 6194847 single base substitution C T exon_variant MELA-AU 1 6194847 6194847 single base substitution C T synonymous_variant S981S 2943G>A MELA-AU 1 6194847 6194847 single base substitution C T upstream_gene_variant MELA-AU 1 6194883 6194883 single base substitution C T 5_prime_UTR_variant MELA-AU 1 6194883 6194883 single base substitution C T exon_variant MELA-AU 1 6194883 6194883 single base substitution C T synonymous_variant E969E 2907G>A MELA-AU 1 6194883 6194883 single base substitution C T upstream_gene_variant MELA-AU 1 6195240 6195241 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 1 6195240 6195241 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 1 6195336 6195336 single base substitution C T 5_prime_UTR_variant MELA-AU 1 6195336 6195336 single base substitution C T exon_variant MELA-AU 1 6195336 6195336 single base substitution C T missense_variant A942T 2824G>A MELA-AU 1 6195336 6195336 single base substitution C T upstream_gene_variant MELA-AU 1 6195488 6195488 single base substitution G A intron_variant MELA-AU 1 6195488 6195488 single base substitution G A upstream_gene_variant MELA-AU 1 6195560 6195560 single base substitution G A intron_variant MELA-AU 1 6195560 6195560 single base substitution G A upstream_gene_variant MELA-AU 1 6195676 6195676 single base substitution C T intron_variant MELA-AU 1 6195676 6195676 single base substitution C T upstream_gene_variant MELA-AU 1 6195694 6195694 single base substitution G A intron_variant MELA-AU 1 6195694 6195694 single base substitution G A upstream_gene_variant MELA-AU 1 6195723 6195723 single base substitution G A intron_variant MELA-AU 1 6195723 6195723 single base substitution G A upstream_gene_variant MELA-AU 1 6195752 6195752 single base substitution G A intron_variant MELA-AU 1 6195752 6195752 single base substitution G A upstream_gene_variant MELA-AU 1 6195766 6195766 single base substitution G C intron_variant MELA-AU 1 6195766 6195766 single base substitution G C upstream_gene_variant MELA-AU 1 6195819 6195820 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 1 6195819 6195820 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 1 6195859 6195859 single base substitution G A intron_variant MELA-AU 1 6195859 6195859 single base substitution G A upstream_gene_variant MELA-AU 1 6196146 6196147 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 1 6196146 6196147 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 1 6196152 6196152 single base substitution C T intron_variant MELA-AU 1 6196152 6196152 single base substitution C T upstream_gene_variant MELA-AU 1 6196437 6196437 single base substitution G A intron_variant MELA-AU 1 6196437 6196437 single base substitution G A upstream_gene_variant MELA-AU 1 6196638 6196638 single base substitution G A 5_prime_UTR_variant MELA-AU 1 6196638 6196638 single base substitution G A exon_variant MELA-AU 1 6196638 6196638 single base substitution G A missense_variant L879F 2635C>T MELA-AU 1 6196638 6196638 single base substitution G A upstream_gene_variant MELA-AU 1 6196752 6196752 insertion of <=200bp - GG intron_variant MELA-AU 1 6196752 6196752 insertion of <=200bp - GG upstream_gene_variant MELA-AU 1 6196973 6196973 single base substitution G A intron_variant MELA-AU 1 6196974 6196974 single base substitution A T intron_variant MELA-AU 1 6197051 6197051 single base substitution G A intron_variant MELA-AU 1 6197357 6197357 single base substitution G A intron_variant MELA-AU 1 6197437 6197437 single base substitution G A intron_variant MELA-AU 1 6197555 6197555 single base substitution C T intron_variant MELA-AU 1 6197717 6197717 single base substitution G A intron_variant MELA-AU 1 6197774 6197774 single base substitution G A intron_variant MELA-AU 1 6197805 6197805 single base substitution G A intron_variant MELA-AU 1 6197895 6197895 single base substitution G A intron_variant MELA-AU 1 6198040 6198040 single base substitution G A intron_variant MELA-AU 1 6198127 6198127 single base substitution G A intron_variant MELA-AU 1 6198969 6198969 single base substitution C T intron_variant MELA-AU 1 6199725 6199725 single base substitution C T intron_variant MELA-AU 1 6199971 6199971 single base substitution C T intron_variant MELA-AU 1 6200026 6200026 single base substitution C T intron_variant MELA-AU 1 6200057 6200057 single base substitution G A intron_variant MELA-AU 1 6200210 6200210 single base substitution C T intron_variant MELA-AU 1 6200550 6200550 single base substitution C T intron_variant MELA-AU 1 6200788 6200788 single base substitution G A intron_variant MELA-AU 1 6200971 6200971 single base substitution G A intron_variant MELA-AU 1 6201226 6201226 single base substitution C T intron_variant MELA-AU 1 6201270 6201270 single base substitution G A intron_variant MELA-AU 1 6201280 6201280 single base substitution T C intron_variant MELA-AU 1 6201338 6201338 single base substitution C T intron_variant MELA-AU 1 6201354 6201354 single base substitution A T intron_variant MELA-AU 1 6201449 6201449 single base substitution G A intron_variant MELA-AU 1 6201654 6201654 single base substitution G A intron_variant MELA-AU 1 6201748 6201748 single base substitution G A intron_variant MELA-AU 1 6201867 6201867 single base substitution G A intron_variant MELA-AU 1 6201878 6201878 single base substitution G A intron_variant MELA-AU 1 6202198 6202198 single base substitution A T 5_prime_UTR_variant MELA-AU 1 6202198 6202198 single base substitution A T exon_variant MELA-AU 1 6202198 6202198 single base substitution A T missense_variant F809Y 2426T>A MELA-AU 1 6202278 6202278 single base substitution C T 5_prime_UTR_variant MELA-AU 1 6202278 6202278 single base substitution C T exon_variant MELA-AU 1 6202278 6202278 single base substitution C T synonymous_variant G782G 2346G>A MELA-AU 1 6202304 6202304 single base substitution C T 5_prime_UTR_variant MELA-AU 1 6202304 6202304 single base substitution C T exon_variant MELA-AU 1 6202304 6202304 single base substitution C T missense_variant D774N 2320G>A MELA-AU 1 6202347 6202347 single base substitution G A 5_prime_UTR_variant MELA-AU 1 6202347 6202347 single base substitution G A exon_variant MELA-AU 1 6202347 6202347 single base substitution G A synonymous_variant S759S 2277C>T MELA-AU 1 6202394 6202394 single base substitution G A splice_region_variant MELA-AU 1 6202599 6202599 single base substitution G A 5_prime_UTR_variant MELA-AU 1 6202599 6202599 single base substitution G A exon_variant MELA-AU 1 6202599 6202599 single base substitution G A stop_gained Q704* 2110C>T MELA-AU 1 6202910 6202910 single base substitution G A intron_variant MELA-AU 1 6203035 6203035 single base substitution T A intron_variant MELA-AU 1 6203582 6203582 single base substitution C T intron_variant MELA-AU 1 6203850 6203850 single base substitution C T intron_variant MELA-AU 1 6203995 6203995 single base substitution G A splice_region_variant MELA-AU 1 6204072 6204072 single base substitution C T intron_variant MELA-AU 1 6204242 6204242 single base substitution C T intron_variant MELA-AU 1 6204242 6204242 single base substitution C T upstream_gene_variant MELA-AU 1 6204402 6204402 single base substitution C T intron_variant MELA-AU 1 6204402 6204402 single base substitution C T upstream_gene_variant MELA-AU 1 6204504 6204504 single base substitution G A intron_variant MELA-AU 1 6204504 6204504 single base substitution G A upstream_gene_variant MELA-AU 1 6204561 6204561 single base substitution T C intron_variant MELA-AU 1 6204561 6204561 single base substitution T C upstream_gene_variant MELA-AU 1 6204642 6204642 single base substitution T G intron_variant MELA-AU 1 6204642 6204642 single base substitution T G upstream_gene_variant MELA-AU 1 6204675 6204676 multiple base substitution (>=2bp and <=200bp) CA AT intron_variant MELA-AU 1 6204675 6204676 multiple base substitution (>=2bp and <=200bp) CA AT upstream_gene_variant MELA-AU 1 6204748 6204748 single base substitution G A intron_variant MELA-AU 1 6204748 6204748 single base substitution G A upstream_gene_variant MELA-AU 1 6204828 6204828 single base substitution C T intron_variant MELA-AU 1 6204828 6204828 single base substitution C T upstream_gene_variant MELA-AU 1 6204964 6204964 single base substitution C T intron_variant MELA-AU 1 6204964 6204964 single base substitution C T upstream_gene_variant MELA-AU 1 6204997 6204997 single base substitution G A intron_variant MELA-AU 1 6204997 6204997 single base substitution G A upstream_gene_variant MELA-AU 1 6205011 6205011 single base substitution G A intron_variant MELA-AU 1 6205011 6205011 single base substitution G A upstream_gene_variant MELA-AU 1 6205037 6205038 deletion of <=200bp AG - intron_variant MELA-AU 1 6205037 6205038 deletion of <=200bp AG - upstream_gene_variant MELA-AU 1 6205130 6205130 single base substitution G A intron_variant MELA-AU 1 6205130 6205130 single base substitution G A upstream_gene_variant MELA-AU 1 6205171 6205171 single base substitution G A intron_variant MELA-AU 1 6205171 6205171 single base substitution G A upstream_gene_variant MELA-AU 1 6205187 6205187 single base substitution C T intron_variant MELA-AU 1 6205187 6205187 single base substitution C T upstream_gene_variant MELA-AU 1 6205387 6205387 single base substitution G A intron_variant MELA-AU 1 6205387 6205387 single base substitution G A upstream_gene_variant MELA-AU 1 6205781 6205781 single base substitution C T intron_variant MELA-AU 1 6205781 6205781 single base substitution C T upstream_gene_variant MELA-AU 1 6206164 6206164 single base substitution C T intron_variant MELA-AU 1 6206164 6206164 single base substitution C T upstream_gene_variant MELA-AU 1 6206355 6206355 single base substitution G A 5_prime_UTR_variant MELA-AU 1 6206355 6206355 single base substitution G A exon_variant MELA-AU 1 6206355 6206355 single base substitution G A synonymous_variant P573P 1719C>T MELA-AU 1 6206355 6206355 single base substitution G A upstream_gene_variant MELA-AU 1 6206480 6206480 single base substitution C T 5_prime_UTR_variant MELA-AU 1 6206480 6206480 single base substitution C T exon_variant MELA-AU 1 6206480 6206480 single base substitution C T missense_variant E532K 1594G>A MELA-AU 1 6206480 6206480 single base substitution C T upstream_gene_variant MELA-AU 1 6206484 6206484 single base substitution C T splice_acceptor_variant MELA-AU 1 6206484 6206484 single base substitution C T upstream_gene_variant MELA-AU 1 6206640 6206640 single base substitution G C intron_variant MELA-AU 1 6206640 6206640 single base substitution G C upstream_gene_variant MELA-AU 1 6206644 6206644 single base substitution C T intron_variant MELA-AU 1 6206644 6206644 single base substitution C T upstream_gene_variant MELA-AU 1 6206653 6206653 single base substitution C T intron_variant MELA-AU 1 6206653 6206653 single base substitution C T upstream_gene_variant MELA-AU 1 6207042 6207042 single base substitution C T intron_variant MELA-AU 1 6207042 6207042 single base substitution C T upstream_gene_variant MELA-AU 1 6207273 6207273 single base substitution G A intron_variant MELA-AU 1 6207273 6207273 single base substitution G A upstream_gene_variant MELA-AU 1 6207334 6207334 single base substitution G A intron_variant MELA-AU 1 6207334 6207334 single base substitution G A upstream_gene_variant MELA-AU 1 6207548 6207548 single base substitution G T intron_variant MELA-AU 1 6207548 6207548 single base substitution G T upstream_gene_variant MELA-AU 1 6207695 6207695 single base substitution G A intron_variant MELA-AU 1 6207695 6207695 single base substitution G A upstream_gene_variant MELA-AU 1 6207869 6207869 single base substitution C T intron_variant MELA-AU 1 6207869 6207869 single base substitution C T upstream_gene_variant MELA-AU 1 6208029 6208029 single base substitution G A intron_variant MELA-AU 1 6208029 6208029 single base substitution G A upstream_gene_variant MELA-AU 1 6208091 6208091 single base substitution G A intron_variant MELA-AU 1 6208091 6208091 single base substitution G A upstream_gene_variant MELA-AU 1 6208100 6208100 single base substitution G A intron_variant MELA-AU 1 6208100 6208100 single base substitution G A upstream_gene_variant MELA-AU 1 6208444 6208444 single base substitution G T intron_variant MELA-AU 1 6208444 6208444 single base substitution G T upstream_gene_variant MELA-AU 1 6208605 6208605 single base substitution G A intron_variant MELA-AU 1 6208605 6208605 single base substitution G A upstream_gene_variant MELA-AU 1 6208846 6208846 single base substitution C T intron_variant MELA-AU 1 6208846 6208846 single base substitution C T upstream_gene_variant MELA-AU 1 6209106 6209106 single base substitution C G 5_prime_UTR_variant MELA-AU 1 6209106 6209106 single base substitution C G exon_variant MELA-AU 1 6209106 6209106 single base substitution C G missense_variant K397N 1191G>C MELA-AU 1 6209106 6209106 single base substitution C G upstream_gene_variant MELA-AU 1 6209141 6209141 single base substitution G A splice_region_variant MELA-AU 1 6209141 6209141 single base substitution G A upstream_gene_variant MELA-AU 1 6209295 6209295 single base substitution C T intron_variant MELA-AU 1 6209510 6209510 single base substitution C T intron_variant MELA-AU 1 6209660 6209660 single base substitution A T intron_variant MELA-AU 1 6209761 6209761 single base substitution G A intron_variant MELA-AU 1 6210063 6210063 single base substitution G A intron_variant MELA-AU 1 6210083 6210083 single base substitution G A intron_variant MELA-AU 1 6210477 6210477 single base substitution G A intron_variant MELA-AU 1 6210485 6210485 single base substitution G A intron_variant MELA-AU 1 6210540 6210540 single base substitution G A intron_variant MELA-AU 1 6210549 6210549 single base substitution G A intron_variant MELA-AU 1 6210558 6210558 single base substitution A C intron_variant MELA-AU 1 6210560 6210560 single base substitution G A intron_variant MELA-AU 1 6210591 6210591 single base substitution G A intron_variant MELA-AU 1 6210629 6210629 single base substitution G A intron_variant MELA-AU 1 6210749 6210749 single base substitution G A intron_variant MELA-AU 1 6210790 6210790 single base substitution C T intron_variant MELA-AU 1 6210884 6210884 single base substitution C T intron_variant MELA-AU 1 6210913 6210913 single base substitution G A intron_variant MELA-AU 1 6210972 6210972 single base substitution G A intron_variant MELA-AU 1 6210973 6210973 single base substitution G A intron_variant MELA-AU 1 6211146 6211146 single base substitution C T 5_prime_UTR_variant MELA-AU 1 6211146 6211146 single base substitution C T exon_variant MELA-AU 1 6211146 6211146 single base substitution C T missense_variant E314K 940G>A MELA-AU 1 6211508 6211508 single base substitution C T intron_variant MELA-AU 1 6211529 6211529 single base substitution G A intron_variant MELA-AU 1 6211539 6211539 single base substitution C T intron_variant MELA-AU 1 6211552 6211552 single base substitution C T intron_variant MELA-AU 1 6211903 6211903 single base substitution G A intron_variant MELA-AU 1 6211937 6211937 single base substitution G A intron_variant MELA-AU 1 6211984 6211984 single base substitution C T intron_variant MELA-AU 1 6212296 6212296 single base substitution G A intron_variant MELA-AU 1 6212380 6212380 single base substitution G A intron_variant MELA-AU 1 6212527 6212527 single base substitution G A 5_prime_UTR_variant MELA-AU 1 6212527 6212527 single base substitution G A exon_variant MELA-AU 1 6212527 6212527 single base substitution G A missense_variant A272V 815C>T MELA-AU 1 6212822 6212822 single base substitution C T intron_variant MELA-AU 1 6212833 6212833 single base substitution C T intron_variant MELA-AU 1 6212890 6212890 single base substitution C T intron_variant MELA-AU 1 6212978 6212978 single base substitution C T intron_variant MELA-AU 1 6212991 6212991 single base substitution C T intron_variant MELA-AU 1 6212995 6212995 single base substitution G A intron_variant MELA-AU 1 6213139 6213139 single base substitution G A intron_variant MELA-AU 1 6213159 6213159 single base substitution G A intron_variant MELA-AU 1 6213162 6213162 single base substitution G A intron_variant MELA-AU 1 6213304 6213304 single base substitution C T intron_variant MELA-AU 1 6213417 6213417 single base substitution G T intron_variant MELA-AU 1 6213545 6213545 single base substitution C T intron_variant MELA-AU 1 6213624 6213624 single base substitution C T intron_variant MELA-AU 1 6214026 6214026 single base substitution G T intron_variant MELA-AU 1 6214145 6214145 single base substitution G A intron_variant MELA-AU 1 6214300 6214300 single base substitution C T intron_variant MELA-AU 1 6214416 6214416 single base substitution C T intron_variant MELA-AU 1 6214464 6214464 single base substitution C T intron_variant MELA-AU 1 6214673 6214673 single base substitution G A intron_variant MELA-AU 1 6214689 6214689 single base substitution G A intron_variant MELA-AU 1 6215064 6215064 single base substitution G A intron_variant MELA-AU 1 6215122 6215122 single base substitution C T intron_variant MELA-AU 1 6215262 6215262 single base substitution C T intron_variant MELA-AU 1 6215524 6215524 single base substitution C T intron_variant MELA-AU 1 6215664 6215664 single base substitution G A 5_prime_UTR_variant MELA-AU 1 6215664 6215664 single base substitution G A exon_variant MELA-AU 1 6215664 6215664 single base substitution G A synonymous_variant F167F 501C>T MELA-AU 1 6215767 6215767 single base substitution G A 5_prime_UTR_variant MELA-AU 1 6215767 6215767 single base substitution G A exon_variant MELA-AU 1 6215767 6215767 single base substitution G A missense_variant S133F 398C>T MELA-AU 1 6215999 6215999 single base substitution G A intron_variant MELA-AU 1 6216047 6216047 single base substitution G C intron_variant MELA-AU 1 6216205 6216205 single base substitution G A intron_variant MELA-AU 1 6216627 6216627 single base substitution C T intron_variant MELA-AU 1 6216632 6216632 single base substitution C T intron_variant MELA-AU 1 6216635 6216635 single base substitution G A intron_variant MELA-AU 1 6216698 6216698 single base substitution G A intron_variant MELA-AU 1 6216883 6216883 single base substitution G A intron_variant MELA-AU 1 6217040 6217040 single base substitution G A intron_variant MELA-AU 1 6217043 6217043 single base substitution T C intron_variant MELA-AU 1 6217193 6217193 single base substitution C T intron_variant MELA-AU 1 6217356 6217356 single base substitution C T intron_variant MELA-AU 1 6217421 6217421 single base substitution C T intron_variant MELA-AU 1 6217755 6217755 single base substitution C T intron_variant MELA-AU 1 6217963 6217963 single base substitution C T intron_variant MELA-AU 1 6217996 6217996 single base substitution C T intron_variant MELA-AU 1 6218159 6218159 single base substitution C T intron_variant MELA-AU 1 6218735 6218735 single base substitution C T intron_variant MELA-AU 1 6219177 6219177 single base substitution C T intron_variant MELA-AU 1 6219202 6219202 single base substitution G A intron_variant MELA-AU 1 6219372 6219372 single base substitution C T intron_variant MELA-AU 1 6219451 6219451 single base substitution G A 5_prime_UTR_variant MELA-AU 1 6219451 6219451 single base substitution G A exon_variant MELA-AU 1 6219451 6219451 single base substitution G A missense_variant A111V 332C>T MELA-AU 1 6219574 6219574 single base substitution C T missense_variant G70E 209G>A MELA-AU 1 6219574 6219574 single base substitution C T splice_region_variant MELA-AU 1 6219907 6219907 single base substitution G A intron_variant MELA-AU 1 6219976 6219976 single base substitution T G intron_variant MELA-AU 1 6219984 6219984 single base substitution G A intron_variant MELA-AU 1 6219984 6219985 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 1 6220768 6220768 single base substitution C T intron_variant MELA-AU 1 6220886 6220886 single base substitution G A intron_variant MELA-AU 1 6220887 6220887 single base substitution C T intron_variant MELA-AU 1 6220996 6220996 single base substitution C T intron_variant MELA-AU 1 6221025 6221025 single base substitution G A intron_variant MELA-AU 1 6221162 6221162 single base substitution G A intron_variant MELA-AU 1 6221219 6221219 single base substitution G A intron_variant MELA-AU 1 6221223 6221223 single base substitution G A intron_variant MELA-AU 1 6221382 6221382 single base substitution G T intron_variant MELA-AU 1 6221670 6221670 single base substitution G A intron_variant MELA-AU 1 6221898 6221898 single base substitution G A intron_variant MELA-AU 1 6221976 6221976 single base substitution G A intron_variant MELA-AU 1 6222139 6222139 single base substitution G A intron_variant MELA-AU 1 6222233 6222233 single base substitution G A intron_variant MELA-AU 1 6222233 6222234 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 1 6222372 6222372 single base substitution G A intron_variant MELA-AU 1 6222579 6222579 single base substitution C T intron_variant MELA-AU 1 6222645 6222645 single base substitution G A intron_variant MELA-AU 1 6223026 6223027 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 1 6223076 6223076 single base substitution G A intron_variant MELA-AU 1 6223167 6223167 single base substitution G A intron_variant MELA-AU 1 6223441 6223441 single base substitution G A intron_variant MELA-AU 1 6223453 6223453 single base substitution G A intron_variant MELA-AU 1 6223492 6223492 single base substitution C T intron_variant MELA-AU 1 6223962 6223962 single base substitution G A intron_variant MELA-AU 1 6224147 6224147 single base substitution G A intron_variant MELA-AU 1 6224233 6224233 single base substitution C T intron_variant MELA-AU 1 6224280 6224280 single base substitution G A intron_variant MELA-AU 1 6224300 6224300 single base substitution G A intron_variant MELA-AU 1 6224303 6224303 single base substitution G A intron_variant MELA-AU 1 6224382 6224382 single base substitution C T intron_variant MELA-AU 1 6224696 6224696 single base substitution C T intron_variant MELA-AU 1 6224744 6224744 single base substitution C T intron_variant MELA-AU 1 6224819 6224819 single base substitution G A intron_variant MELA-AU 1 6224836 6224836 single base substitution G A intron_variant MELA-AU 1 6224906 6224906 single base substitution G A intron_variant MELA-AU 1 6224981 6224981 single base substitution G A intron_variant MELA-AU 1 6225573 6225573 single base substitution G A intron_variant MELA-AU 1 6225611 6225611 single base substitution C T intron_variant MELA-AU 1 6225613 6225613 single base substitution G A intron_variant MELA-AU 1 6225702 6225702 single base substitution C T intron_variant MELA-AU 1 6225760 6225760 single base substitution C T intron_variant MELA-AU 1 6225818 6225818 single base substitution G A intron_variant MELA-AU 1 6225819 6225819 single base substitution G A intron_variant MELA-AU 1 6225837 6225837 single base substitution C T intron_variant MELA-AU 1 6225842 6225843 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 1 6225863 6225863 single base substitution C T intron_variant MELA-AU 1 6225870 6225870 single base substitution G A intron_variant MELA-AU 1 6225943 6225943 single base substitution G A intron_variant MELA-AU 1 6225959 6225959 single base substitution T C intron_variant MELA-AU 1 6225966 6225966 single base substitution C T intron_variant MELA-AU 1 6226628 6226628 single base substitution C T intron_variant MELA-AU 1 6226694 6226694 single base substitution G A intron_variant MELA-AU 1 6226790 6226790 single base substitution G A intron_variant MELA-AU 1 6226808 6226808 single base substitution G A intron_variant MELA-AU 1 6226836 6226836 single base substitution C T intron_variant MELA-AU 1 6227008 6227008 single base substitution C T intron_variant MELA-AU 1 6227392 6227392 single base substitution C T intron_variant MELA-AU 1 6227522 6227522 single base substitution G A intron_variant MELA-AU 1 6227717 6227717 single base substitution G A intron_variant MELA-AU 1 6227767 6227767 single base substitution G A intron_variant MELA-AU 1 6227780 6227780 single base substitution G A intron_variant MELA-AU 1 6227869 6227869 single base substitution G A intron_variant MELA-AU 1 6227943 6227943 single base substitution C T intron_variant MELA-AU 1 6227974 6227974 single base substitution G A intron_variant MELA-AU 1 6228185 6228185 single base substitution C T intron_variant MELA-AU 1 6228275 6228275 single base substitution G A 5_prime_UTR_variant MELA-AU 1 6228275 6228275 single base substitution G A exon_variant MELA-AU 1 6228275 6228275 single base substitution G A missense_variant P48S 142C>T MELA-AU 1 6228971 6228971 single base substitution C T intron_variant MELA-AU 1 6228993 6228993 single base substitution C T intron_variant MELA-AU 1 6229050 6229050 single base substitution G A intron_variant MELA-AU 1 6229054 6229054 single base substitution G A intron_variant MELA-AU 1 6229057 6229057 single base substitution C T intron_variant MELA-AU 1 6229666 6229666 single base substitution G A intron_variant MELA-AU 1 6229769 6229769 single base substitution G A intron_variant MELA-AU 1 6229770 6229770 single base substitution G A intron_variant MELA-AU 1 6229936 6229936 single base substitution T A intron_variant MELA-AU 1 6230041 6230042 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 1 6230094 6230094 single base substitution G A intron_variant MELA-AU 1 6230139 6230140 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 1 6230264 6230264 single base substitution G A intron_variant MELA-AU 1 6230495 6230495 single base substitution G T intron_variant MELA-AU 1 6230497 6230497 single base substitution G A intron_variant MELA-AU 1 6230741 6230741 single base substitution G A intron_variant MELA-AU 1 6230829 6230829 single base substitution G A intron_variant MELA-AU 1 6230834 6230834 single base substitution T G intron_variant MELA-AU 1 6231094 6231094 single base substitution G A intron_variant MELA-AU 1 6231133 6231133 single base substitution C T intron_variant MELA-AU 1 6231157 6231157 single base substitution G A intron_variant MELA-AU 1 6231332 6231332 single base substitution G A intron_variant MELA-AU 1 6231344 6231344 single base substitution C T intron_variant MELA-AU 1 6231600 6231600 single base substitution A C intron_variant MELA-AU 1 6231672 6231672 single base substitution A T intron_variant MELA-AU 1 6231783 6231783 single base substitution G A intron_variant MELA-AU 1 6231869 6231869 single base substitution G A intron_variant MELA-AU 1 6232068 6232068 single base substitution G A intron_variant MELA-AU 1 6232236 6232236 single base substitution C T intron_variant MELA-AU 1 6232476 6232476 single base substitution C T intron_variant MELA-AU 1 6232508 6232508 single base substitution C T intron_variant MELA-AU 1 6232557 6232557 single base substitution C T intron_variant MELA-AU 1 6232584 6232584 single base substitution G A intron_variant MELA-AU 1 6232819 6232819 single base substitution G A intron_variant MELA-AU 1 6233547 6233547 single base substitution G A intron_variant MELA-AU 1 6233630 6233630 single base substitution C T intron_variant MELA-AU 1 6233677 6233677 single base substitution G A intron_variant MELA-AU 1 6234097 6234097 single base substitution G A intron_variant MELA-AU 1 6234100 6234100 single base substitution G A intron_variant MELA-AU 1 6234152 6234152 single base substitution G A intron_variant MELA-AU 1 6234239 6234239 single base substitution G A intron_variant MELA-AU 1 6234287 6234287 single base substitution G A intron_variant MELA-AU 1 6234292 6234292 single base substitution G A intron_variant MELA-AU 1 6234296 6234296 single base substitution G A intron_variant MELA-AU 1 6234587 6234587 single base substitution G A intron_variant MELA-AU 1 6234670 6234670 single base substitution G A intron_variant MELA-AU 1 6234868 6234868 single base substitution G A intron_variant MELA-AU 1 6234882 6234882 single base substitution G A intron_variant MELA-AU 1 6235053 6235053 single base substitution G A intron_variant MELA-AU 1 6235217 6235217 single base substitution G A intron_variant MELA-AU 1 6235257 6235257 single base substitution G A intron_variant MELA-AU 1 6235322 6235322 single base substitution G A intron_variant MELA-AU 1 6235389 6235389 single base substitution G C intron_variant MELA-AU 1 6235453 6235453 single base substitution G A intron_variant MELA-AU 1 6235583 6235583 single base substitution G A intron_variant MELA-AU 1 6235886 6235886 single base substitution G A intron_variant MELA-AU 1 6236218 6236218 single base substitution G A intron_variant MELA-AU 1 6236311 6236311 single base substitution G A intron_variant MELA-AU 1 6236614 6236614 single base substitution C T intron_variant MELA-AU 1 6236628 6236628 single base substitution G A intron_variant MELA-AU 1 6236845 6236846 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 1 6237131 6237131 single base substitution C T intron_variant MELA-AU 1 6237357 6237357 single base substitution G A intron_variant MELA-AU 1 6237568 6237568 single base substitution C T intron_variant MELA-AU 1 6238074 6238074 single base substitution G A intron_variant MELA-AU 1 6238234 6238234 single base substitution G A intron_variant MELA-AU 1 6238307 6238307 single base substitution A T intron_variant MELA-AU 1 6238972 6238972 single base substitution G A intron_variant MELA-AU 1 6240116 6240116 single base substitution C T 5_prime_UTR_variant MELA-AU 1 6240116 6240116 single base substitution C T upstream_gene_variant MELA-AU 1 6242398 6242398 single base substitution G A upstream_gene_variant MELA-AU 1 6242824 6242824 single base substitution C A upstream_gene_variant MELA-AU 1 6243103 6243103 single base substitution G A upstream_gene_variant MELA-AU 1 6243476 6243476 single base substitution C T upstream_gene_variant MELA-AU 1 6244316 6244316 deletion of <=200bp C - upstream_gene_variant MELA-AU 1 6244460 6244460 single base substitution G A upstream_gene_variant MELA-AU 1 6244680 6244680 single base substitution G A upstream_gene_variant MELA-AU 1 6244947 6244947 single base substitution G A upstream_gene_variant ORCA-IN 1 6182331 6182331 single base substitution C T downstream_gene_variant ORCA-IN 1 6182331 6182331 single base substitution C T intron_variant ORCA-IN 1 6188110 6188110 single base substitution C A 3_prime_UTR_variant ORCA-IN 1 6188110 6188110 single base substitution C A exon_variant ORCA-IN 1 6188110 6188110 single base substitution C A intron_variant ORCA-IN 1 6188110 6188110 single base substitution C A missense_variant G1300V 3899G>T ORCA-IN 1 6188110 6188110 single base substitution C A missense_variant G157V 470G>T ORCA-IN 1 6191704 6191704 single base substitution G T 5_prime_UTR_variant ORCA-IN 1 6191704 6191704 single base substitution G T exon_variant ORCA-IN 1 6191704 6191704 single base substitution G T synonymous_variant I1083I 3249C>A ORCA-IN 1 6191704 6191704 single base substitution G T upstream_gene_variant ORCA-IN 1 6192281 6192281 single base substitution C T intron_variant ORCA-IN 1 6192281 6192281 single base substitution C T upstream_gene_variant ORCA-IN 1 6194889 6194889 single base substitution G T 5_prime_UTR_variant ORCA-IN 1 6194889 6194889 single base substitution G T exon_variant ORCA-IN 1 6194889 6194889 single base substitution G T missense_variant N967K 2901C>A ORCA-IN 1 6194889 6194889 single base substitution G T upstream_gene_variant ORCA-IN 1 6202394 6202394 single base substitution G A splice_region_variant ORCA-IN 1 6209079 6209079 single base substitution G T 5_prime_UTR_variant ORCA-IN 1 6209079 6209079 single base substitution G T exon_variant ORCA-IN 1 6209079 6209079 single base substitution G T synonymous_variant G406G 1218C>A ORCA-IN 1 6209079 6209079 single base substitution G T upstream_gene_variant ORCA-IN 1 6210269 6210269 single base substitution A G intron_variant ORCA-IN 1 6211756 6211756 single base substitution G A intron_variant ORCA-IN 1 6234175 6234175 single base substitution G A intron_variant ORCA-IN 1 6237063 6237063 single base substitution G A intron_variant ORCA-IN 1 6242768 6242768 single base substitution G A upstream_gene_variant OV-AU 1 6164351 6164351 single base substitution G C 3_prime_UTR_variant OV-AU 1 6164351 6164351 single base substitution G C downstream_gene_variant OV-AU 1 6165439 6165439 single base substitution G A 3_prime_UTR_variant OV-AU 1 6165439 6165439 single base substitution G A missense_variant P806S 2416C>T OV-AU 1 6165439 6165439 single base substitution G A missense_variant P87S 259C>T OV-AU 1 6165785 6165785 single base substitution C A intron_variant OV-AU 1 6167462 6167462 single base substitution T G intron_variant OV-AU 1 6167462 6167462 single base substitution T G upstream_gene_variant OV-AU 1 6167990 6167990 single base substitution G A intron_variant OV-AU 1 6167990 6167990 single base substitution G A upstream_gene_variant OV-AU 1 6168462 6168462 single base substitution G A intron_variant OV-AU 1 6168462 6168462 single base substitution G A upstream_gene_variant OV-AU 1 6177602 6177602 single base substitution T A intron_variant OV-AU 1 6179751 6179751 single base substitution T A intron_variant OV-AU 1 6185676 6185676 single base substitution G C intron_variant OV-AU 1 6185676 6185676 single base substitution G C splice_region_variant OV-AU 1 6186284 6186284 single base substitution G A intron_variant OV-AU 1 6186356 6186356 single base substitution A C intron_variant OV-AU 1 6190423 6190423 single base substitution G T intron_variant OV-AU 1 6190423 6190423 single base substitution G T upstream_gene_variant OV-AU 1 6194491 6194491 single base substitution A G intron_variant OV-AU 1 6194491 6194491 single base substitution A G upstream_gene_variant OV-AU 1 6196165 6196165 single base substitution T C intron_variant OV-AU 1 6196165 6196165 single base substitution T C upstream_gene_variant OV-AU 1 6209676 6209676 single base substitution A G intron_variant OV-AU 1 6210606 6210606 single base substitution G A intron_variant OV-AU 1 6214378 6214378 single base substitution T A intron_variant OV-AU 1 6216022 6216022 single base substitution G A intron_variant OV-AU 1 6219236 6219236 single base substitution G A intron_variant OV-AU 1 6225909 6225909 single base substitution C G intron_variant OV-AU 1 6234134 6234134 single base substitution G T intron_variant OV-AU 1 6234740 6234740 single base substitution A T intron_variant OV-AU 1 6242364 6242364 single base substitution G A upstream_gene_variant OV-US 1 6206923 6206923 insertion of <=200bp - G 5_prime_UTR_variant OV-US 1 6206923 6206923 insertion of <=200bp - G exon_variant OV-US 1 6206923 6206923 insertion of <=200bp - G frameshift_variant P464P? OV-US 1 6206923 6206923 insertion of <=200bp - G upstream_gene_variant PACA-AU 1 6157699 6157699 single base substitution G A downstream_gene_variant PACA-AU 1 6159408 6159408 single base substitution C T downstream_gene_variant PACA-AU 1 6166094 6166094 single base substitution G A intron_variant PACA-AU 1 6168629 6168629 single base substitution G C intron_variant PACA-AU 1 6168629 6168629 single base substitution G C upstream_gene_variant PACA-AU 1 6168965 6168965 single base substitution G A intron_variant PACA-AU 1 6168965 6168965 single base substitution G A upstream_gene_variant PACA-AU 1 6170517 6170517 single base substitution C T 3_prime_UTR_variant PACA-AU 1 6170517 6170517 single base substitution C T synonymous_variant K1773K 5319G>A PACA-AU 1 6170517 6170517 single base substitution C T synonymous_variant K630K 1890G>A PACA-AU 1 6170517 6170517 single base substitution C T upstream_gene_variant PACA-AU 1 6172210 6172210 single base substitution C G 3_prime_UTR_variant PACA-AU 1 6172210 6172210 single base substitution C G synonymous_variant G1710G 5130G>C PACA-AU 1 6172210 6172210 single base substitution C G synonymous_variant G567G 1701G>C PACA-AU 1 6173327 6173329 deletion of <=200bp ACA - intron_variant PACA-AU 1 6179349 6179349 single base substitution C T intron_variant PACA-AU 1 6181216 6181216 single base substitution G A 3_prime_UTR_variant PACA-AU 1 6181216 6181216 single base substitution G A downstream_gene_variant PACA-AU 1 6181216 6181216 single base substitution G A exon_variant PACA-AU 1 6181216 6181216 single base substitution G A missense_variant R1621W 4861C>T PACA-AU 1 6181216 6181216 single base substitution G A missense_variant R478W 1432C>T PACA-AU 1 6182583 6182583 single base substitution G A downstream_gene_variant PACA-AU 1 6182583 6182583 single base substitution G A intron_variant PACA-AU 1 6183457 6183457 single base substitution A C downstream_gene_variant PACA-AU 1 6183457 6183457 single base substitution A C intron_variant PACA-AU 1 6185737 6185737 single base substitution C T intron_variant PACA-AU 1 6195280 6195280 single base substitution C T intron_variant PACA-AU 1 6195280 6195280 single base substitution C T upstream_gene_variant PACA-AU 1 6195295 6195295 single base substitution C T 5_prime_UTR_variant PACA-AU 1 6195295 6195295 single base substitution C T exon_variant PACA-AU 1 6195295 6195295 single base substitution C T missense_variant M955I 2865G>A PACA-AU 1 6195295 6195295 single base substitution C T upstream_gene_variant PACA-AU 1 6195356 6195356 single base substitution T C 5_prime_UTR_variant PACA-AU 1 6195356 6195356 single base substitution T C exon_variant PACA-AU 1 6195356 6195356 single base substitution T C missense_variant D935G 2804A>G PACA-AU 1 6195356 6195356 single base substitution T C upstream_gene_variant PACA-AU 1 6200174 6200174 single base substitution A G intron_variant PACA-AU 1 6210730 6210730 single base substitution G C intron_variant PACA-AU 1 6219363 6219363 single base substitution G A intron_variant PACA-AU 1 6224309 6224309 single base substitution G A intron_variant PACA-AU 1 6225186 6225186 single base substitution G A intron_variant PACA-AU 1 6225212 6225212 single base substitution G A intron_variant PACA-AU 1 6226767 6226767 single base substitution C T intron_variant PACA-AU 1 6228354 6228354 single base substitution G A intron_variant PACA-AU 1 6230204 6230204 single base substitution A C intron_variant PACA-AU 1 6230246 6230246 single base substitution C T intron_variant PACA-AU 1 6231158 6231158 single base substitution A G intron_variant PACA-AU 1 6232851 6232851 single base substitution C T intron_variant PACA-AU 1 6235343 6235343 single base substitution G C intron_variant PACA-AU 1 6237435 6237435 single base substitution C T intron_variant PACA-AU 1 6237569 6237569 single base substitution G A intron_variant PACA-AU 1 6242229 6242229 single base substitution C T upstream_gene_variant PACA-AU 1 6243029 6243029 single base substitution T G upstream_gene_variant PACA-CA 1 6156915 6156915 single base substitution G C downstream_gene_variant PACA-CA 1 6158667 6158667 single base substitution G A downstream_gene_variant PACA-CA 1 6158691 6158691 single base substitution C T downstream_gene_variant PACA-CA 1 6161051 6161051 single base substitution G C downstream_gene_variant PACA-CA 1 6161464 6161464 single base substitution C T downstream_gene_variant PACA-CA 1 6163065 6163065 single base substitution G A 3_prime_UTR_variant PACA-CA 1 6163065 6163065 single base substitution G A downstream_gene_variant PACA-CA 1 6163638 6163638 single base substitution T C 3_prime_UTR_variant PACA-CA 1 6163638 6163638 single base substitution T C downstream_gene_variant PACA-CA 1 6164064 6164064 single base substitution C A 3_prime_UTR_variant PACA-CA 1 6164064 6164064 single base substitution C A downstream_gene_variant PACA-CA 1 6167112 6167112 single base substitution A G intron_variant PACA-CA 1 6167112 6167112 single base substitution A G upstream_gene_variant PACA-CA 1 6167835 6167835 deletion of <=200bp G - intron_variant PACA-CA 1 6167835 6167835 deletion of <=200bp G - upstream_gene_variant PACA-CA 1 6172391 6172391 single base substitution G C intron_variant PACA-CA 1 6174816 6174816 insertion of <=200bp - A intron_variant PACA-CA 1 6177014 6177014 single base substitution C A intron_variant PACA-CA 1 6178993 6178993 single base substitution G T intron_variant PACA-CA 1 6179074 6179074 single base substitution A C intron_variant PACA-CA 1 6179811 6179811 single base substitution G A intron_variant PACA-CA 1 6181895 6181895 single base substitution G T downstream_gene_variant PACA-CA 1 6181895 6181895 single base substitution G T intron_variant PACA-CA 1 6182088 6182088 single base substitution G A downstream_gene_variant PACA-CA 1 6182088 6182088 single base substitution G A intron_variant PACA-CA 1 6183302 6183302 single base substitution A G downstream_gene_variant PACA-CA 1 6183302 6183302 single base substitution A G intron_variant PACA-CA 1 6183676 6183676 single base substitution C T downstream_gene_variant PACA-CA 1 6183676 6183676 single base substitution C T intron_variant PACA-CA 1 6192368 6192368 single base substitution G C intron_variant PACA-CA 1 6192368 6192368 single base substitution G C upstream_gene_variant PACA-CA 1 6193467 6193467 single base substitution G A intron_variant PACA-CA 1 6193467 6193467 single base substitution G A upstream_gene_variant PACA-CA 1 6194165 6194165 single base substitution G A intron_variant PACA-CA 1 6194165 6194165 single base substitution G A upstream_gene_variant PACA-CA 1 6195228 6195228 single base substitution C G intron_variant PACA-CA 1 6195228 6195228 single base substitution C G upstream_gene_variant PACA-CA 1 6195253 6195253 single base substitution C T intron_variant PACA-CA 1 6195253 6195253 single base substitution C T upstream_gene_variant PACA-CA 1 6195315 6195315 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant PACA-CA 1 6195315 6195315 single base substitution G A exon_variant PACA-CA 1 6195315 6195315 single base substitution G A missense_variant R949W 2845C>T PACA-CA 1 6195315 6195315 single base substitution G A upstream_gene_variant PACA-CA 1 6197120 6197120 single base substitution C T intron_variant PACA-CA 1 6198216 6198216 single base substitution A G intron_variant PACA-CA 1 6205258 6205258 single base substitution G A intron_variant PACA-CA 1 6205258 6205258 single base substitution G A upstream_gene_variant PACA-CA 1 6206100 6206100 single base substitution C T intron_variant PACA-CA 1 6206100 6206100 single base substitution C T upstream_gene_variant PACA-CA 1 6210523 6210523 single base substitution T C intron_variant PACA-CA 1 6212784 6212784 single base substitution A T intron_variant PACA-CA 1 6214446 6214446 single base substitution G A intron_variant PACA-CA 1 6215610 6215610 single base substitution C T intron_variant PACA-CA 1 6216659 6216659 single base substitution C T intron_variant PACA-CA 1 6217922 6217922 single base substitution C G intron_variant PACA-CA 1 6220320 6220320 single base substitution C A intron_variant PACA-CA 1 6220928 6220928 single base substitution C T intron_variant PACA-CA 1 6225985 6225985 single base substitution C T intron_variant PACA-CA 1 6229093 6229093 single base substitution A G intron_variant PACA-CA 1 6230260 6230260 single base substitution G T intron_variant PACA-CA 1 6231588 6231588 single base substitution G A intron_variant PACA-CA 1 6235501 6235501 single base substitution A T intron_variant PACA-CA 1 6237003 6237003 single base substitution G A intron_variant PACA-CA 1 6238318 6238318 single base substitution G C intron_variant PACA-CA 1 6238765 6238765 single base substitution T C intron_variant PACA-CA 1 6240917 6240917 single base substitution G A upstream_gene_variant PACA-CA 1 6242697 6242697 insertion of <=200bp - G upstream_gene_variant PACA-CA 1 6242853 6242853 single base substitution C G upstream_gene_variant PAEN-AU 1 6157329 6157329 single base substitution C T downstream_gene_variant PAEN-AU 1 6181697 6181697 single base substitution T G downstream_gene_variant PAEN-AU 1 6181697 6181697 single base substitution T G intron_variant PAEN-AU 1 6229021 6229021 single base substitution G A intron_variant PAEN-AU 1 6235343 6235343 single base substitution G C intron_variant PAEN-AU 1 6243321 6243321 single base substitution C G upstream_gene_variant PAEN-IT 1 6162060 6162060 single base substitution C T 3_prime_UTR_variant PAEN-IT 1 6162060 6162060 single base substitution C T downstream_gene_variant PAEN-IT 1 6171894 6171894 single base substitution C A 3_prime_UTR_variant PAEN-IT 1 6171894 6171894 single base substitution C A synonymous_variant G1730G 5190G>T PAEN-IT 1 6171894 6171894 single base substitution C A synonymous_variant G587G 1761G>T PBCA-DE 1 6156996 6156996 single base substitution C T downstream_gene_variant PBCA-DE 1 6162251 6162252 deletion of <=200bp AC - 3_prime_UTR_variant PBCA-DE 1 6162251 6162252 deletion of <=200bp AC - downstream_gene_variant PBCA-DE 1 6163830 6163830 single base substitution C T 3_prime_UTR_variant PBCA-DE 1 6163830 6163830 single base substitution C T downstream_gene_variant PBCA-DE 1 6167602 6167602 single base substitution G T intron_variant PBCA-DE 1 6167602 6167602 single base substitution G T upstream_gene_variant PBCA-DE 1 6167677 6167677 single base substitution A G intron_variant PBCA-DE 1 6167677 6167677 single base substitution A G upstream_gene_variant PBCA-DE 1 6167678 6167678 single base substitution T G intron_variant PBCA-DE 1 6167678 6167678 single base substitution T G upstream_gene_variant PBCA-DE 1 6167682 6167682 insertion of <=200bp - GAT intron_variant PBCA-DE 1 6167682 6167682 insertion of <=200bp - GAT upstream_gene_variant PBCA-DE 1 6170836 6170836 single base substitution C T intron_variant PBCA-DE 1 6170836 6170836 single base substitution C T upstream_gene_variant PBCA-DE 1 6174137 6174137 single base substitution G A intron_variant PBCA-DE 1 6176301 6176302 deletion of <=200bp AT - intron_variant PBCA-DE 1 6179053 6179053 single base substitution C T intron_variant PBCA-DE 1 6182434 6182434 single base substitution T C downstream_gene_variant PBCA-DE 1 6182434 6182434 single base substitution T C intron_variant PBCA-DE 1 6184763 6184763 single base substitution C G downstream_gene_variant PBCA-DE 1 6184763 6184763 single base substitution C G intron_variant PBCA-DE 1 6187305 6187305 single base substitution G A intron_variant PBCA-DE 1 6193546 6193546 single base substitution G T intron_variant PBCA-DE 1 6193546 6193546 single base substitution G T upstream_gene_variant PBCA-DE 1 6194018 6194018 single base substitution C T intron_variant PBCA-DE 1 6194018 6194018 single base substitution C T upstream_gene_variant PBCA-DE 1 6194747 6194747 single base substitution A G intron_variant PBCA-DE 1 6194747 6194747 single base substitution A G upstream_gene_variant PBCA-DE 1 6205344 6205344 single base substitution T G intron_variant PBCA-DE 1 6205344 6205344 single base substitution T G upstream_gene_variant PBCA-DE 1 6219000 6219000 single base substitution A G intron_variant PBCA-DE 1 6219288 6219289 deletion of <=200bp CA - intron_variant PBCA-DE 1 6225279 6225279 single base substitution C A intron_variant PBCA-DE 1 6228175 6228175 single base substitution G A intron_variant PBCA-DE 1 6232693 6232693 single base substitution G A intron_variant PBCA-DE 1 6234107 6234107 single base substitution C T intron_variant PBCA-DE 1 6238399 6238399 single base substitution G A intron_variant PRAD-CA 1 6160965 6160965 single base substitution G A downstream_gene_variant PRAD-CA 1 6167602 6167602 single base substitution G T intron_variant PRAD-CA 1 6167602 6167602 single base substitution G T upstream_gene_variant PRAD-CA 1 6168376 6168376 single base substitution C T intron_variant PRAD-CA 1 6168376 6168376 single base substitution C T upstream_gene_variant PRAD-CA 1 6189013 6189013 single base substitution G C 3_prime_UTR_variant PRAD-CA 1 6189013 6189013 single base substitution G C exon_variant PRAD-CA 1 6189013 6189013 single base substitution G C intron_variant PRAD-CA 1 6189013 6189013 single base substitution G C synonymous_variant L1168L 3504C>G PRAD-CA 1 6189013 6189013 single base substitution G C synonymous_variant L25L 75C>G PRAD-CA 1 6189013 6189013 single base substitution G C upstream_gene_variant PRAD-CA 1 6196739 6196739 single base substitution G A intron_variant PRAD-CA 1 6196739 6196739 single base substitution G A upstream_gene_variant PRAD-CA 1 6218146 6218146 single base substitution G T intron_variant PRAD-CA 1 6230361 6230361 single base substitution C T intron_variant PRAD-UK 1 6161303 6161303 single base substitution C T downstream_gene_variant PRAD-UK 1 6180168 6180168 single base substitution G A intron_variant PRAD-UK 1 6191350 6191350 single base substitution G A intron_variant PRAD-UK 1 6191350 6191350 single base substitution G A upstream_gene_variant PRAD-UK 1 6200073 6200073 single base substitution G A intron_variant PRAD-UK 1 6202156 6202156 single base substitution C T intron_variant PRAD-UK 1 6204834 6204834 deletion of <=200bp G - intron_variant PRAD-UK 1 6204834 6204834 deletion of <=200bp G - upstream_gene_variant PRAD-UK 1 6206903 6206903 single base substitution C T 5_prime_UTR_variant PRAD-UK 1 6206903 6206903 single base substitution C T exon_variant PRAD-UK 1 6206903 6206903 single base substitution C T missense_variant R471Q 1412G>A PRAD-UK 1 6206903 6206903 single base substitution C T upstream_gene_variant PRAD-UK 1 6211807 6211807 insertion of <=200bp - AC intron_variant PRAD-UK 1 6211811 6211811 insertion of <=200bp - AC intron_variant PRAD-UK 1 6225014 6225014 single base substitution C T intron_variant PRAD-UK 1 6237808 6237808 deletion of <=200bp A - intron_variant PRAD-UK 1 6243271 6243271 single base substitution G C upstream_gene_variant PRAD-US 1 6166702 6166702 single base substitution G A 3_prime_UTR_variant PRAD-US 1 6166702 6166702 single base substitution G A missense_variant R1906C 5716C>T PRAD-US 1 6166702 6166702 single base substitution G A missense_variant R44C 130C>T PRAD-US 1 6166702 6166702 single base substitution G A missense_variant R763C 2287C>T PRAD-US 1 6181216 6181216 single base substitution G A 3_prime_UTR_variant PRAD-US 1 6181216 6181216 single base substitution G A downstream_gene_variant PRAD-US 1 6181216 6181216 single base substitution G A exon_variant PRAD-US 1 6181216 6181216 single base substitution G A missense_variant R1621W 4861C>T PRAD-US 1 6181216 6181216 single base substitution G A missense_variant R478W 1432C>T PRAD-US 1 6228311 6228311 single base substitution A T 5_prime_UTR_variant PRAD-US 1 6228311 6228311 single base substitution A T exon_variant PRAD-US 1 6228311 6228311 single base substitution A T missense_variant F36I 106T>A READ-US 1 6158553 6158553 single base substitution G A downstream_gene_variant READ-US 1 6172270 6172270 single base substitution G A 3_prime_UTR_variant READ-US 1 6172270 6172270 single base substitution G A synonymous_variant D1690D 5070C>T READ-US 1 6172270 6172270 single base substitution G A synonymous_variant D547D 1641C>T READ-US 1 6172981 6172981 single base substitution C T 3_prime_UTR_variant READ-US 1 6172981 6172981 single base substitution C T missense_variant E1664K 4990G>A READ-US 1 6172981 6172981 single base substitution C T missense_variant E521K 1561G>A READ-US 1 6228223 6228223 single base substitution C T 5_prime_UTR_variant READ-US 1 6228223 6228223 single base substitution C T exon_variant READ-US 1 6228223 6228223 single base substitution C T missense_variant R65Q 194G>A RECA-EU 1 6159617 6159617 single base substitution C T downstream_gene_variant RECA-EU 1 6181146 6181146 single base substitution G C downstream_gene_variant RECA-EU 1 6181146 6181146 single base substitution G C intron_variant RECA-EU 1 6195872 6195872 single base substitution A T intron_variant RECA-EU 1 6195872 6195872 single base substitution A T upstream_gene_variant RECA-EU 1 6198240 6198240 single base substitution A T intron_variant RECA-EU 1 6215265 6215265 single base substitution G C intron_variant RECA-EU 1 6221830 6221830 single base substitution C A intron_variant RECA-EU 1 6225771 6225771 single base substitution G C intron_variant RECA-EU 1 6235692 6235692 single base substitution C G intron_variant SKCA-BR 1 6158212 6158212 single base substitution C G downstream_gene_variant SKCA-BR 1 6158226 6158226 single base substitution G A downstream_gene_variant SKCA-BR 1 6158923 6158923 single base substitution T A downstream_gene_variant SKCA-BR 1 6159141 6159141 single base substitution C T downstream_gene_variant SKCA-BR 1 6160143 6160143 single base substitution C T downstream_gene_variant SKCA-BR 1 6162206 6162206 single base substitution T C 3_prime_UTR_variant SKCA-BR 1 6162206 6162206 single base substitution T C downstream_gene_variant SKCA-BR 1 6162851 6162851 single base substitution G A 3_prime_UTR_variant SKCA-BR 1 6162851 6162851 single base substitution G A downstream_gene_variant SKCA-BR 1 6163482 6163482 single base substitution T G 3_prime_UTR_variant SKCA-BR 1 6163482 6163482 single base substitution T G downstream_gene_variant SKCA-BR 1 6163816 6163816 single base substitution G A 3_prime_UTR_variant SKCA-BR 1 6163816 6163816 single base substitution G A downstream_gene_variant SKCA-BR 1 6164881 6164881 single base substitution G A 3_prime_UTR_variant SKCA-BR 1 6164881 6164881 single base substitution G A downstream_gene_variant SKCA-BR 1 6166267 6166267 single base substitution A G intron_variant SKCA-BR 1 6167335 6167335 single base substitution G A intron_variant SKCA-BR 1 6167335 6167335 single base substitution G A upstream_gene_variant SKCA-BR 1 6167777 6167777 single base substitution G A intron_variant SKCA-BR 1 6167777 6167777 single base substitution G A upstream_gene_variant SKCA-BR 1 6167780 6167780 single base substitution G A intron_variant SKCA-BR 1 6167780 6167780 single base substitution G A upstream_gene_variant SKCA-BR 1 6167782 6167789 deletion of <=200bp TGGAGGGA - intron_variant SKCA-BR 1 6167782 6167789 deletion of <=200bp TGGAGGGA - upstream_gene_variant SKCA-BR 1 6167834 6167835 deletion of <=200bp TG - intron_variant SKCA-BR 1 6167834 6167835 deletion of <=200bp TG - upstream_gene_variant SKCA-BR 1 6167875 6167875 single base substitution T C intron_variant SKCA-BR 1 6167875 6167875 single base substitution T C upstream_gene_variant SKCA-BR 1 6170379 6170379 single base substitution C T intron_variant SKCA-BR 1 6170379 6170379 single base substitution C T upstream_gene_variant SKCA-BR 1 6170451 6170451 single base substitution G A splice_region_variant SKCA-BR 1 6170451 6170451 single base substitution G A upstream_gene_variant SKCA-BR 1 6171300 6171300 single base substitution G A intron_variant SKCA-BR 1 6171300 6171300 single base substitution G A upstream_gene_variant SKCA-BR 1 6172801 6172801 single base substitution G A intron_variant SKCA-BR 1 6173921 6173921 single base substitution G A intron_variant SKCA-BR 1 6174479 6174479 single base substitution C T intron_variant SKCA-BR 1 6174497 6174497 single base substitution C T intron_variant SKCA-BR 1 6175053 6175053 single base substitution G A intron_variant SKCA-BR 1 6175325 6175325 single base substitution G A intron_variant SKCA-BR 1 6175415 6175415 single base substitution C T intron_variant SKCA-BR 1 6175433 6175433 single base substitution C T intron_variant SKCA-BR 1 6177175 6177175 single base substitution A T intron_variant SKCA-BR 1 6180303 6180303 single base substitution C T intron_variant SKCA-BR 1 6181788 6181788 single base substitution T A downstream_gene_variant SKCA-BR 1 6181788 6181788 single base substitution T A intron_variant SKCA-BR 1 6181916 6181916 single base substitution G A downstream_gene_variant SKCA-BR 1 6181916 6181916 single base substitution G A intron_variant SKCA-BR 1 6181965 6181965 single base substitution G A downstream_gene_variant SKCA-BR 1 6181965 6181965 single base substitution G A intron_variant SKCA-BR 1 6182473 6182473 single base substitution G A downstream_gene_variant SKCA-BR 1 6182473 6182473 single base substitution G A intron_variant SKCA-BR 1 6183999 6183999 single base substitution C T downstream_gene_variant SKCA-BR 1 6183999 6183999 single base substitution C T intron_variant SKCA-BR 1 6184629 6184629 single base substitution G A 3_prime_UTR_variant SKCA-BR 1 6184629 6184629 single base substitution G A downstream_gene_variant SKCA-BR 1 6184629 6184629 single base substitution G A exon_variant SKCA-BR 1 6184629 6184629 single base substitution G A intron_variant SKCA-BR 1 6184629 6184629 single base substitution G A missense_variant S1496F 4487C>T SKCA-BR 1 6184629 6184629 single base substitution G A missense_variant S353F 1058C>T SKCA-BR 1 6184752 6184752 single base substitution G A downstream_gene_variant SKCA-BR 1 6184752 6184752 single base substitution G A intron_variant SKCA-BR 1 6185196 6185196 single base substitution A C 3_prime_UTR_variant SKCA-BR 1 6185196 6185196 single base substitution A C downstream_gene_variant SKCA-BR 1 6185196 6185196 single base substitution A C exon_variant SKCA-BR 1 6185196 6185196 single base substitution A C intron_variant SKCA-BR 1 6185196 6185196 single base substitution A C missense_variant V1453G 4358T>G SKCA-BR 1 6185196 6185196 single base substitution A C missense_variant V310G 929T>G SKCA-BR 1 6185909 6185909 single base substitution T C 3_prime_UTR_variant SKCA-BR 1 6185909 6185909 single base substitution T C exon_variant SKCA-BR 1 6185909 6185909 single base substitution T C intron_variant SKCA-BR 1 6185909 6185909 single base substitution T C missense_variant D1363G 4088A>G SKCA-BR 1 6185909 6185909 single base substitution T C missense_variant D220G 659A>G SKCA-BR 1 6187248 6187248 single base substitution G A intron_variant SKCA-BR 1 6190505 6190505 single base substitution G A intron_variant SKCA-BR 1 6190505 6190505 single base substitution G A upstream_gene_variant SKCA-BR 1 6191983 6191983 single base substitution A C intron_variant SKCA-BR 1 6191983 6191983 single base substitution A C upstream_gene_variant SKCA-BR 1 6192626 6192626 single base substitution G A intron_variant SKCA-BR 1 6192626 6192626 single base substitution G A upstream_gene_variant SKCA-BR 1 6193042 6193042 single base substitution A G intron_variant SKCA-BR 1 6193042 6193042 single base substitution A G upstream_gene_variant SKCA-BR 1 6195244 6195244 single base substitution G A intron_variant SKCA-BR 1 6195244 6195244 single base substitution G A upstream_gene_variant SKCA-BR 1 6195481 6195481 single base substitution G A intron_variant SKCA-BR 1 6195481 6195481 single base substitution G A upstream_gene_variant SKCA-BR 1 6196087 6196088 deletion of <=200bp CA - intron_variant SKCA-BR 1 6196087 6196088 deletion of <=200bp CA - upstream_gene_variant SKCA-BR 1 6196118 6196118 single base substitution C T intron_variant SKCA-BR 1 6196118 6196118 single base substitution C T upstream_gene_variant SKCA-BR 1 6196647 6196647 single base substitution C T 5_prime_UTR_variant SKCA-BR 1 6196647 6196647 single base substitution C T exon_variant SKCA-BR 1 6196647 6196647 single base substitution C T missense_variant G876R 2626G>A SKCA-BR 1 6196647 6196647 single base substitution C T upstream_gene_variant SKCA-BR 1 6197230 6197230 single base substitution G A intron_variant SKCA-BR 1 6197414 6197414 single base substitution A G intron_variant SKCA-BR 1 6199278 6199278 single base substitution C T intron_variant SKCA-BR 1 6199288 6199288 insertion of <=200bp - TTTG intron_variant SKCA-BR 1 6201158 6201158 single base substitution A G intron_variant SKCA-BR 1 6201956 6201956 single base substitution G A intron_variant SKCA-BR 1 6202111 6202111 single base substitution G A intron_variant SKCA-BR 1 6202748 6202748 single base substitution C T intron_variant SKCA-BR 1 6203343 6203343 single base substitution C T intron_variant SKCA-BR 1 6203440 6203440 single base substitution C T intron_variant SKCA-BR 1 6203792 6203792 single base substitution C T intron_variant SKCA-BR 1 6204528 6204528 single base substitution T G intron_variant SKCA-BR 1 6204528 6204528 single base substitution T G upstream_gene_variant SKCA-BR 1 6206555 6206555 single base substitution C T intron_variant SKCA-BR 1 6206555 6206555 single base substitution C T upstream_gene_variant SKCA-BR 1 6207571 6207571 single base substitution A C intron_variant SKCA-BR 1 6207571 6207571 single base substitution A C upstream_gene_variant SKCA-BR 1 6208128 6208128 single base substitution C T intron_variant SKCA-BR 1 6208128 6208128 single base substitution C T upstream_gene_variant SKCA-BR 1 6210527 6210527 single base substitution C T intron_variant SKCA-BR 1 6210533 6210533 single base substitution G A intron_variant SKCA-BR 1 6211587 6211587 single base substitution G C intron_variant SKCA-BR 1 6213415 6213415 single base substitution G C intron_variant SKCA-BR 1 6215212 6215212 insertion of <=200bp - AC intron_variant SKCA-BR 1 6215588 6215588 single base substitution C T intron_variant SKCA-BR 1 6218815 6218815 single base substitution C T intron_variant SKCA-BR 1 6218844 6218844 single base substitution G A intron_variant SKCA-BR 1 6219023 6219023 single base substitution C T intron_variant SKCA-BR 1 6219825 6219825 single base substitution G A intron_variant SKCA-BR 1 6223354 6223354 single base substitution G A intron_variant SKCA-BR 1 6224354 6224354 single base substitution G A intron_variant SKCA-BR 1 6224798 6224798 single base substitution G A intron_variant SKCA-BR 1 6224852 6224852 single base substitution C T intron_variant SKCA-BR 1 6227923 6227923 single base substitution G A intron_variant SKCA-BR 1 6228103 6228103 single base substitution A C intron_variant SKCA-BR 1 6229466 6229466 single base substitution G T intron_variant SKCA-BR 1 6229552 6229552 single base substitution C T intron_variant SKCA-BR 1 6230949 6230949 single base substitution G A intron_variant SKCA-BR 1 6231197 6231197 single base substitution C T intron_variant SKCA-BR 1 6231356 6231356 single base substitution C T intron_variant SKCA-BR 1 6233168 6233169 deletion of <=200bp CT - intron_variant SKCA-BR 1 6234738 6234738 single base substitution G A intron_variant SKCA-BR 1 6234898 6234898 single base substitution G A intron_variant SKCA-BR 1 6235037 6235037 single base substitution G A intron_variant SKCA-BR 1 6235055 6235055 single base substitution A T intron_variant SKCA-BR 1 6235055 6235059 deletion of <=200bp ATGGC - intron_variant SKCA-BR 1 6236704 6236704 single base substitution A C intron_variant SKCA-BR 1 6237287 6237287 single base substitution T G intron_variant SKCA-BR 1 6239247 6239247 single base substitution T C intron_variant SKCM-US 1 6158556 6158556 single base substitution A G downstream_gene_variant SKCM-US 1 6166483 6166483 single base substitution G A 3_prime_UTR_variant SKCM-US 1 6166483 6166483 single base substitution G A intron_variant SKCM-US 1 6166483 6166483 single base substitution G A synonymous_variant N1943N 5829C>T SKCM-US 1 6166762 6166762 single base substitution G A 3_prime_UTR_variant SKCM-US 1 6166762 6166762 single base substitution G A missense_variant P1886S 5656C>T SKCM-US 1 6166762 6166762 single base substitution G A missense_variant P24S 70C>T SKCM-US 1 6166762 6166762 single base substitution G A missense_variant P743S 2227C>T SKCM-US 1 6169886 6169886 single base substitution C T 3_prime_UTR_variant SKCM-US 1 6169886 6169886 single base substitution C T synonymous_variant G1849G 5547G>A SKCM-US 1 6169886 6169886 single base substitution C T synonymous_variant G706G 2118G>A SKCM-US 1 6169886 6169886 single base substitution C T upstream_gene_variant SKCM-US 1 6171884 6171884 single base substitution C T 3_prime_UTR_variant SKCM-US 1 6171884 6171884 single base substitution C T missense_variant D1734N 5200G>A SKCM-US 1 6171884 6171884 single base substitution C T missense_variant D591N 1771G>A SKCM-US 1 6172219 6172219 single base substitution G A 3_prime_UTR_variant SKCM-US 1 6172219 6172219 single base substitution G A synonymous_variant I1707I 5121C>T SKCM-US 1 6172219 6172219 single base substitution G A synonymous_variant I564I 1692C>T SKCM-US 1 6172243 6172243 single base substitution C T 3_prime_UTR_variant SKCM-US 1 6172243 6172243 single base substitution C T synonymous_variant G1699G 5097G>A SKCM-US 1 6172243 6172243 single base substitution C T synonymous_variant G556G 1668G>A SKCM-US 1 6173030 6173030 single base substitution G A 3_prime_UTR_variant SKCM-US 1 6173030 6173030 single base substitution G A exon_variant SKCM-US 1 6173030 6173030 single base substitution G A synonymous_variant I1647I 4941C>T SKCM-US 1 6173030 6173030 single base substitution G A synonymous_variant I504I 1512C>T SKCM-US 1 6181208 6181208 single base substitution C T 3_prime_UTR_variant SKCM-US 1 6181208 6181208 single base substitution C T downstream_gene_variant SKCM-US 1 6181208 6181208 single base substitution C T exon_variant SKCM-US 1 6181208 6181208 single base substitution C T synonymous_variant E1623E 4869G>A SKCM-US 1 6181208 6181208 single base substitution C T synonymous_variant E480E 1440G>A SKCM-US 1 6181214 6181214 single base substitution C T 3_prime_UTR_variant SKCM-US 1 6181214 6181214 single base substitution C T downstream_gene_variant SKCM-US 1 6181214 6181214 single base substitution C T exon_variant SKCM-US 1 6181214 6181214 single base substitution C T synonymous_variant R1621R 4863G>A SKCM-US 1 6181214 6181214 single base substitution C T synonymous_variant R478R 1434G>A SKCM-US 1 6181563 6181563 single base substitution C T 3_prime_UTR_variant SKCM-US 1 6181563 6181563 single base substitution C T downstream_gene_variant SKCM-US 1 6181563 6181563 single base substitution C T exon_variant SKCM-US 1 6181563 6181563 single base substitution C T synonymous_variant L1590L 4770G>A SKCM-US 1 6181563 6181563 single base substitution C T synonymous_variant L447L 1341G>A SKCM-US 1 6184071 6184071 single base substitution C T 3_prime_UTR_variant SKCM-US 1 6184071 6184071 single base substitution C T downstream_gene_variant SKCM-US 1 6184071 6184071 single base substitution C T exon_variant SKCM-US 1 6184071 6184071 single base substitution C T intron_variant SKCM-US 1 6184071 6184071 single base substitution C T missense_variant D1546N 4636G>A SKCM-US 1 6184071 6184071 single base substitution C T missense_variant D403N 1207G>A SKCM-US 1 6184100 6184100 single base substitution C T 3_prime_UTR_variant SKCM-US 1 6184100 6184100 single base substitution C T downstream_gene_variant SKCM-US 1 6184100 6184100 single base substitution C T exon_variant SKCM-US 1 6184100 6184100 single base substitution C T intron_variant SKCM-US 1 6184100 6184100 single base substitution C T missense_variant G1536E 4607G>A SKCM-US 1 6184100 6184100 single base substitution C T missense_variant G393E 1178G>A SKCM-US 1 6184111 6184111 single base substitution C T 3_prime_UTR_variant SKCM-US 1 6184111 6184111 single base substitution C T downstream_gene_variant SKCM-US 1 6184111 6184111 single base substitution C T exon_variant SKCM-US 1 6184111 6184111 single base substitution C T intron_variant SKCM-US 1 6184111 6184111 single base substitution C T synonymous_variant E1532E 4596G>A SKCM-US 1 6184111 6184111 single base substitution C T synonymous_variant E389E 1167G>A SKCM-US 1 6184141 6184141 single base substitution C T 3_prime_UTR_variant SKCM-US 1 6184141 6184141 single base substitution C T downstream_gene_variant SKCM-US 1 6184141 6184141 single base substitution C T exon_variant SKCM-US 1 6184141 6184141 single base substitution C T intron_variant SKCM-US 1 6184141 6184141 single base substitution C T synonymous_variant G1522G 4566G>A SKCM-US 1 6184141 6184141 single base substitution C T synonymous_variant G379G 1137G>A SKCM-US 1 6184666 6184666 single base substitution C T 3_prime_UTR_variant SKCM-US 1 6184666 6184666 single base substitution C T downstream_gene_variant SKCM-US 1 6184666 6184666 single base substitution C T exon_variant SKCM-US 1 6184666 6184666 single base substitution C T intron_variant SKCM-US 1 6184666 6184666 single base substitution C T missense_variant E1484K 4450G>A SKCM-US 1 6184666 6184666 single base substitution C T missense_variant E341K 1021G>A SKCM-US 1 6185624 6185624 single base substitution G A 3_prime_UTR_variant SKCM-US 1 6185624 6185624 single base substitution G A exon_variant SKCM-US 1 6185624 6185624 single base substitution G A intron_variant SKCM-US 1 6185624 6185624 single base substitution G A missense_variant P1407L 4220C>T SKCM-US 1 6185624 6185624 single base substitution G A missense_variant P264L 791C>T SKCM-US 1 6185911 6185911 single base substitution C T 3_prime_UTR_variant SKCM-US 1 6185911 6185911 single base substitution C T exon_variant SKCM-US 1 6185911 6185911 single base substitution C T intron_variant SKCM-US 1 6185911 6185911 single base substitution C T synonymous_variant Q1362Q 4086G>A SKCM-US 1 6185911 6185911 single base substitution C T synonymous_variant Q219Q 657G>A SKCM-US 1 6188166 6188166 single base substitution C T 3_prime_UTR_variant SKCM-US 1 6188166 6188166 single base substitution C T exon_variant SKCM-US 1 6188166 6188166 single base substitution C T intron_variant SKCM-US 1 6188166 6188166 single base substitution C T missense_variant M1281I 3843G>A SKCM-US 1 6188166 6188166 single base substitution C T missense_variant M138I 414G>A SKCM-US 1 6188922 6188922 single base substitution C T 3_prime_UTR_variant SKCM-US 1 6188922 6188922 single base substitution C T exon_variant SKCM-US 1 6188922 6188922 single base substitution C T intron_variant SKCM-US 1 6188922 6188922 single base substitution C T missense_variant E1199K 3595G>A SKCM-US 1 6188922 6188922 single base substitution C T missense_variant E56K 166G>A SKCM-US 1 6188922 6188922 single base substitution C T upstream_gene_variant SKCM-US 1 6188925 6188925 single base substitution C T 3_prime_UTR_variant SKCM-US 1 6188925 6188925 single base substitution C T exon_variant SKCM-US 1 6188925 6188925 single base substitution C T intron_variant SKCM-US 1 6188925 6188925 single base substitution C T missense_variant E1198K 3592G>A SKCM-US 1 6188925 6188925 single base substitution C T missense_variant E55K 163G>A SKCM-US 1 6188925 6188925 single base substitution C T upstream_gene_variant SKCM-US 1 6188931 6188931 single base substitution C T 3_prime_UTR_variant SKCM-US 1 6188931 6188931 single base substitution C T exon_variant SKCM-US 1 6188931 6188931 single base substitution C T intron_variant SKCM-US 1 6188931 6188931 single base substitution C T missense_variant G1196S 3586G>A SKCM-US 1 6188931 6188931 single base substitution C T missense_variant G53S 157G>A SKCM-US 1 6188931 6188931 single base substitution C T upstream_gene_variant SKCM-US 1 6188969 6188969 single base substitution G A 3_prime_UTR_variant SKCM-US 1 6188969 6188969 single base substitution G A exon_variant SKCM-US 1 6188969 6188969 single base substitution G A intron_variant SKCM-US 1 6188969 6188969 single base substitution G A missense_variant S1183F 3548C>T SKCM-US 1 6188969 6188969 single base substitution G A missense_variant S40F 119C>T SKCM-US 1 6188969 6188969 single base substitution G A upstream_gene_variant SKCM-US 1 6189052 6189052 single base substitution C T 3_prime_UTR_variant SKCM-US 1 6189052 6189052 single base substitution C T exon_variant SKCM-US 1 6189052 6189052 single base substitution C T intron_variant SKCM-US 1 6189052 6189052 single base substitution C T synonymous_variant E1155E 3465G>A SKCM-US 1 6189052 6189052 single base substitution C T synonymous_variant E12E 36G>A SKCM-US 1 6189052 6189052 single base substitution C T upstream_gene_variant SKCM-US 1 6189094 6189094 single base substitution C T 5_prime_UTR_variant SKCM-US 1 6189094 6189094 single base substitution C T exon_variant SKCM-US 1 6189094 6189094 single base substitution C T splice_region_variant SKCM-US 1 6189094 6189094 single base substitution C T synonymous_variant K1141K 3423G>A SKCM-US 1 6189094 6189094 single base substitution C T upstream_gene_variant SKCM-US 1 6191793 6191793 single base substitution C T 5_prime_UTR_variant SKCM-US 1 6191793 6191793 single base substitution C T exon_variant SKCM-US 1 6191793 6191793 single base substitution C T missense_variant D1054N 3160G>A SKCM-US 1 6191793 6191793 single base substitution C T upstream_gene_variant SKCM-US 1 6194187 6194187 single base substitution C T splice_donor_variant SKCM-US 1 6194187 6194187 single base substitution C T upstream_gene_variant SKCM-US 1 6194297 6194297 single base substitution C T 5_prime_UTR_variant SKCM-US 1 6194297 6194297 single base substitution C T exon_variant SKCM-US 1 6194297 6194297 single base substitution C T missense_variant G1012D 3035G>A SKCM-US 1 6194297 6194297 single base substitution C T upstream_gene_variant SKCM-US 1 6194852 6194852 single base substitution C T 5_prime_UTR_variant SKCM-US 1 6194852 6194852 single base substitution C T exon_variant SKCM-US 1 6194852 6194852 single base substitution C T missense_variant V980I 2938G>A SKCM-US 1 6194852 6194852 single base substitution C T upstream_gene_variant SKCM-US 1 6194871 6194871 single base substitution G A 5_prime_UTR_variant SKCM-US 1 6194871 6194871 single base substitution G A exon_variant SKCM-US 1 6194871 6194871 single base substitution G A synonymous_variant S973S 2919C>T SKCM-US 1 6194871 6194871 single base substitution G A upstream_gene_variant SKCM-US 1 6195313 6195313 single base substitution C T 5_prime_UTR_variant SKCM-US 1 6195313 6195313 single base substitution C T exon_variant SKCM-US 1 6195313 6195313 single base substitution C T synonymous_variant R949R 2847G>A SKCM-US 1 6195313 6195313 single base substitution C T upstream_gene_variant SKCM-US 1 6195349 6195349 single base substitution G A 5_prime_UTR_variant SKCM-US 1 6195349 6195349 single base substitution G A exon_variant SKCM-US 1 6195349 6195349 single base substitution G A synonymous_variant F937F 2811C>T SKCM-US 1 6195349 6195349 single base substitution G A upstream_gene_variant SKCM-US 1 6195421 6195421 single base substitution C T 5_prime_UTR_variant SKCM-US 1 6195421 6195421 single base substitution C T exon_variant SKCM-US 1 6195421 6195421 single base substitution C T synonymous_variant K913K 2739G>A SKCM-US 1 6195421 6195421 single base substitution C T upstream_gene_variant SKCM-US 1 6202196 6202196 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant SKCM-US 1 6202196 6202196 single base substitution G A exon_variant SKCM-US 1 6202196 6202196 single base substitution G A missense_variant R810C 2428C>T SKCM-US 1 6202197 6202197 single base substitution G A 5_prime_UTR_variant SKCM-US 1 6202197 6202197 single base substitution G A exon_variant SKCM-US 1 6202197 6202197 single base substitution G A synonymous_variant F809F 2427C>T SKCM-US 1 6202251 6202251 single base substitution C T 5_prime_UTR_variant SKCM-US 1 6202251 6202251 single base substitution C T exon_variant SKCM-US 1 6202251 6202251 single base substitution C T synonymous_variant R791R 2373G>A SKCM-US 1 6202331 6202331 single base substitution C T 5_prime_UTR_variant SKCM-US 1 6202331 6202331 single base substitution C T exon_variant SKCM-US 1 6202331 6202331 single base substitution C T missense_variant E765K 2293G>A SKCM-US 1 6202348 6202348 single base substitution G A 5_prime_UTR_variant SKCM-US 1 6202348 6202348 single base substitution G A exon_variant SKCM-US 1 6202348 6202348 single base substitution G A missense_variant S759F 2276C>T SKCM-US 1 6203900 6203900 single base substitution C T 5_prime_UTR_variant SKCM-US 1 6203900 6203900 single base substitution C T exon_variant SKCM-US 1 6203900 6203900 single base substitution C T missense_variant D676N 2026G>A SKCM-US 1 6203924 6203924 single base substitution C T 5_prime_UTR_variant SKCM-US 1 6203924 6203924 single base substitution C T exon_variant SKCM-US 1 6203924 6203924 single base substitution C T missense_variant D668N 2002G>A SKCM-US 1 6203991 6203991 single base substitution C T splice_region_variant SKCM-US 1 6204140 6204140 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant SKCM-US 1 6204140 6204140 single base substitution G A exon_variant SKCM-US 1 6204140 6204140 single base substitution G A synonymous_variant I626I 1878C>T SKCM-US 1 6204202 6204202 single base substitution C T 5_prime_UTR_variant SKCM-US 1 6204202 6204202 single base substitution C T exon_variant SKCM-US 1 6204202 6204202 single base substitution C T missense_variant G606R 1816G>A SKCM-US 1 6204202 6204202 single base substitution C T upstream_gene_variant SKCM-US 1 6206302 6206302 single base substitution C T 5_prime_UTR_variant SKCM-US 1 6206302 6206302 single base substitution C T exon_variant SKCM-US 1 6206302 6206302 single base substitution C T stop_gained W591* 1772G>A SKCM-US 1 6206302 6206302 single base substitution C T upstream_gene_variant SKCM-US 1 6206310 6206310 single base substitution C T 5_prime_UTR_variant SKCM-US 1 6206310 6206310 single base substitution C T exon_variant SKCM-US 1 6206310 6206310 single base substitution C T synonymous_variant K588K 1764G>A SKCM-US 1 6206310 6206310 single base substitution C T upstream_gene_variant SKCM-US 1 6206355 6206355 single base substitution G A 5_prime_UTR_variant SKCM-US 1 6206355 6206355 single base substitution G A exon_variant SKCM-US 1 6206355 6206355 single base substitution G A synonymous_variant P573P 1719C>T SKCM-US 1 6206355 6206355 single base substitution G A upstream_gene_variant SKCM-US 1 6206387 6206387 single base substitution C T 5_prime_UTR_variant SKCM-US 1 6206387 6206387 single base substitution C T exon_variant SKCM-US 1 6206387 6206387 single base substitution C T missense_variant G563S 1687G>A SKCM-US 1 6206387 6206387 single base substitution C T upstream_gene_variant SKCM-US 1 6206398 6206398 single base substitution C T 5_prime_UTR_variant SKCM-US 1 6206398 6206398 single base substitution C T exon_variant SKCM-US 1 6206398 6206398 single base substitution C T missense_variant G559E 1676G>A SKCM-US 1 6206398 6206398 single base substitution C T upstream_gene_variant SKCM-US 1 6206416 6206416 single base substitution G A 5_prime_UTR_variant SKCM-US 1 6206416 6206416 single base substitution G A exon_variant SKCM-US 1 6206416 6206416 single base substitution G A missense_variant P553L 1658C>T SKCM-US 1 6206416 6206416 single base substitution G A upstream_gene_variant SKCM-US 1 6206417 6206417 single base substitution G A 5_prime_UTR_variant SKCM-US 1 6206417 6206417 single base substitution G A exon_variant SKCM-US 1 6206417 6206417 single base substitution G A missense_variant P553S 1657C>T SKCM-US 1 6206417 6206417 single base substitution G A upstream_gene_variant SKCM-US 1 6206765 6206765 single base substitution C T 5_prime_UTR_variant SKCM-US 1 6206765 6206765 single base substitution C T exon_variant SKCM-US 1 6206765 6206765 single base substitution C T missense_variant G517E 1550G>A SKCM-US 1 6206765 6206765 single base substitution C T upstream_gene_variant SKCM-US 1 6209357 6209357 single base substitution C T 5_prime_UTR_variant SKCM-US 1 6209357 6209357 single base substitution C T exon_variant SKCM-US 1 6209357 6209357 single base substitution C T synonymous_variant L370L 1110G>A SKCM-US 1 6209413 6209413 single base substitution C T 5_prime_UTR_variant SKCM-US 1 6209413 6209413 single base substitution C T exon_variant SKCM-US 1 6209413 6209413 single base substitution C T missense_variant G352S 1054G>A SKCM-US 1 6212510 6212510 single base substitution A T 5_prime_UTR_variant SKCM-US 1 6212510 6212510 single base substitution A T exon_variant SKCM-US 1 6212510 6212510 single base substitution A T missense_variant F278I 832T>A SKCM-US 1 6214781 6214781 single base substitution G A 5_prime_UTR_variant SKCM-US 1 6214781 6214781 single base substitution G A exon_variant SKCM-US 1 6214781 6214781 single base substitution G A synonymous_variant V228V 684C>T SKCM-US 1 6214928 6214928 single base substitution G A 5_prime_UTR_variant SKCM-US 1 6214928 6214928 single base substitution G A exon_variant SKCM-US 1 6214928 6214928 single base substitution G A synonymous_variant I179I 537C>T SKCM-US 1 6214931 6214931 single base substitution C T 5_prime_UTR_variant SKCM-US 1 6214931 6214931 single base substitution C T exon_variant SKCM-US 1 6214931 6214931 single base substitution C T synonymous_variant K178K 534G>A SKCM-US 1 6215778 6215778 single base substitution C T splice_acceptor_variant SKCM-US 1 6219501 6219501 single base substitution G A 5_prime_UTR_variant SKCM-US 1 6219501 6219501 single base substitution G A exon_variant SKCM-US 1 6219501 6219501 single base substitution G A synonymous_variant S94S 282C>T SKCM-US 1 6219548 6219548 single base substitution C T 5_prime_UTR_variant SKCM-US 1 6219548 6219548 single base substitution C T exon_variant SKCM-US 1 6219548 6219548 single base substitution C T missense_variant E79K 235G>A SKCM-US 1 6228297 6228297 single base substitution G A 5_prime_UTR_variant SKCM-US 1 6228297 6228297 single base substitution G A exon_variant SKCM-US 1 6228297 6228297 single base substitution G A synonymous_variant F40F 120C>T SKCM-US 1 6228338 6228338 single base substitution C T splice_acceptor_variant STAD-US 1 6169955 6169955 single base substitution G A 3_prime_UTR_variant STAD-US 1 6169955 6169955 single base substitution G A synonymous_variant N1826N 5478C>T STAD-US 1 6169955 6169955 single base substitution G A synonymous_variant N683N 2049C>T STAD-US 1 6169955 6169955 single base substitution G A upstream_gene_variant STAD-US 1 6169960 6169960 single base substitution G A 3_prime_UTR_variant STAD-US 1 6169960 6169960 single base substitution G A missense_variant L1825F 5473C>T STAD-US 1 6169960 6169960 single base substitution G A missense_variant L682F 2044C>T STAD-US 1 6169960 6169960 single base substitution G A upstream_gene_variant STAD-US 1 6170003 6170003 single base substitution C T 3_prime_UTR_variant STAD-US 1 6170003 6170003 single base substitution C T synonymous_variant A1810A 5430G>A STAD-US 1 6170003 6170003 single base substitution C T synonymous_variant A667A 2001G>A STAD-US 1 6170003 6170003 single base substitution C T upstream_gene_variant STAD-US 1 6171885 6171885 single base substitution G A 3_prime_UTR_variant STAD-US 1 6171885 6171885 single base substitution G A synonymous_variant Y1733Y 5199C>T STAD-US 1 6171885 6171885 single base substitution G A synonymous_variant Y590Y 1770C>T STAD-US 1 6172337 6172337 single base substitution T A missense_variant D1668V 5003A>T STAD-US 1 6172337 6172337 single base substitution T A missense_variant D525V 1574A>T STAD-US 1 6172337 6172337 single base substitution T A splice_region_variant STAD-US 1 6181285 6181285 single base substitution C T 3_prime_UTR_variant STAD-US 1 6181285 6181285 single base substitution C T downstream_gene_variant STAD-US 1 6181285 6181285 single base substitution C T exon_variant STAD-US 1 6181285 6181285 single base substitution C T missense_variant A1598T 4792G>A STAD-US 1 6181285 6181285 single base substitution C T missense_variant A455T 1363G>A STAD-US 1 6184073 6184073 single base substitution G A 3_prime_UTR_variant STAD-US 1 6184073 6184073 single base substitution G A downstream_gene_variant STAD-US 1 6184073 6184073 single base substitution G A exon_variant STAD-US 1 6184073 6184073 single base substitution G A intron_variant STAD-US 1 6184073 6184073 single base substitution G A missense_variant S1545L 4634C>T STAD-US 1 6184073 6184073 single base substitution G A missense_variant S402L 1205C>T STAD-US 1 6184642 6184642 single base substitution G A 3_prime_UTR_variant STAD-US 1 6184642 6184642 single base substitution G A downstream_gene_variant STAD-US 1 6184642 6184642 single base substitution G A exon_variant STAD-US 1 6184642 6184642 single base substitution G A intron_variant STAD-US 1 6184642 6184642 single base substitution G A missense_variant R1492W 4474C>T STAD-US 1 6184642 6184642 single base substitution G A missense_variant R349W 1045C>T STAD-US 1 6184676 6184676 single base substitution C T 3_prime_UTR_variant STAD-US 1 6184676 6184676 single base substitution C T downstream_gene_variant STAD-US 1 6184676 6184676 single base substitution C T exon_variant STAD-US 1 6184676 6184676 single base substitution C T intron_variant STAD-US 1 6184676 6184676 single base substitution C T synonymous_variant A1480A 4440G>A STAD-US 1 6184676 6184676 single base substitution C T synonymous_variant A337A 1011G>A STAD-US 1 6186673 6186673 single base substitution C T 3_prime_UTR_variant STAD-US 1 6186673 6186673 single base substitution C T exon_variant STAD-US 1 6186673 6186673 single base substitution C T intron_variant STAD-US 1 6186673 6186673 single base substitution C T missense_variant R1346H 4037G>A STAD-US 1 6186673 6186673 single base substitution C T missense_variant R203H 608G>A STAD-US 1 6188120 6188120 single base substitution C T 3_prime_UTR_variant STAD-US 1 6188120 6188120 single base substitution C T exon_variant STAD-US 1 6188120 6188120 single base substitution C T intron_variant STAD-US 1 6188120 6188120 single base substitution C T missense_variant E1297K 3889G>A STAD-US 1 6188120 6188120 single base substitution C T missense_variant E154K 460G>A STAD-US 1 6188970 6188970 single base substitution A G 3_prime_UTR_variant STAD-US 1 6188970 6188970 single base substitution A G exon_variant STAD-US 1 6188970 6188970 single base substitution A G intron_variant STAD-US 1 6188970 6188970 single base substitution A G missense_variant S1183P 3547T>C STAD-US 1 6188970 6188970 single base substitution A G missense_variant S40P 118T>C STAD-US 1 6188970 6188970 single base substitution A G upstream_gene_variant STAD-US 1 6189026 6189026 single base substitution C T 3_prime_UTR_variant STAD-US 1 6189026 6189026 single base substitution C T exon_variant STAD-US 1 6189026 6189026 single base substitution C T intron_variant STAD-US 1 6189026 6189026 single base substitution C T missense_variant R1164H 3491G>A STAD-US 1 6189026 6189026 single base substitution C T missense_variant R21H 62G>A STAD-US 1 6189026 6189026 single base substitution C T upstream_gene_variant STAD-US 1 6189111 6189111 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant STAD-US 1 6189111 6189111 single base substitution G A exon_variant STAD-US 1 6189111 6189111 single base substitution G A missense_variant R1136C 3406C>T STAD-US 1 6189111 6189111 single base substitution G A upstream_gene_variant STAD-US 1 6189120 6189120 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant STAD-US 1 6189120 6189120 single base substitution G A exon_variant STAD-US 1 6189120 6189120 single base substitution G A missense_variant R1133C 3397C>T STAD-US 1 6189120 6189120 single base substitution G A upstream_gene_variant STAD-US 1 6191747 6191747 single base substitution C T 5_prime_UTR_variant STAD-US 1 6191747 6191747 single base substitution C T exon_variant STAD-US 1 6191747 6191747 single base substitution C T missense_variant R1069Q 3206G>A STAD-US 1 6191747 6191747 single base substitution C T upstream_gene_variant STAD-US 1 6194862 6194862 single base substitution G A 5_prime_UTR_variant STAD-US 1 6194862 6194862 single base substitution G A exon_variant STAD-US 1 6194862 6194862 single base substitution G A synonymous_variant G976G 2928C>T STAD-US 1 6194862 6194862 single base substitution G A upstream_gene_variant STAD-US 1 6196693 6196693 deletion of <=200bp A - 5_prime_UTR_variant STAD-US 1 6196693 6196693 deletion of <=200bp A - exon_variant STAD-US 1 6196693 6196693 deletion of <=200bp A - frameshift_variant F860 STAD-US 1 6196693 6196693 deletion of <=200bp A - upstream_gene_variant STAD-US 1 6202212 6202212 single base substitution A G 5_prime_UTR_variant STAD-US 1 6202212 6202212 single base substitution A G exon_variant STAD-US 1 6202212 6202212 single base substitution A G synonymous_variant S804S 2412T>C STAD-US 1 6202574 6202574 single base substitution C T 5_prime_UTR_variant STAD-US 1 6202574 6202574 single base substitution C T exon_variant STAD-US 1 6202574 6202574 single base substitution C T missense_variant R712H 2135G>A STAD-US 1 6203990 6203990 single base substitution C A splice_region_variant STAD-US 1 6203990 6203990 single base substitution C A stop_gained E646* 1936G>T STAD-US 1 6204099 6204099 single base substitution G A 5_prime_UTR_variant STAD-US 1 6204099 6204099 single base substitution G A exon_variant STAD-US 1 6204099 6204099 single base substitution G A missense_variant A640V 1919C>T STAD-US 1 6204126 6204126 single base substitution A G 5_prime_UTR_variant STAD-US 1 6204126 6204126 single base substitution A G exon_variant STAD-US 1 6204126 6204126 single base substitution A G missense_variant I631T 1892T>C STAD-US 1 6206379 6206379 single base substitution G A 5_prime_UTR_variant STAD-US 1 6206379 6206379 single base substitution G A exon_variant STAD-US 1 6206379 6206379 single base substitution G A synonymous_variant S565S 1695C>T STAD-US 1 6206379 6206379 single base substitution G A upstream_gene_variant STAD-US 1 6206467 6206467 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant STAD-US 1 6206467 6206467 single base substitution G A exon_variant STAD-US 1 6206467 6206467 single base substitution G A missense_variant T536M 1607C>T STAD-US 1 6206467 6206467 single base substitution G A upstream_gene_variant STAD-US 1 6206878 6206878 single base substitution C T 5_prime_UTR_variant STAD-US 1 6206878 6206878 single base substitution C T exon_variant STAD-US 1 6206878 6206878 single base substitution C T synonymous_variant E479E 1437G>A STAD-US 1 6206878 6206878 single base substitution C T upstream_gene_variant STAD-US 1 6208971 6208971 single base substitution G A 5_prime_UTR_variant STAD-US 1 6208971 6208971 single base substitution G A exon_variant STAD-US 1 6208971 6208971 single base substitution G A synonymous_variant C442C 1326C>T STAD-US 1 6208971 6208971 single base substitution G A upstream_gene_variant STAD-US 1 6209392 6209392 single base substitution C T 5_prime_UTR_variant STAD-US 1 6209392 6209392 single base substitution C T exon_variant STAD-US 1 6209392 6209392 single base substitution C T missense_variant D359N 1075G>A STAD-US 1 6209393 6209393 single base substitution G A 5_prime_UTR_variant STAD-US 1 6209393 6209393 single base substitution G A exon_variant STAD-US 1 6209393 6209393 single base substitution G A synonymous_variant C358C 1074C>T STAD-US 1 6212502 6212502 deletion of <=200bp C - 5_prime_UTR_variant STAD-US 1 6212502 6212502 deletion of <=200bp C - exon_variant STAD-US 1 6212502 6212502 deletion of <=200bp C - frameshift_variant G280 STAD-US 1 6212526 6212526 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant STAD-US 1 6212526 6212526 single base substitution G A exon_variant STAD-US 1 6212526 6212526 single base substitution G A synonymous_variant A272A 816C>T STAD-US 1 6214827 6214827 single base substitution A G 5_prime_UTR_variant STAD-US 1 6214827 6214827 single base substitution A G exon_variant STAD-US 1 6214827 6214827 single base substitution A G missense_variant V213A 638T>C STAD-US 1 6215730 6215730 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant STAD-US 1 6215730 6215730 single base substitution G A exon_variant STAD-US 1 6215730 6215730 single base substitution G A synonymous_variant D145D 435C>T STAD-US 1 6215763 6215763 single base substitution C T 5_prime_UTR_variant STAD-US 1 6215763 6215763 single base substitution C T exon_variant STAD-US 1 6215763 6215763 single base substitution C T synonymous_variant S134S 402G>A STAD-US 1 6228223 6228223 single base substitution C T 5_prime_UTR_variant STAD-US 1 6228223 6228223 single base substitution C T exon_variant STAD-US 1 6228223 6228223 single base substitution C T missense_variant R65Q 194G>A THCA-SA 1 6163493 6163493 single base substitution C G 3_prime_UTR_variant THCA-SA 1 6163493 6163493 single base substitution C G downstream_gene_variant THCA-US 1 6194802 6194802 single base substitution G C 5_prime_UTR_variant THCA-US 1 6194802 6194802 single base substitution G C exon_variant THCA-US 1 6194802 6194802 single base substitution G C synonymous_variant P996P 2988C>G THCA-US 1 6194802 6194802 single base substitution G C upstream_gene_variant UCEC-US 1 6166347 6166347 single base substitution T G missense_variant D1953A 5858A>C UCEC-US 1 6166347 6166347 single base substitution T G missense_variant I53L 157A>C UCEC-US 1 6166347 6166347 single base substitution T G missense_variant I772L 2314A>C UCEC-US 1 6166347 6166347 single base substitution T G splice_region_variant UCEC-US 1 6169879 6169879 single base substitution G A 3_prime_UTR_variant UCEC-US 1 6169879 6169879 single base substitution G A missense_variant P1852S 5554C>T UCEC-US 1 6169879 6169879 single base substitution G A missense_variant P709S 2125C>T UCEC-US 1 6169879 6169879 single base substitution G A upstream_gene_variant UCEC-US 1 6170461 6170461 single base substitution C A 3_prime_UTR_variant UCEC-US 1 6170461 6170461 single base substitution C A missense_variant R1792M 5375G>T UCEC-US 1 6170461 6170461 single base substitution C A missense_variant R649M 1946G>T UCEC-US 1 6170461 6170461 single base substitution C A upstream_gene_variant UCEC-US 1 6170467 6170467 single base substitution G A 3_prime_UTR_variant UCEC-US 1 6170467 6170467 single base substitution G A missense_variant A1790V 5369C>T UCEC-US 1 6170467 6170467 single base substitution G A missense_variant A647V 1940C>T UCEC-US 1 6170467 6170467 single base substitution G A upstream_gene_variant UCEC-US 1 6170489 6170489 single base substitution C T 3_prime_UTR_variant UCEC-US 1 6170489 6170489 single base substitution C T missense_variant E1783K 5347G>A UCEC-US 1 6170489 6170489 single base substitution C T missense_variant E640K 1918G>A UCEC-US 1 6170489 6170489 single base substitution C T upstream_gene_variant UCEC-US 1 6172218 6172218 single base substitution C T 3_prime_UTR_variant UCEC-US 1 6172218 6172218 single base substitution C T missense_variant A1708T 5122G>A UCEC-US 1 6172218 6172218 single base substitution C T missense_variant A565T 1693G>A UCEC-US 1 6185184 6185184 single base substitution C T 3_prime_UTR_variant UCEC-US 1 6185184 6185184 single base substitution C T downstream_gene_variant UCEC-US 1 6185184 6185184 single base substitution C T exon_variant UCEC-US 1 6185184 6185184 single base substitution C T intron_variant UCEC-US 1 6185184 6185184 single base substitution C T missense_variant R1457Q 4370G>A UCEC-US 1 6185184 6185184 single base substitution C T missense_variant R314Q 941G>A UCEC-US 1 6185196 6185196 single base substitution A G 3_prime_UTR_variant UCEC-US 1 6185196 6185196 single base substitution A G downstream_gene_variant UCEC-US 1 6185196 6185196 single base substitution A G exon_variant UCEC-US 1 6185196 6185196 single base substitution A G intron_variant UCEC-US 1 6185196 6185196 single base substitution A G missense_variant V1453A 4358T>C UCEC-US 1 6185196 6185196 single base substitution A G missense_variant V310A 929T>C UCEC-US 1 6186679 6186679 single base substitution C T 3_prime_UTR_variant UCEC-US 1 6186679 6186679 single base substitution C T exon_variant UCEC-US 1 6186679 6186679 single base substitution C T intron_variant UCEC-US 1 6186679 6186679 single base substitution C T missense_variant R1344H 4031G>A UCEC-US 1 6186679 6186679 single base substitution C T missense_variant R201H 602G>A UCEC-US 1 6186717 6186717 single base substitution C A 3_prime_UTR_variant UCEC-US 1 6186717 6186717 single base substitution C A exon_variant UCEC-US 1 6186717 6186717 single base substitution C A intron_variant UCEC-US 1 6186717 6186717 single base substitution C A missense_variant Q1331H 3993G>T UCEC-US 1 6186717 6186717 single base substitution C A missense_variant Q188H 564G>T UCEC-US 1 6186791 6186791 deletion of <=200bp C - 3_prime_UTR_variant UCEC-US 1 6186791 6186791 deletion of <=200bp C - exon_variant UCEC-US 1 6186791 6186791 deletion of <=200bp C - frameshift_variant E1307 UCEC-US 1 6186791 6186791 deletion of <=200bp C - frameshift_variant E164 UCEC-US 1 6186791 6186791 deletion of <=200bp C - intron_variant UCEC-US 1 6188584 6188584 single base substitution C A 3_prime_UTR_variant UCEC-US 1 6188584 6188584 single base substitution C A exon_variant UCEC-US 1 6188584 6188584 single base substitution C A intron_variant UCEC-US 1 6188584 6188584 single base substitution C A missense_variant K1235N 3705G>T UCEC-US 1 6188584 6188584 single base substitution C A missense_variant K92N 276G>T UCEC-US 1 6188990 6188990 single base substitution C T 3_prime_UTR_variant UCEC-US 1 6188990 6188990 single base substitution C T exon_variant UCEC-US 1 6188990 6188990 single base substitution C T intron_variant UCEC-US 1 6188990 6188990 single base substitution C T missense_variant G1176D 3527G>A UCEC-US 1 6188990 6188990 single base substitution C T missense_variant G33D 98G>A UCEC-US 1 6188990 6188990 single base substitution C T upstream_gene_variant UCEC-US 1 6189123 6189123 single base substitution T C 5_prime_UTR_variant UCEC-US 1 6189123 6189123 single base substitution T C exon_variant UCEC-US 1 6189123 6189123 single base substitution T C missense_variant S1132G 3394A>G UCEC-US 1 6189123 6189123 single base substitution T C upstream_gene_variant UCEC-US 1 6190296 6190296 single base substitution C T 5_prime_UTR_variant UCEC-US 1 6190296 6190296 single base substitution C T exon_variant UCEC-US 1 6190296 6190296 single base substitution C T missense_variant D1119N 3355G>A UCEC-US 1 6190296 6190296 single base substitution C T upstream_gene_variant UCEC-US 1 6194221 6194221 single base substitution C T 5_prime_UTR_variant UCEC-US 1 6194221 6194221 single base substitution C T exon_variant UCEC-US 1 6194221 6194221 single base substitution C T synonymous_variant R1037R 3111G>A UCEC-US 1 6194221 6194221 single base substitution C T upstream_gene_variant UCEC-US 1 6194862 6194862 single base substitution G A 5_prime_UTR_variant UCEC-US 1 6194862 6194862 single base substitution G A exon_variant UCEC-US 1 6194862 6194862 single base substitution G A synonymous_variant G976G 2928C>T UCEC-US 1 6194862 6194862 single base substitution G A upstream_gene_variant UCEC-US 1 6195336 6195336 single base substitution C T 5_prime_UTR_variant UCEC-US 1 6195336 6195336 single base substitution C T exon_variant UCEC-US 1 6195336 6195336 single base substitution C T missense_variant A942T 2824G>A UCEC-US 1 6195336 6195336 single base substitution C T upstream_gene_variant UCEC-US 1 6195406 6195406 single base substitution C A 5_prime_UTR_variant UCEC-US 1 6195406 6195406 single base substitution C A exon_variant UCEC-US 1 6195406 6195406 single base substitution C A missense_variant K918N 2754G>T UCEC-US 1 6195406 6195406 single base substitution C A upstream_gene_variant UCEC-US 1 6196633 6196633 single base substitution C A 5_prime_UTR_variant UCEC-US 1 6196633 6196633 single base substitution C A exon_variant UCEC-US 1 6196633 6196633 single base substitution C A missense_variant Q880H 2640G>T UCEC-US 1 6196633 6196633 single base substitution C A upstream_gene_variant UCEC-US 1 6196844 6196844 single base substitution C T 5_prime_UTR_variant UCEC-US 1 6196844 6196844 single base substitution C T exon_variant UCEC-US 1 6196844 6196844 single base substitution C T missense_variant E840K 2518G>A UCEC-US 1 6202296 6202296 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 1 6202296 6202296 single base substitution G A exon_variant UCEC-US 1 6202296 6202296 single base substitution G A synonymous_variant Y776Y 2328C>T UCEC-US 1 6203920 6203920 single base substitution T A 5_prime_UTR_variant UCEC-US 1 6203920 6203920 single base substitution T A exon_variant UCEC-US 1 6203920 6203920 single base substitution T A missense_variant D669V 2006A>T UCEC-US 1 6203922 6203922 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 1 6203922 6203922 single base substitution G A exon_variant UCEC-US 1 6203922 6203922 single base substitution G A synonymous_variant D668D 2004C>T UCEC-US 1 6204115 6204115 single base substitution C T 5_prime_UTR_variant UCEC-US 1 6204115 6204115 single base substitution C T exon_variant UCEC-US 1 6204115 6204115 single base substitution C T missense_variant D635N 1903G>A UCEC-US 1 6206455 6206455 single base substitution C T 5_prime_UTR_variant UCEC-US 1 6206455 6206455 single base substitution C T exon_variant UCEC-US 1 6206455 6206455 single base substitution C T missense_variant R540H 1619G>A UCEC-US 1 6206455 6206455 single base substitution C T upstream_gene_variant UCEC-US 1 6206464 6206464 single base substitution A G 5_prime_UTR_variant UCEC-US 1 6206464 6206464 single base substitution A G exon_variant UCEC-US 1 6206464 6206464 single base substitution A G missense_variant V537A 1610T>C UCEC-US 1 6206464 6206464 single base substitution A G upstream_gene_variant UCEC-US 1 6206794 6206794 single base substitution A G 5_prime_UTR_variant UCEC-US 1 6206794 6206794 single base substitution A G exon_variant UCEC-US 1 6206794 6206794 single base substitution A G synonymous_variant P507P 1521T>C UCEC-US 1 6206794 6206794 single base substitution A G upstream_gene_variant UCEC-US 1 6206805 6206805 single base substitution C A 5_prime_UTR_variant UCEC-US 1 6206805 6206805 single base substitution C A exon_variant UCEC-US 1 6206805 6206805 single base substitution C A stop_gained E504* 1510G>T UCEC-US 1 6206805 6206805 single base substitution C A upstream_gene_variant UCEC-US 1 6209115 6209115 single base substitution C T 5_prime_UTR_variant UCEC-US 1 6209115 6209115 single base substitution C T exon_variant UCEC-US 1 6209115 6209115 single base substitution C T stop_gained W394* 1182G>A UCEC-US 1 6209115 6209115 single base substitution C T upstream_gene_variant UCEC-US 1 6209407 6209407 single base substitution C T 5_prime_UTR_variant UCEC-US 1 6209407 6209407 single base substitution C T exon_variant UCEC-US 1 6209407 6209407 single base substitution C T missense_variant E354K 1060G>A UCEC-US 1 6211176 6211176 single base substitution C T 5_prime_UTR_variant UCEC-US 1 6211176 6211176 single base substitution C T exon_variant UCEC-US 1 6211176 6211176 single base substitution C T missense_variant A304T 910G>A UCEC-US 1 6211198 6211198 single base substitution C A 5_prime_UTR_variant UCEC-US 1 6211198 6211198 single base substitution C A exon_variant UCEC-US 1 6211198 6211198 single base substitution C A missense_variant R296S 888G>T UCEC-US 1 6212479 6212479 single base substitution C G 5_prime_UTR_variant UCEC-US 1 6212479 6212479 single base substitution C G exon_variant UCEC-US 1 6212479 6212479 single base substitution C G missense_variant G288A 863G>C UCEC-US 1 6214772 6214772 single base substitution C T 5_prime_UTR_variant UCEC-US 1 6214772 6214772 single base substitution C T exon_variant UCEC-US 1 6214772 6214772 single base substitution C T synonymous_variant P231P 693G>A UCEC-US 1 6219478 6219480 deletion of <=200bp TTC - 5_prime_UTR_variant UCEC-US 1 6219478 6219480 deletion of <=200bp TTC - disruptive_inframe_deletion KK101K UCEC-US 1 6219478 6219480 deletion of <=200bp TTC - exon_variant UCEC-US 1 6219495 6219495 single base substitution A G 5_prime_UTR_variant UCEC-US 1 6219495 6219495 single base substitution A G exon_variant UCEC-US 1 6219495 6219495 single base substitution A G synonymous_variant N96N 288T>C

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand 2492701 COSM3491505 c.120C>T p.F40F Substitution - coding silent 1:6168237-6168237 - J73_T COSM3977793 c.2714T>A p.L905Q Substitution - Missense 1:6135386-6135386 - PA285 COSM1162889 c.4167G>C p.G1389G Substitution - coding silent 1:6125770-6125770 - CSCC-17-T COSM4551101 c.5190G>A p.G1730G Substitution - coding silent 1:6111834-6111834 - SM-4B296 COSM4411564 c.2882A>T p.K961M Substitution - Missense 1:6134848-6134848 - 067T COSM1730371 c.3595G>T p.E1199* Substitution - Nonsense 1:6128862-6128862 - TCGA-FW-A3R5-06 COSM3491453 c.4566G>A p.G1522G Substitution - coding silent 1:6124081-6124081 - TCGA-HU-8602-01 COSM4009178 c.3889G>A p.E1297K Substitution - Missense 1:6128060-6128060 - 1517_PT COSM5754483 c.3109C>T p.R1037W Substitution - Missense 1:6134163-6134163 - TCGA-AX-A0J0-01 COSM911250 c.1903G>A p.D635N Substitution - Missense 1:6144055-6144055 - TCGA-D9-A1JW-06 COSM3491489 c.1657C>T p.P553S Substitution - Missense 1:6146357-6146357 - YUJUBE COSM5381332 c.2387C>T p.S796F Substitution - Missense 1:6142177-6142177 - 53M COSM5594402 c.2380G>A p.E794K Substitution - Missense 1:6142184-6142184 - TCGA-A5-A0GB-01 COSM911243 c.2824G>A p.A942T Substitution - Missense 1:6135276-6135276 - DLD1 COSM911251 c.1619G>A p.R540H Substitution - Missense 1:6146395-6146395 - HCA7 COSM4630175 c.836G>A p.G279E Substitution - Missense 1:6152446-6152446 - Br05X COSM39367 c.5199C>T p.Y1733Y Substitution - coding silent 1:6111825-6111825 - T86 COSM535791 c.3609C>T p.D1203D Substitution - coding silent 1:6128848-6128848 - PCSI_0509_Pa_P_526 COSM426529 c.2845C>T p.R949W Substitution - Missense 1:6135255-6135255 - BCB231T COSM4955737 c.4894C>A p.P1632T Substitution - Missense 1:6121123-6121123 - LUAD-5V8LT COSM400741 c.187G>C p.G63R Substitution - Missense 1:6168170-6168170 - TCGA-HT-8564-01 COSM426531 c.2298C>T p.R766R Substitution - coding silent 1:6142266-6142266 - T578 COSM4672056 c.1731G>A p.K577K Substitution - coding silent 1:6146283-6146283 - TCGA-32-2495-01 COSM3400933 c.1585C>G p.L529V Substitution - Missense 1:6146670-6146670 - T3152 COSM4672048 c.3755G>A p.S1252N Substitution - Missense 1:6128194-6128194 - CSCC-31-T COSM3491483 c.1935G>A p.R645R Substitution - coding silent 1:6143931-6143931 - RK189_C01 COSM1627138 c.1551G>A p.G517G Substitution - coding silent 1:6146704-6146704 - 2521252 COSM5053616 c.2299G>A p.E767K Substitution - Missense 1:6142265-6142265 - RK189_C01 COSM1627137 c.1552C>A p.L518M Substitution - Missense 1:6146703-6146703 - TCGA-BR-6452-01 COSM4009162 c.5003A>T p.D1668V Substitution - Missense 1:6112277-6112277 - YUPAER COSM681583 c.804G>A p.G268G Substitution - coding silent 1:6152478-6152478 - LP6005690-DNA_C02 COSM4412223 c.4261-7C>T p.? Unknown 1:6125240-6125240 - 12T COSM107121 c.5109C>T p.F1703F Substitution - coding silent 1:6112171-6112171 - LUAD-RT-S01702 COSM378860 c.3613G>A p.V1205M Substitution - Missense 1:6128844-6128844 - CSCC-7-T COSM4499591 c.5462C>T p.P1821L Substitution - Missense 1:6109911-6109911 - PT46 COSM5928028 c.5528C>T p.S1843F Substitution - Missense 1:6109845-6109845 - TCGA-D3-A51G-06 COSM3491470 c.3465G>A p.E1155E Substitution - coding silent 1:6128992-6128992 - TCGA-F4-6808-01 COSM1343721 c.2726C>A p.A909D Substitution - Missense 1:6135374-6135374 - Pat_14_A COSM5847107 c.2792G>A p.R931Q Substitution - Missense 1:6135308-6135308 - 2492712 COSM5606429 c.2700C>T p.N900N Substitution - coding silent 1:6135400-6135400 - Au4 COSM5603176 c.2943G>A p.S981S Substitution - coding silent 1:6134787-6134787 - CSCC-30-T COSM4540927 c.2913G>A p.L971L Substitution - coding silent 1:6134817-6134817 - TCGA-D1-A17K-01 COSM356407 c.2928C>T p.G976G Substitution - coding silent 1:6134802-6134802 - 2 COSM4166601 c.5650C>T p.R1884C Substitution - Missense 1:6106708-6106708 - TCGA-36-2552-01 COSM1320965 c.3260A>T p.N1087I Substitution - Missense 1:6131633-6131633 - TCGA-FD-A3B4-01 COSM1296620 c.4635G>A p.S1545S Substitution - coding silent 1:6124012-6124012 - TCGA-76-4928-01 COSM3400928 c.4656C>G p.P1552P Substitution - coding silent 1:6123991-6123991 - COLO678 COSM2237771 c.4599G>A p.G1533G Substitution - coding silent 1:6124048-6124048 - CRC-3 COSM304287 c.4907C>T p.P1636L Substitution - Missense 1:6121110-6121110 - HCT15 COSM911251 c.1619G>A p.R540H Substitution - Missense 1:6146395-6146395 - LUAD_E00522 COSM352928 c.1763A>G p.K588R Substitution - Missense 1:6146251-6146251 - TCGA-EE-A3J5-06 COSM3491497 c.282C>T p.S94S Substitution - coding silent 1:6159441-6159441 - 12T COSM3711885 c.3249C>A p.I1083I Substitution - coding silent 1:6131644-6131644 - TCGA-FS-A1ZA-06 COSM3491469 c.3548C>T p.S1183F Substitution - Missense 1:6128909-6128909 - TCGA-06-0210 COSM2150715 c.3458C>T p.S1153L Substitution - Missense 1:6128999-6128999 - B112 COSM1756879 c.5254G>T p.G1752C Substitution - Missense 1:6110522-6110522 - TCGA-D3-A2JF-06 COSM3491498 c.235G>A p.E79K Substitution - Missense 1:6159488-6159488 - TCGA-24-1464-01 COSM112104 c.1391_1392insC p.L465fs*28 Insertion - Frameshift 1:6146863-6146864 - TCGA-DK-A3IM-01 COSM1296626 c.210G>A p.G70G Substitution - coding silent 1:6159513-6159513 - C086 COSM5528629 c.5334G>A p.K1778K Substitution - coding silent 1:6110442-6110442 - ESCC_54 COSM5631387 c.1768G>C p.E590Q Substitution - Missense 1:6146246-6146246 - B25-Tumor COSM1756881 c.3540G>T p.K1180N Substitution - Missense 1:6128917-6128917 - TCGA-BR-4292-01 COSM2237721 c.5478C>T p.N1826N Substitution - coding silent 1:6109895-6109895 - ESCC_53 COSM5631211 c.406C>A p.Q136K Substitution - Missense 1:6155699-6155699 - TCGA-FS-A4F0-06 COSM3491484 c.1878C>T p.I626I Substitution - coding silent 1:6144080-6144080 - TP_2061 COSM5563075 c.2822C>T p.P941L Substitution - Missense 1:6135278-6135278 - TCGA-CG-5721-01 COSM464827 c.816C>T p.A272A Substitution - coding silent 1:6152466-6152466 - TCGA-18-3409-01 COSM681583 c.804G>A p.G268G Substitution - coding silent 1:6152478-6152478 - TCGA-EE-A2MJ-06 COSM3865927 c.5547G>A p.G1849G Substitution - coding silent 1:6109826-6109826 - T3021 COSM4672041 c.5170C>T p.R1724W Substitution - Missense 1:6111854-6111854 - CSCC-41-T COSM4491435 c.3802C>T p.R1268W Substitution - Missense 1:6128147-6128147 - PT31 COSM5906614 c.5275A>T p.I1759F Substitution - Missense 1:6110501-6110501 - TCGA-CC-A7IK-01 COSM4925070 c.1773G>A p.W591* Substitution - Nonsense 1:6146241-6146241 - HCT-116 COSM1667096 c.3343G>A p.V1115I Substitution - Missense 1:6130248-6130248 - TCGA-AA-3510-01 COSM1343724 c.2080G>A p.D694N Substitution - Missense 1:6142569-6142569 - 2492701 COSM5715432 c.4626G>A p.V1542V Substitution - coding silent 1:6124021-6124021 - TCGA-13-2059-01 COSM1320964 c.2161A>T p.T721S Substitution - Missense 1:6142488-6142488 - TCGA-36-2530-01 COSM1320966 c.5397G>A p.A1799A Substitution - coding silent 1:6109976-6109976 - TCGA-BT-A2LB-01 COSM3790177 c.3417G>A p.Q1139Q Substitution - coding silent 1:6129040-6129040 - SNUH_G73_S1 COSM3751338 c.903C>T p.F301F Substitution - coding silent 1:6151123-6151123 - TCGA-BH-A0HA-01 COSM426527 c.4780G>A p.A1594T Substitution - Missense 1:6121237-6121237 - CSCC-45-T COSM4492481 c.398C>T p.S133F Substitution - Missense 1:6155707-6155707 - TCGA-HC-7211-01 COSM1470350 c.5716C>T p.R1906C Substitution - Missense 1:6106642-6106642 - TCGA-BG-A0VX-01 COSM911259 c.863G>C p.G288A Substitution - Missense 1:6152419-6152419 - TCGA-32-4213-01 COSM3400926 c.5229G>A p.W1743* Substitution - Nonsense 1:6111795-6111795 - C086 COSM5528631 c.2236-1G>A p.? Unknown 1:6142329-6142329 - TCGA-BR-8676-01 COSM4009185 c.2135G>A p.R712H Substitution - Missense 1:6142514-6142514 - ME020T COSM225427 c.4258G>A p.E1420K Substitution - Missense 1:6125526-6125526 - Au5 COSM5605635 c.2735C>T p.S912F Substitution - Missense 1:6135365-6135365 - ZZUFHECRKL-G068T COSM3930836 c.3336G>A p.A1112A Substitution - coding silent 1:6130255-6130255 - YULAN COSM1686927 c.121C>T p.P41S Substitution - Missense 1:6168236-6168236 - TCGA-AP-A0LM-01 COSM911256 c.1060G>A p.E354K Substitution - Missense 1:6149347-6149347 - TCGA-EE-A17X-06 COSM3491490 c.1110G>A p.L370L Substitution - coding silent 1:6149297-6149297 - TCGA-ER-A19Q-06 COSM3491475 c.2919C>T p.S973S Substitution - coding silent 1:6134811-6134811 - ESO-859 COSM1238498 c.4335C>T p.D1445D Substitution - coding silent 1:6125159-6125159 - TCGA-AX-A0J0-01 COSM911238 c.3394A>G p.S1132G Substitution - Missense 1:6129063-6129063 - WSU-HN6 COSM4595357 c.1331A>C p.N444T Substitution - Missense 1:6148906-6148906 - OV207 COSM252437 c.1607C>T p.T536M Substitution - Missense 1:6146407-6146407 - S00539 COSM310082 c.2215C>T p.L739F Substitution - Missense 1:6142434-6142434 - CSCC-41-T COSM4530395 c.1696G>A p.E566K Substitution - Missense 1:6146318-6146318 - CSCC-55-T COSM4496586 c.4787C>T p.P1596L Substitution - Missense 1:6121230-6121230 - ESCC_40 COSM3491473 c.3035G>A p.G1012D Substitution - Missense 1:6134237-6134237 - TCGA-DR-A0ZM-01 COSM460586 c.513C>G p.L171L Substitution - coding silent 1:6154892-6154892 - LUAD-S01357 COSM386029 c.241G>T p.D81Y Substitution - Missense 1:6159482-6159482 - TCGA-B8-4154-01 COSM464829 c.296A>G p.K99R Substitution - Missense 1:6159427-6159427 - TCGA-18-3409-01 COSM681585 c.2045C>T p.P682L Substitution - Missense 1:6142604-6142604 - CSCC-27-T COSM4548090 c.4396G>A p.A1466T Substitution - Missense 1:6124660-6124660 - BD110T COSM5514461 c.813G>A p.T271T Substitution - coding silent 1:6152469-6152469 - TCGA-AP-A0LM-01 COSM911257 c.910G>A p.A304T Substitution - Missense 1:6151116-6151116 - HCC1008 COSM32473 c.355G>A p.D119N Substitution - Missense 1:6159368-6159368 - YUCLAT COSM1686343 c.388-1G>A p.? Unknown 1:6155718-6155718 - TCGA-AD-6965-01 COSM1343718 c.3570C>T p.D1190D Substitution - coding silent 1:6128887-6128887 - I2L-P8-Tumor-Organoid COSM5352599 c.4395-7delA p.? Unknown 1:6124668-6124668 - PD22366a COSM5784341 c.470C>G p.T157R Substitution - Missense 1:6155635-6155635 - BCM723T COSM4950269 c.840delG p.I281fs*185 Deletion - Frameshift 1:6152442-6152442 - TCGA-BR-8384-01 COSM2237871 c.1074C>T p.C358C Substitution - coding silent 1:6149333-6149333 - TCGA-BQ-5878-01 COSM3985171 c.1830C>T p.Y610Y Substitution - coding silent 1:6144128-6144128 - TCGA-E2-A15I-01 COSM3805680 c.4358T>G p.V1453G Substitution - Missense 1:6125136-6125136 - TCGA-EE-A3JD-06 COSM4397509 c.4869G>A p.E1623E Substitution - coding silent 1:6121148-6121148 - 1517_PT COSM5754481 c.3994C>G p.Q1332E Substitution - Missense 1:6126656-6126656 - B109 COSM1756882 c.2141C>G p.S714C Substitution - Missense 1:6142508-6142508 - BCB231T COSM4955737 c.4894C>A p.P1632T Substitution - Missense 1:6121123-6121123 - TCGA-19-4068-01 COSM2156475 c.4895C>T p.P1632L Substitution - Missense 1:6121122-6121122 - TCGA-AP-A059-01 COSM911255 c.1182G>A p.W394* Substitution - Nonsense 1:6149055-6149055 - LOVO COSM4240067 c.3216T>G p.G1072G Substitution - coding silent 1:6131677-6131677 - Au4 COSM5603177 c.2277C>T p.S759S Substitution - coding silent 1:6142287-6142287 - TCGA-AR-A256-01 COSM1474120 c.4740C>A p.D1580E Substitution - Missense 1:6121533-6121533 - TCGA-CM-6676-01 COSM3689790 c.4279C>T p.R1427* Substitution - Nonsense 1:6125215-6125215 - B112-Tumor COSM1756878 c.5255G>T p.G1752V Substitution - Missense 1:6110521-6110521 - I2L-P24Tb-Tumor-Biopsy COSM5352539 c.4395-8delC p.? Unknown 1:6124669-6124669 - B112-Tumor COSM1756879 c.5254G>T p.G1752C Substitution - Missense 1:6110522-6110522 - OSCC-GB_00560111 COSM4883630 c.2901C>A p.N967K Substitution - Missense 1:6134829-6134829 - OCC06PT COSM88525 c.3772G>C p.D1258H Substitution - Missense 1:6128177-6128177 - CSCC-7-T COSM2237854 c.1816G>A p.G606R Substitution - Missense 1:6144142-6144142 - TCGA-BR-A4QL-01 COSM1343730 c.1075G>A p.D359N Substitution - Missense 1:6149332-6149332 - TCGA-HU-A4GU-01 COSM4009190 c.1437G>A p.E479E Substitution - coding silent 1:6146818-6146818 - PD4875a COSM5784999 c.4562A>T p.N1521I Substitution - Missense 1:6124085-6124085 - TCGA-EE-A29E-06 COSM3491452 c.4596G>A p.E1532E Substitution - coding silent 1:6124051-6124051 - DN14043 COSM5961929 c.871-9C>T p.? Unknown 1:6151164-6151164 - PD11757a COSM5770215 c.546C>A p.S182S Substitution - coding silent 1:6154859-6154859 - TC32 COSM4577481 c.5463C>T p.P1821P Substitution - coding silent 1:6109910-6109910 - LUAD-B01970 COSM355916 c.115T>G p.F39V Substitution - Missense 1:6168242-6168242 - sysucc-1838T COSM5763652 c.5740C>A p.Q1914K Substitution - Missense 1:6106618-6106618 - HCC161 COSM3705956 c.2898G>A p.R966R Substitution - coding silent 1:6134832-6134832 - TCGA-FW-A3R5-06 COSM3865937 c.1550G>A p.G517E Substitution - Missense 1:6146705-6146705 - sysucc-274T COSM5475842 c.5757C>A p.S1919S Substitution - coding silent 1:6106495-6106495 - LUAD-5V8LT COSM400740 c.1298C>G p.A433G Substitution - Missense 1:6148939-6148939 - sysucc-1397T COSM5473698 c.3081G>A p.M1027I Substitution - Missense 1:6134191-6134191 - HN_62421 COSM127627 c.108C>T p.F36F Substitution - coding silent 1:6168249-6168249 - p1_I-1 COSM1738211 c.781G>C p.D261H Substitution - Missense 1:6152501-6152501 - ATL056 COSM5705512 c.4298T>A p.L1433Q Substitution - Missense 1:6125196-6125196 - Au1 COSM5596495 c.2918C>T p.S973F Substitution - Missense 1:6134812-6134812 - YUPTER COSM5381337 c.130C>T p.P44S Substitution - Missense 1:6168227-6168227 - TCGA-33-6737-01 COSM681586 c.2122C>T p.L708F Substitution - Missense 1:6142527-6142527 - TCGA-76-6657-01 COSM3400934 c.1029G>A p.Q343Q Substitution - coding silent 1:6149378-6149378 - LUAD-S01467 COSM399414 c.741C>T p.G247G Substitution - coding silent 1:6154664-6154664 - TCGA-D3-A5GN-06 COSM3491484 c.1878C>T p.I626I Substitution - coding silent 1:6144080-6144080 - OSCC-GB_00320111 COSM3711379 c.1218C>A p.G406G Substitution - coding silent 1:6149019-6149019 - SC_9081 COSM2237712 c.5685G>A p.S1895S Substitution - coding silent 1:6106673-6106673 - LIM1899 COSM4640040 c.3587G>A p.G1196D Substitution - Missense 1:6128870-6128870 - LUAD-F00018 COSM339092 c.5183_5184CC>AA p.S1728>? Complex 1:6111840-6111841 - PTC-7C COSM3751338 c.903C>T p.F301F Substitution - coding silent 1:6151123-6151123 - TCGA-CG-4306-01 COSM4009169 c.4440G>A p.A1480A Substitution - coding silent 1:6124616-6124616 - S00539 COSM310081 c.4000G>A p.D1334N Substitution - Missense 1:6126650-6126650 - TCGA-CJ-6030-01 COSM464827 c.816C>T p.A272A Substitution - coding silent 1:6152466-6152466 - HCC119T COSM1602593 c.5675T>C p.L1892P Substitution - Missense 1:6106683-6106683 - TCGA-AX-A0J1-01 COSM911248 c.2006A>T p.D669V Substitution - Missense 1:6143860-6143860 - TCGA-HU-A4G9-01 COSM252437 c.1607C>T p.T536M Substitution - Missense 1:6146407-6146407 - YUAKER COSM1686923 c.5298G>A p.M1766I Substitution - Missense 1:6110478-6110478 - sysucc-1421T COSM5483316 c.2574+9C>T p.? Unknown 1:6136719-6136719 - RK193_C01 COSM3741334 c.1802+3G>T p.? Unknown 1:6146209-6146209 - TCGA-AM-5820-01 COSM426530 c.2379C>T p.N793N Substitution - coding silent 1:6142185-6142185 - BB29T COSM32706 c.133G>A p.V45M Substitution - Missense 1:6168224-6168224 - LIM1899 COSM4640038 c.3746T>C p.V1249A Substitution - Missense 1:6128203-6128203 - OSCC-GB_00120111 COSM3711885 c.3249C>A p.I1083I Substitution - coding silent 1:6131644-6131644 - TCGA-EE-A2MG-06 COSM3491485 c.1772G>A p.W591* Substitution - Nonsense 1:6146242-6146242 - S00539 COSM310082 c.2215C>T p.L739F Substitution - Missense 1:6142434-6142434 - TCGA-DA-A3F8-06 COSM3491453 c.4566G>A p.G1522G Substitution - coding silent 1:6124081-6124081 - CSCC-31-T COSM4548055 c.4386G>A p.K1462K Substitution - coding silent 1:6125108-6125108 - TCGA-BS-A0UJ-01 COSM911228 c.4358T>C p.V1453A Substitution - Missense 1:6125136-6125136 - ccRCC-10 COSM1661126 c.802G>C p.G268R Substitution - Missense 1:6152480-6152480 - TCGA-FW-A3R5-06 COSM3865935 c.2002G>A p.D668N Substitution - Missense 1:6143864-6143864 - TCGA-AA-3502-01 COSM1343729 c.1194C>T p.D398D Substitution - coding silent 1:6149043-6149043 - TCGA-EK-A2RN-01 COSM4009185 c.2135G>A p.R712H Substitution - Missense 1:6142514-6142514 - TCGA-AO-A03M-01 COSM3805675 c.5103C>G p.F1701L Substitution - Missense 1:6112177-6112177 - TCGA-GV-A3JX-01 COSM1296623 c.2469C>G p.L823L Substitution - coding silent 1:6136833-6136833 - TCGA-EE-A29M-06 COSM3491460 c.4220C>T p.P1407L Substitution - Missense 1:6125564-6125564 - T3446 COSM4672051 c.3452G>A p.R1151Q Substitution - Missense 1:6129005-6129005 - TCGA-QB-A6FS-06 COSM3865936 c.1687G>A p.G563S Substitution - Missense 1:6146327-6146327 - 2492711 COSM5606429 c.2700C>T p.N900N Substitution - coding silent 1:6135400-6135400 - 61 COSM5735230 c.751G>A p.G251R Substitution - Missense 1:6152531-6152531 - 2492702 COSM5715432 c.4626G>A p.V1542V Substitution - coding silent 1:6124021-6124021 - TCGA-D9-A148-06 COSM3491446 c.4770G>A p.L1590L Substitution - coding silent 1:6121503-6121503 - K-562 COSM1667097 c.2675T>C p.F892S Substitution - Missense 1:6136538-6136538 - TCGA-A5-A0VP-01 COSM911247 c.2328C>T p.Y776Y Substitution - coding silent 1:6142236-6142236 - TCGA-GN-A26C-01 COSM3491477 c.2811C>T p.F937F Substitution - coding silent 1:6135289-6135289 - TCGA-D9-A3Z1-06 COSM3491505 c.120C>T p.F40F Substitution - coding silent 1:6168237-6168237 - CSCC-20-T COSM4448976 c.1529_1530delAG p.E510fs*40 Deletion - Frameshift 1:6146725-6146726 - 2492721 COSM5719201 c.5807C>T p.P1936L Substitution - Missense 1:6106445-6106445 - TCGA-EW-A3U0-01 COSM3805674 c.5785C>T p.P1929S Substitution - Missense 1:6106467-6106467 - Pat_59_A COSM5847108 c.2204C>T p.T735I Substitution - Missense 1:6142445-6142445 - T3024 COSM4672061 c.109G>T p.D37Y Substitution - Missense 1:6168248-6168248 - TCGA-D1-A103-01 COSM911237 c.3527G>A p.G1176D Substitution - Missense 1:6128930-6128930 - PT14_1 COSM5896525 c.4802G>A p.R1601K Substitution - Missense 1:6121215-6121215 - PT48 COSM5930461 c.5335G>A p.G1779S Substitution - Missense 1:6110441-6110441 - 1517_CLM COSM5754483 c.3109C>T p.R1037W Substitution - Missense 1:6134163-6134163 - ME044T COSM228776 c.5189G>A p.G1730E Substitution - Missense 1:6111835-6111835 - T3535 COSM2237811 c.3267C>T p.P1089P Substitution - coding silent 1:6130324-6130324 - T3021 COSM4388179 c.4861C>T p.R1621W Substitution - Missense 1:6121156-6121156 - T3724 COSM4672044 c.4508G>A p.R1503H Substitution - Missense 1:6124548-6124548 - SNUH_G73_S1 COSM3751337 c.1104A>G p.V368V Substitution - coding silent 1:6149303-6149303 - GC1_T COSM146382 c.1840T>A p.W614R Substitution - Missense 1:6144118-6144118 - TCGA-27-2519-01 COSM3400927 c.5047A>C p.N1683H Substitution - Missense 1:6112233-6112233 - TCGA-D8-A1JK-01 COSM1474119 c.5458C>T p.H1820Y Substitution - Missense 1:6109915-6109915 - Pat_76_B COSM5847098 c.5494G>A p.V1832M Substitution - Missense 1:6109879-6109879 - LUAD-CHTN-MAD06-00490 COSM357920 c.1577T>A p.V526E Substitution - Missense 1:6146678-6146678 - TCGA-EB-A5UN-06 COSM3491494 c.534G>A p.K178K Substitution - coding silent 1:6154871-6154871 - TCGA-E2-A15J-01 COSM177220 c.2315C>T p.A772V Substitution - Missense 1:6142249-6142249 - HCT-15 COSM911251 c.1619G>A p.R540H Substitution - Missense 1:6146395-6146395 - ccRCC-22 COSM1661125 c.3498G>A p.M1166I Substitution - Missense 1:6128959-6128959 - TCGA-09-2049-01 COSM70168 c.3499A>G p.M1167V Substitution - Missense 1:6128958-6128958 - B112 COSM1756878 c.5255G>T p.G1752V Substitution - Missense 1:6110521-6110521 - TCGA-BR-6452-01 COSM4009184 c.2412T>C p.S804S Substitution - coding silent 1:6142152-6142152 - LUAD-5V8LT COSM400739 c.2844C>A p.V948V Substitution - coding silent 1:6135256-6135256 - SC_9008 COSM5352539 c.4395-8delC p.? Unknown 1:6124669-6124669 - LUAD-B00416 COSM331199 c.5649_5650CC>GA p.S1883>? Complex 1:6106708-6106709 - Au8 COSM5606429 c.2700C>T p.N900N Substitution - coding silent 1:6135400-6135400 - TCGA-EL-A3N3-01 COSM3369808 c.2988C>G p.P996P Substitution - coding silent 1:6134742-6134742 - RKO COSM2237865 c.1394T>C p.L465P Substitution - Missense 1:6146861-6146861 - LUAD-S01315 COSM345080 c.4361G>A p.R1454Q Substitution - Missense 1:6125133-6125133 - B109-Tumor COSM1756882 c.2141C>G p.S714C Substitution - Missense 1:6142508-6142508 - TCGA-EE-A29M-06 COSM3491440 c.5097G>A p.G1699G Substitution - coding silent 1:6112183-6112183 - PD4127a COSM159977 c.418G>A p.E140K Substitution - Missense 1:6155687-6155687 - RK079_C01 COSM1627139 c.1469G>T p.G490V Substitution - Missense 1:6146786-6146786 - CSCC-31-T COSM4534745 c.2115G>A p.L705L Substitution - coding silent 1:6142534-6142534 - TCGA-EE-A3JI-06 COSM3491474 c.2938G>A p.V980I Substitution - Missense 1:6134792-6134792 - TCGA-HU-A4G8-01 COSM4009161 c.5199C>T p.Y1733Y Substitution - coding silent 1:6111825-6111825 - TCGA-CG-5718-01 COSM4009181 c.3406C>T p.R1136C Substitution - Missense 1:6129051-6129051 - 6115114 COSM5554721 c.4744G>A p.G1582R Substitution - Missense 1:6121529-6121529 - Au4 COSM911242 c.3111G>A p.R1037R Substitution - coding silent 1:6134161-6134161 - B65-Tumor COSM1748541 c.492C>T p.F164F Substitution - coding silent 1:6155613-6155613 - BD114T COSM5502142 c.690C>A p.P230P Substitution - coding silent 1:6154715-6154715 - TCGA-BH-A0HP-01 COSM3805686 c.402G>A p.S134S Substitution - coding silent 1:6155703-6155703 - LUAD-NYU259 COSM371596 c.568G>T p.A190S Substitution - Missense 1:6154837-6154837 - 35M COSM5580613 c.4115A>G p.Y1372C Substitution - Missense 1:6125822-6125822 - STC246 COSM5053614 c.5287C>T p.P1763S Substitution - Missense 1:6110489-6110489 - TCGA-GN-A266-06 COSM3491451 c.4607G>A p.G1536E Substitution - Missense 1:6124040-6124040 - TCGA-G4-6302-01 COSM3689789 c.4467C>T p.G1489G Substitution - coding silent 1:6124589-6124589 - TCGA-DK-A1A3-01 COSM414826 c.4913-1G>C p.? Unknown 1:6112999-6112999 - TCGA-F1-6177-01 COSM4009183 c.3206G>A p.R1069Q Substitution - Missense 1:6131687-6131687 - LUAD-RT-S01702 COSM378859 c.5431T>C p.Y1811H Substitution - Missense 1:6109942-6109942 - TCGA-AP-A056-01 COSM911251 c.1619G>A p.R540H Substitution - Missense 1:6146395-6146395 - 2492703 COSM3491505 c.120C>T p.F40F Substitution - coding silent 1:6168237-6168237 - 1946219 COSM1197702 c.5810G>A p.G1937E Substitution - Missense 1:6106442-6106442 - TCGA-BS-A0UF-01 COSM911245 c.2640G>T p.Q880H Substitution - Missense 1:6136573-6136573 - T1760 COSM4672053 c.2429G>A p.R810H Substitution - Missense 1:6142135-6142135 - UMC11 COSM2237838 c.2453A>T p.K818I Substitution - Missense 1:6136849-6136849 - 105T COSM1237736 c.994A>C p.I332L Substitution - Missense 1:6151032-6151032 - SH-0622 COSM5018273 c.4328delC p.P1443fs*59 Deletion - Frameshift 1:6125166-6125166 - T1154 COSM1343713 c.5660delC p.P1887fs*14 Deletion - Frameshift 1:6106698-6106698 - PTC-7C COSM4144116 c.4615T>C p.S1539P Substitution - Missense 1:6124032-6124032 - HCC066T COSM5821542 c.503T>A p.L168H Substitution - Missense 1:6155602-6155602 - pfg008T COSM1639929 c.1053G>A p.Q351Q Substitution - coding silent 1:6149354-6149354 - TCGA-AP-A051-01 COSM911223 c.5375G>T p.R1792M Substitution - Missense 1:6110401-6110401 - D-10-0001-T COSM2157524 c.2153G>A p.G718D Substitution - Missense 1:6142496-6142496 - sysucc-1450T COSM5480219 c.2319C>T p.P773P Substitution - coding silent 1:6142245-6142245 - HX13T COSM1602594 c.4779+4T>C p.? Unknown 1:6121490-6121490 - LUAD-E00934 COSM393462 c.3959G>A p.W1320* Substitution - Nonsense 1:6126691-6126691 - R104 COSM308005 c.4330C>T p.Q1444* Substitution - Nonsense 1:6125164-6125164 - TCGA-A2-A0EY-01 COSM426531 c.2298C>T p.R766R Substitution - coding silent 1:6142266-6142266 - ESO-669 COSM252437 c.1607C>T p.T536M Substitution - Missense 1:6146407-6146407 - 1_RESISTANT COSM1718401 c.1842G>A p.W614* Substitution - Nonsense 1:6144116-6144116 - HCC08T COSM131045 c.1972A>G p.R658G Substitution - Missense 1:6143894-6143894 - D28 COSM5544693 c.3234C>G p.L1078L Substitution - coding silent 1:6131659-6131659 - TCGA-KK-A59V-01 COSM4388179 c.4861C>T p.R1621W Substitution - Missense 1:6121156-6121156 - TCGA-BF-A1PX-01 COSM4905369 c.2276C>T p.S759F Substitution - Missense 1:6142288-6142288 - TCGA-ER-A194-01 COSM3491468 c.3586G>A p.G1196S Substitution - Missense 1:6128871-6128871 - SNU-175 COSM2237809 c.3276G>T p.Q1092H Substitution - Missense 1:6130315-6130315 - SS6003312 COSM911247 c.2328C>T p.Y776Y Substitution - coding silent 1:6142236-6142236 - TCGA-A7-A426-01 COSM3805681 c.3234C>A p.L1078L Substitution - coding silent 1:6131659-6131659 - BCM723T COSM4950269 c.840delG p.I281fs*185 Deletion - Frameshift 1:6152442-6152442 - RK119_C01 COSM3741333 c.3118G>T p.G1040W Substitution - Missense 1:6134154-6134154 - B109-Tumor COSM1748538 c.2274C>T p.L758L Substitution - coding silent 1:6142290-6142290 - TCGA-D9-A6EC-06 COSM4401133 c.4450G>A p.E1484K Substitution - Missense 1:6124606-6124606 - TCGA-B0-4836-01 COSM3361627 c.133G>A p.V45M Substitution - Missense 1:6168224-6168224 - T3118 COSM4672059 c.589G>A p.A197T Substitution - Missense 1:6154816-6154816 - 587338 COSM1200983 c.5623G>A p.V1875M Substitution - Missense 1:6106735-6106735 - TCGA-D9-A1JW-06 COSM3491488 c.1658C>T p.P553L Substitution - Missense 1:6146356-6146356 - PTC-7C COSM4144125 c.1235A>T p.E412V Substitution - Missense 1:6149002-6149002 - 2492723 COSM5719201 c.5807C>T p.P1936L Substitution - Missense 1:6106445-6106445 - TCGA-46-3769-01 COSM681595 c.5432A>G p.Y1811C Substitution - Missense 1:6109941-6109941 - Pa07C COSM83866 c.5622C>T p.D1874D Substitution - coding silent 1:6106736-6106736 - TCGA-B5-A11E-01 COSM911242 c.3111G>A p.R1037R Substitution - coding silent 1:6134161-6134161 - 600 COSM3721238 c.290A>G p.K97R Substitution - Missense 1:6159433-6159433 - EGC28 COSM5053617 c.1008C>T p.D336D Substitution - coding silent 1:6149399-6149399 - C086 COSM5528627 c.4708G>A p.E1570K Substitution - Missense 1:6121565-6121565 - 2492720 COSM5719201 c.5807C>T p.P1936L Substitution - Missense 1:6106445-6106445 - CSCC-49-T COSM4565982 c.282_283CC>TT p.P95S Substitution - Missense 1:6159440-6159441 - TCGA-AP-A059-01 COSM911253 c.1521T>C p.P507P Substitution - coding silent 1:6146734-6146734 - TCGA-EE-A3J5-06 COSM3491439 c.5200G>A p.D1734N Substitution - Missense 1:6111824-6111824 - NCI-H2171 COSM27188 c.3917G>T p.R1306L Substitution - Missense 1:6126733-6126733 - BD236T COSM5518097 c.3711G>A p.K1237K Substitution - coding silent 1:6128518-6128518 - TCGA-18-3416-01 COSM681584 c.1701G>T p.K567N Substitution - Missense 1:6146313-6146313 - HCT8 COSM911251 c.1619G>A p.R540H Substitution - Missense 1:6146395-6146395 - B109-Tumor COSM1756880 c.5147A>G p.H1716R Substitution - Missense 1:6111877-6111877 - SJHGG093_D COSM4971699 c.432C>T p.D144D Substitution - coding silent 1:6155673-6155673 - LP6007548-DNA_A01 COSM5952368 c.5444C>T p.T1815M Substitution - Missense 1:6109929-6109929 - TCGA-AP-A059-01 COSM911222 c.5554C>T p.P1852S Substitution - Missense 1:6109819-6109819 - TCGA-AA-3672-01 COSM179381 c.2401G>A p.A801T Substitution - Missense 1:6142163-6142163 - HCC119 COSM1602593 c.5675T>C p.L1892P Substitution - Missense 1:6106683-6106683 - pfg344T COSM4749288 c.1466C>T p.P489L Substitution - Missense 1:6146789-6146789 - ESO-081 COSM1243159 c.5070C>T p.D1690D Substitution - coding silent 1:6112210-6112210 - T2417 COSM4672037 c.5718C>T p.R1906R Substitution - coding silent 1:6106640-6106640 - TP_2034 COSM5555124 c.819G>A p.G273G Substitution - coding silent 1:6152463-6152463 - TCGA-DK-A1AC-01 COSM1296622 c.2817C>T p.N939N Substitution - coding silent 1:6135283-6135283 - TCGA-AY-5543-01 COSM1343715 c.4563C>T p.N1521N Substitution - coding silent 1:6124084-6124084 - ZZUFHECRKL-G033T COSM5437640 c.2235+10C>T p.? Unknown 1:6142404-6142404 - HCC4 COSM1602594 c.4779+4T>C p.? Unknown 1:6121490-6121490 - TCGA-EE-A2MR-06 COSM3491479 c.2428C>T p.R810C Substitution - Missense 1:6142136-6142136 - 217 COSM4424762 c.5551A>T p.K1851* Substitution - Nonsense 1:6109822-6109822 - CSCC-62-T COSM4542613 c.321G>A p.K107K Substitution - coding silent 1:6159402-6159402 - TCGA-BS-A0UA-01 COSM911226 c.5122G>A p.A1708T Substitution - Missense 1:6112158-6112158 - MOLT-4 COSM1667095 c.3814G>A p.A1272T Substitution - Missense 1:6128135-6128135 - 503T COSM4386577 c.2329G>A p.V777M Substitution - Missense 1:6142235-6142235 - TCGA-F4-6463-01 COSM3689791 c.3399C>T p.R1133R Substitution - coding silent 1:6129058-6129058 - TCGA-G3-A25Z-01 COSM4922056 c.2555T>A p.L852H Substitution - Missense 1:6136747-6136747 - HCC4T COSM1602594 c.4779+4T>C p.? Unknown 1:6121490-6121490 - 587376 COSM1200985 c.294G>T p.K98N Substitution - Missense 1:6159429-6159429 - S00539 COSM310081 c.4000G>A p.D1334N Substitution - Missense 1:6126650-6126650 - LUAD-B02594 COSM356407 c.2928C>T p.G976G Substitution - coding silent 1:6134802-6134802 - YUWIA COSM5381334 c.1132C>T p.P378S Substitution - Missense 1:6149275-6149275 - GBM_IV-34 COSM3705957 c.682G>A p.V228I Substitution - Missense 1:6154723-6154723 - TCGA-G2-A2EJ-01 COSM1296624 c.1751G>A p.R584H Substitution - Missense 1:6146263-6146263 - CHC1717T COSM4801973 c.2315C>A p.A772E Substitution - Missense 1:6142249-6142249 - TCGA-AN-A0XR-01 COSM426532 c.1749C>T p.Y583Y Substitution - coding silent 1:6146265-6146265 - RK032_C01 COSM1627136 c.1708A>G p.N570D Substitution - Missense 1:6146306-6146306 - TCGA-CG-4442-01 COSM4009191 c.1326C>T p.C442C Substitution - coding silent 1:6148911-6148911 - I2L-P19Ta-Tumor-Biopsy COSM5352444 c.4395-10_4395-8delCCC p.? Unknown 1:6124669-6124671 - TCGA-BC-A10W-01 COSM4937387 c.3692C>T p.A1231V Substitution - Missense 1:6128537-6128537 - TCGA-FS-A1ZA-06 COSM3491493 c.684C>T p.V228V Substitution - coding silent 1:6154721-6154721 - 8052577 COSM3386264 c.5130G>C p.G1710G Substitution - coding silent 1:6112150-6112150 - 8035823 COSM3386265 c.2865G>A p.M955I Substitution - Missense 1:6135235-6135235 - pfg129T COSM911257 c.910G>A p.A304T Substitution - Missense 1:6151116-6151116 - TCGA-B2-5635-01 COSM464828 c.567T>G p.G189G Substitution - coding silent 1:6154838-6154838 - PT44 COSM5926242 c.2716G>A p.E906K Substitution - Missense 1:6135384-6135384 - T3658 COSM4672057 c.1291T>C p.C431R Substitution - Missense 1:6148946-6148946 - CHC1717T COSM4801973 c.2315C>A p.A772E Substitution - Missense 1:6142249-6142249 - TCGA-F4-6856-01 COSM1343718 c.3570C>T p.D1190D Substitution - coding silent 1:6128887-6128887 - TCGA-BH-A0DZ-01 COSM5832647 c.692_693insC p.Q232fs*61 Insertion - Frameshift 1:6154712-6154713 - TCGA-AM-5820-01 COSM3751337 c.1104A>G p.V368V Substitution - coding silent 1:6149303-6149303 - STC291 COSM5053616 c.2299G>A p.E767K Substitution - Missense 1:6142265-6142265 - YURED COSM1686926 c.1853C>T p.P618L Substitution - Missense 1:6144105-6144105 - TCGA-B5-A11E-01 COSM911249 c.2004C>T p.D668D Substitution - coding silent 1:6143862-6143862 - SNUH_G16_S1 COSM2237803 c.3411C>T p.I1137I Substitution - coding silent 1:6129046-6129046 - 631056 COSM319434 c.5641A>G p.M1881V Substitution - Missense 1:6106717-6106717 - 2492714 COSM5606429 c.2700C>T p.N900N Substitution - coding silent 1:6135400-6135400 - TCGA-AD-6964-01 COSM1343716 c.4441G>A p.D1481N Substitution - Missense 1:6124615-6124615 - HF-23896 COSM1197702 c.5810G>A p.G1937E Substitution - Missense 1:6106442-6106442 - T96 COSM2237731 c.5212C>T p.R1738W Substitution - Missense 1:6111812-6111812 - CSCC-19-T COSM4539161 c.2653G>A p.E885K Substitution - Missense 1:6136560-6136560 - B25 COSM1756881 c.3540G>T p.K1180N Substitution - Missense 1:6128917-6128917 - ESCC_BICR_060T COSM5434920 c.5644C>T p.L1882L Substitution - coding silent 1:6106714-6106714 - NCI-H2171 COSM27188 c.3917G>T p.R1306L Substitution - Missense 1:6126733-6126733 - TCGA-19-4068 COSM2156475 c.4895C>T p.P1632L Substitution - Missense 1:6121122-6121122 - TCGA-AM-5820-01 COSM3751338 c.903C>T p.F301F Substitution - coding silent 1:6151123-6151123 - Pat_06_B COSM5847103 c.3779C>T p.A1260V Substitution - Missense 1:6128170-6128170 - p1_I-2 COSM1738211 c.781G>C p.D261H Substitution - Missense 1:6152501-6152501 - TCGA-EE-A3J5-06 COSM3491461 c.4086G>A p.Q1362Q Substitution - coding silent 1:6125851-6125851 - GC1_T COSM3748482 c.2003A>G p.D668G Substitution - Missense 1:6143863-6143863 - HCT116 COSM2237774 c.4503G>A p.L1501L Substitution - coding silent 1:6124553-6124553 - I2L-P19Ta-Tumor-Organoid COSM5352478 c.4395-9_4395-8delCC p.? Unknown 1:6124669-6124670 - B109 COSM1756880 c.5147A>G p.H1716R Substitution - Missense 1:6111877-6111877 - 32T COSM3711379 c.1218C>A p.G406G Substitution - coding silent 1:6149019-6149019 - T3021 COSM4672037 c.5718C>T p.R1906R Substitution - coding silent 1:6106640-6106640 - 2492700 COSM5715432 c.4626G>A p.V1542V Substitution - coding silent 1:6124021-6124021 - TCGA-EE-A2MU-06 COSM3491472 c.3144+1G>A p.? Unknown 1:6134127-6134127 - NOKSI COSM4595357 c.1331A>C p.N444T Substitution - Missense 1:6148906-6148906 - Pat_41_A COSM2237715 c.5651G>A p.R1884H Substitution - Missense 1:6106707-6106707 - P09-2497 COSM243672 c.5053G>T p.D1685Y Substitution - Missense 1:6112227-6112227 - TCGA-BR-8284-01 COSM4009182 c.3397C>T p.R1133C Substitution - Missense 1:6129060-6129060 - TCGA-AP-A056-01 COSM911236 c.3705G>T p.K1235N Substitution - Missense 1:6128524-6128524 - CSCC-19-T COSM4572677 c.827T>C p.F276S Substitution - Missense 1:6152455-6152455 - DLD1 COSM4623252 c.3659C>A p.P1220H Substitution - Missense 1:6128570-6128570 - OV207 COSM252436 c.5002+2T>G p.? Unknown 1:6112907-6112907 - TCGA-AZ-4315-01 COSM1343714 c.5249+1G>A p.? Unknown 1:6111774-6111774 - TCGA-F1-6875-01 COSM4009167 c.4634C>T p.S1545L Substitution - Missense 1:6124013-6124013 - TCGA-FW-A3R5-06 COSM3865934 c.3423G>A p.K1141K Substitution - coding silent 1:6129034-6129034 - TCGA-FS-A4F5-06 COSM3491441 c.4941C>T p.I1647I Substitution - coding silent 1:6112970-6112970 - CSCC-31-T COSM4478254 c.2222C>T p.S741F Substitution - Missense 1:6142427-6142427 - LUAD-5V8LT COSM400738 c.5503C>G p.L1835V Substitution - Missense 1:6109870-6109870 - TCGA-D5-6928-01 COSM1343728 c.1824G>A p.V608V Substitution - coding silent 1:6144134-6144134 - ZZUFHECRKL-G043T COSM426531 c.2298C>T p.R766R Substitution - coding silent 1:6142266-6142266 - Pat_31_B COSM5847105 c.3332C>T p.T1111M Substitution - Missense 1:6130259-6130259 - PT48 COSM5930459 c.5336G>A p.G1779D Substitution - Missense 1:6110440-6110440 - S02242 COSM5677026 c.3681G>T p.G1227G Substitution - coding silent 1:6128548-6128548 - TCGA-22-1016-01 COSM681596 c.5501G>A p.C1834Y Substitution - Missense 1:6109872-6109872 - TCGA-AC-A23H-01 COSM3805685 c.987G>T p.K329N Substitution - Missense 1:6151039-6151039 - DLD1 COSM4623262 c.930C>T p.S310S Substitution - coding silent 1:6151096-6151096 - CHC2098T COSM4788291 c.5514C>T p.S1838S Substitution - coding silent 1:6109859-6109859 - TCGA-AP-A054-01 COSM911252 c.1610T>C p.V537A Substitution - Missense 1:6146404-6146404 - TCGA-BR-8592-01 COSM356407 c.2928C>T p.G976G Substitution - coding silent 1:6134802-6134802 - SH-0622 COSM5018145 c.5843_5844delGG p.G1948fs*>7 Deletion - Frameshift 1:6106408-6106409 - LUAD-NYU1101 COSM369214 c.2601G>T p.K867N Substitution - Missense 1:6136612-6136612 - 8031121 COSM1158625 c.5319G>A p.K1773K Substitution - coding silent 1:6110457-6110457 - 2492702 COSM3491505 c.120C>T p.F40F Substitution - coding silent 1:6168237-6168237 - PTC-7C COSM3751336 c.1857C>T p.Y619Y Substitution - coding silent 1:6144101-6144101 - CHEWS030 COSM4577483 c.1754A>G p.Y585C Substitution - Missense 1:6146260-6146260 - LP6005500-DNA_D01 COSM1296624 c.1751G>A p.R584H Substitution - Missense 1:6146263-6146263 - TCGA-IR-A3LI-01 COSM4504747 c.673C>T p.P225S Substitution - Missense 1:6154732-6154732 - HCT15 COSM4623252 c.3659C>A p.P1220H Substitution - Missense 1:6128570-6128570 - 1_PRE-TREATMENT COSM1718401 c.1842G>A p.W614* Substitution - Nonsense 1:6144116-6144116 - TCGA-EE-A2ML-06 COSM3491487 c.1719C>T p.P573P Substitution - coding silent 1:6146295-6146295 - 39 COSM3849481 c.1412G>A p.R471Q Substitution - Missense 1:6146843-6146843 - TCGA-BR-4280-01 COSM4009186 c.1936G>T p.E646* Substitution - Nonsense 1:6143930-6143930 - CSCC-20-T COSM4517648 c.3906_3907GG>AA p.E1303K Substitution - Missense 1:6126743-6126744 - YULETA COSM5381333 c.1408C>T p.Q470* Substitution - Nonsense 1:6146847-6146847 - Pat_45_B COSM5847106 c.3262G>A p.A1088T Substitution - Missense 1:6131631-6131631 - T3351 COSM2237800 c.3591G>A p.T1197T Substitution - coding silent 1:6128866-6128866 - Pat_76_A COSM5847098 c.5494G>A p.V1832M Substitution - Missense 1:6109879-6109879 - D-02 COSM4766337 c.3262G>T p.A1088S Substitution - Missense 1:6131631-6131631 - 35M COSM5580612 c.3043G>A p.D1015N Substitution - Missense 1:6134229-6134229 - ME048T COSM229649 c.4241G>A p.R1414Q Substitution - Missense 1:6125543-6125543 - TCGA-GF-A6C9-06 COSM4902635 c.2427C>T p.F809F Substitution - coding silent 1:6142137-6142137 - LUAD-YINHD COSM350088 c.2089G>A p.G697S Substitution - Missense 1:6142560-6142560 - SC_9094 COSM2237724 c.5464G>A p.A1822T Substitution - Missense 1:6109909-6109909 - TCGA-GN-A266-06 COSM3491471 c.3160G>A p.D1054N Substitution - Missense 1:6131733-6131733 - PTC-7C COSM243672 c.5053G>T p.D1685Y Substitution - Missense 1:6112227-6112227 - TCGA-AX-A05S-01 COSM911231 c.3919delG p.E1307fs*94 Deletion - Frameshift 1:6126731-6126731 - CSCC-10-T COSM4493228 c.4119C>T p.S1373S Substitution - coding silent 1:6125818-6125818 - PTC-7C COSM4144111 c.5858A>G p.D1953G Substitution - Missense 1:6106287-6106287 - TCGA-BR-7851-01 COSM4009168 c.4474C>T p.R1492W Substitution - Missense 1:6124582-6124582 - TCGA-43-3394-01 COSM681597 c.5506G>A p.A1836T Substitution - Missense 1:6109867-6109867 - TCGA-AH-6644-01 COSM1560540 c.194G>A p.R65Q Substitution - Missense 1:6168163-6168163 - TCGA-GN-A267-06 COSM3491450 c.4636G>A p.D1546N Substitution - Missense 1:6124011-6124011 - TCGA-AX-A0J0-01 COSM911246 c.2518G>A p.E840K Substitution - Missense 1:6136784-6136784 - TCGA-EI-6917-01 COSM1200984 c.4990G>A p.E1664K Substitution - Missense 1:6112921-6112921 - CSCC-15-T COSM4504747 c.673C>T p.P225S Substitution - Missense 1:6154732-6154732 - 2492713 COSM5606429 c.2700C>T p.N900N Substitution - coding silent 1:6135400-6135400 - TCGA-BR-8081-01 COSM4009193 c.435C>T p.D145D Substitution - coding silent 1:6155670-6155670 - TCGA-GN-A26A-06 COSM3491476 c.2847G>A p.R949R Substitution - coding silent 1:6135253-6135253 - PR-00-1165 COSM243673 c.3398G>A p.R1133H Substitution - Missense 1:6129059-6129059 - TCGA-EE-A2MR-06 COSM3491478 c.2739G>A p.K913K Substitution - coding silent 1:6135361-6135361 - TCGA-FD-A3SS-01 COSM3790173 c.4852C>T p.R1618* Substitution - Nonsense 1:6121165-6121165 - OSCC-GB_01370111 COSM5955650 c.2236-6C>T p.? Unknown 1:6142334-6142334 - RKO COSM911226 c.5122G>A p.A1708T Substitution - Missense 1:6112158-6112158 - TCGA-D3-A3MR-06 COSM3491506 c.80-1G>A p.? Unknown 1:6168278-6168278 - TCGA-AX-A0J0-01 COSM911254 c.1510G>T p.E504* Substitution - Nonsense 1:6146745-6146745 - HT115 COSM369214 c.2601G>T p.K867N Substitution - Missense 1:6136612-6136612 - T3301 COSM4672046 c.4078+2T>C p.? Unknown 1:6126570-6126570 - TCGA-EE-A29E-06 COSM3491505 c.120C>T p.F40F Substitution - coding silent 1:6168237-6168237 - ESO-161 COSM1248216 c.817G>A p.G273R Substitution - Missense 1:6152465-6152465 - TCGA-CM-5344-01 COSM1296620 c.4635G>A p.S1545S Substitution - coding silent 1:6124012-6124012 - PET124T COSM5825367 c.5190G>T p.G1730G Substitution - coding silent 1:6111834-6111834 - TCGA-A5-A0GB-01 COSM911226 c.5122G>A p.A1708T Substitution - Missense 1:6112158-6112158 - TCGA-AP-A0LP-01 COSM911258 c.888G>T p.R296S Substitution - Missense 1:6151138-6151138 - 503LT COSM4386577 c.2329G>A p.V777M Substitution - Missense 1:6142235-6142235 - HCC4T COSM1602592 c.5858-6delT p.? Unknown 1:6106293-6106293 - D-3469-T COSM2157523 c.3978C>G p.H1326Q Substitution - Missense 1:6126672-6126672 - Pat_26_A COSM5847109 c.1330A>T p.N444Y Substitution - Missense 1:6148907-6148907 - TCGA-60-2720-01 COSM681588 c.2661C>T p.F887F Substitution - coding silent 1:6136552-6136552 - TCGA-B5-A0JY-01 COSM911225 c.5347G>A p.E1783K Substitution - Missense 1:6110429-6110429 - CSCC-37-T COSM3491484 c.1878C>T p.I626I Substitution - coding silent 1:6144080-6144080 - TCGA-21-1071-01 COSM681593 c.4161G>A p.P1387P Substitution - coding silent 1:6125776-6125776 - TCGA-DB-5281-01 COSM3966663 c.3973C>T p.R1325W Substitution - Missense 1:6126677-6126677 - TCGA-B0-5098-01 COSM1492117 c.992G>T p.R331M Substitution - Missense 1:6151034-6151034 - TCGA-D1-A17Q-01 COSM911226 c.5122G>A p.A1708T Substitution - Missense 1:6112158-6112158 - TCGA-F1-A448-01 COSM4009192 c.638T>C p.V213A Substitution - Missense 1:6154767-6154767 - NPC16F COSM4995469 c.4603G>A p.E1535K Substitution - Missense 1:6124044-6124044 - TCGA-EE-A2GP-06 COSM3491482 c.2026G>A p.D676N Substitution - Missense 1:6143840-6143840 - TCGA-BR-8687-01 COSM4009159 c.5473C>T p.L1825F Substitution - Missense 1:6109900-6109900 - CADO-ES1 COSM2237841 c.2400C>T p.N800N Substitution - coding silent 1:6142164-6142164 - pfg008T COSM1639928 c.2151G>T p.Q717H Substitution - Missense 1:6142498-6142498 - H2171 COSM310080 c.3917G>T p.R1306L Substitution - Missense 1:6126733-6126733 - T2345 COSM4672060 c.225_226delAT p.S76fs*3 Deletion - Frameshift 1:6159497-6159498 - TCGA-14-0789-01 COSM3400932 c.3484G>T p.A1162S Substitution - Missense 1:6128973-6128973 - TCGA-FS-A1Z3-06 COSM3491466 c.3595G>A p.E1199K Substitution - Missense 1:6128862-6128862 - 9210_T COSM5041887 c.2870+1G>A p.? Unknown 1:6135229-6135229 - Au10 COSM5598139 c.3249C>T p.I1083I Substitution - coding silent 1:6131644-6131644 - T3105 COSM3805686 c.402G>A p.S134S Substitution - coding silent 1:6155703-6155703 - TCGA-JX-A3Q0-01 COSM159979 c.883G>A p.E295K Substitution - Missense 1:6151143-6151143 - 824_T COSM3977794 c.1851G>T p.L617L Substitution - coding silent 1:6144107-6144107 - MDA-MB-231 COSM1683729 c.3214delG p.G1072fs*72 Deletion - Frameshift 1:6131679-6131679 - C086 COSM4551101 c.5190G>A p.G1730G Substitution - coding silent 1:6111834-6111834 - TCGA-AA-3510-01 COSM1343730 c.1075G>A p.D359N Substitution - Missense 1:6149332-6149332 - TCGA-AP-A05N-01 COSM911241 c.3237G>A p.R1079R Substitution - coding silent 1:6131656-6131656 - S43_post COSM911229 c.4031G>A p.R1344H Substitution - Missense 1:6126619-6126619 - T3091 COSM4672054 c.2320G>A p.D774N Substitution - Missense 1:6142244-6142244 - TCGA-D8-A1JK-01 COSM5224052 c.2927delG p.G976fs*11 Deletion - Frameshift 1:6134803-6134803 - pfg125T COSM4749287 c.2033C>T p.P678L Substitution - Missense 1:6143833-6143833 - TCGA-AN-A046-01 COSM3805682 c.3166C>A p.L1056M Substitution - Missense 1:6131727-6131727 - AOCS-161-1-9 COSM3944210 c.4172-4C>G p.? Unknown 1:6125616-6125616 - SW48 COSM1343720 c.2927_2928insG p.G977fs*63 Insertion - Frameshift 1:6134802-6134803 - B71-Tumor COSM3930836 c.3336G>A p.A1112A Substitution - coding silent 1:6130255-6130255 - PTC-77C COSM4144118 c.4047C>T p.V1349V Substitution - coding silent 1:6126603-6126603 - ICC013T COSM5814173 c.3866A>T p.K1289M Substitution - Missense 1:6128083-6128083 - TCGA-E2-A10C-01 COSM426529 c.2845C>T p.R949W Substitution - Missense 1:6135255-6135255 - sysucc-1370T COSM5470452 c.2316G>A p.A772A Substitution - coding silent 1:6142248-6142248 - TCGA-BS-A0UF-01 COSM911244 c.2754G>T p.K918N Substitution - Missense 1:6135346-6135346 - HX13T COSM1602592 c.5858-6delT p.? Unknown 1:6106293-6106293 - TCGA-EE-A2A0-06 COSM3491486 c.1764G>A p.K588K Substitution - coding silent 1:6146250-6146250 - LUAD-NYU408 COSM373888 c.4477G>T p.E1493* Substitution - Nonsense 1:6124579-6124579 - 2492722 COSM5719201 c.5807C>T p.P1936L Substitution - Missense 1:6106445-6106445 - TCGA-BG-A0VW-01 COSM911264 c.303_305delGAA p.K102delK Deletion - In frame 1:6159418-6159420 - TCGA-GN-A266-06 COSM3491491 c.1054G>A p.G352S Substitution - Missense 1:6149353-6149353 - TCGA-D9-A3Z1-06 COSM3491438 c.5656C>T p.P1886S Substitution - Missense 1:6106702-6106702 - TCGA-AM-5821-01 COSM3751336 c.1857C>T p.Y619Y Substitution - coding silent 1:6144101-6144101 - CSCC-20-T COSM4538957 c.2627G>A p.G876E Substitution - Missense 1:6136586-6136586 - TCGA-GD-A3OQ-01 COSM1296621 c.3600C>G p.L1200L Substitution - coding silent 1:6128857-6128857 - B65 COSM1748541 c.492C>T p.F164F Substitution - coding silent 1:6155613-6155613 - pfg008T COSM1639928 c.2151G>T p.Q717H Substitution - Missense 1:6142498-6142498 - HCC058T COSM5804398 c.1637A>T p.N546I Substitution - Missense 1:6146377-6146377 - GHE0624 COSM5714307 c.5705G>A p.R1902H Substitution - Missense 1:6106653-6106653 - TCGA-DK-A3IK-01 COSM1296625 c.559G>A p.V187I Substitution - Missense 1:6154846-6154846 - S0029 COSM5881766 c.2635C>T p.L879F Substitution - Missense 1:6136578-6136578 - TCGA-EE-A2GI-06 COSM3491481 c.2293G>A p.E765K Substitution - Missense 1:6142271-6142271 - 49M COSM3491481 c.2293G>A p.E765K Substitution - Missense 1:6142271-6142271 - PAPNNX COSM5004909 c.4887G>A p.P1629P Substitution - coding silent 1:6121130-6121130 - T3091 COSM4672058 c.675G>A p.P225P Substitution - coding silent 1:6154730-6154730 - TCGA-C4-A0EZ-01 COSM414825 c.1509G>A p.L503L Substitution - coding silent 1:6146746-6146746 - 12M COSM5577339 c.5160G>A p.Q1720Q Substitution - coding silent 1:6111864-6111864 - CSCC-40-T COSM4562555 c.931G>A p.V311M Substitution - Missense 1:6151095-6151095 - T44 COSM5342716 c.577C>T p.R193W Substitution - Missense 1:6154828-6154828 - HCC161T COSM3705956 c.2898G>A p.R966R Substitution - coding silent 1:6134832-6134832 - TCGA-BS-A0UF-01 COSM911229 c.4031G>A p.R1344H Substitution - Missense 1:6126619-6126619 - PD11357a COSM1503521 c.1750C>T p.R584C Substitution - Missense 1:6146264-6146264 - TCGA-G4-6626-01 COSM1343723 c.2268G>A p.A756A Substitution - coding silent 1:6142296-6142296 - TCGA-D3-A2J8-06 COSM1503520 c.1676G>A p.G559E Substitution - Missense 1:6146338-6146338 - HCC126T COSM5818820 c.4358T>A p.V1453E Substitution - Missense 1:6125136-6125136 - TCGA-B5-A11N-01 COSM911221 c.5858A>C p.D1953A Substitution - Missense 1:6106287-6106287 - TCGA-A6-5665-01 COSM1343720 c.2927_2928insG p.G977fs*63 Insertion - Frameshift 1:6134802-6134803 - PR-04-639 COSM243674 c.3872C>T p.A1291V Substitution - Missense 1:6128077-6128077 - PTC-28C COSM4144123 c.1508T>C p.L503P Substitution - Missense 1:6146747-6146747 - STC252 COSM5053619 c.105C>A p.A35A Substitution - coding silent 1:6168252-6168252 - LUAD-F00089 COSM339744 c.557C>T p.T186I Substitution - Missense 1:6154848-6154848 - LUAD-F00257 COSM366886 c.2788A>T p.R930W Substitution - Missense 1:6135312-6135312 - RK261_C01 COSM4778673 c.4172-9G>T p.? Unknown 1:6125621-6125621 - ESO-157 COSM1248215 c.528C>A p.N176K Substitution - Missense 1:6154877-6154877 - TCGA-EE-A2MR-06 COSM3491465 c.3843G>A p.M1281I Substitution - Missense 1:6128106-6128106 - TCGA-CM-4746-01 COSM179392 c.812C>T p.T271M Substitution - Missense 1:6152470-6152470 - TCGA-CJ-6031-01 COSM464826 c.1332C>A p.N444K Substitution - Missense 1:6148905-6148905 - BD241T COSM3849481 c.1412G>A p.R471Q Substitution - Missense 1:6146843-6146843 - TCGA-HU-A4H4-01 COSM1560540 c.194G>A p.R65Q Substitution - Missense 1:6168163-6168163 - TCGA-56-6546-01 COSM681591 c.3031A>G p.N1011D Substitution - Missense 1:6134241-6134241 - YUOTHO COSM5381330 c.3325C>T p.L1109L Substitution - coding silent 1:6130266-6130266 - TCGA-B5-A11E-01 COSM911230 c.3993G>T p.Q1331H Substitution - Missense 1:6126657-6126657 - 2012-705:2012-1310-T COSM4604836 c.238G>A p.E80K Substitution - Missense 1:6159485-6159485 - YUBER COSM1686924 c.4927G>A p.E1643K Substitution - Missense 1:6112984-6112984 - T3011 COSM4672039 c.5667C>T p.A1889A Substitution - coding silent 1:6106691-6106691 - TCGA-HC-7079-01 COSM3671805 c.3302G>T p.R1101L Substitution - Missense 1:6130289-6130289 - TCGA-BR-8363-01 COSM2237871 c.1074C>T p.C358C Substitution - coding silent 1:6149333-6149333 - 2492700 COSM3491505 c.120C>T p.F40F Substitution - coding silent 1:6168237-6168237 - 0006_CRUK_PC_0006_T2_DNA COSM3849481 c.1412G>A p.R471Q Substitution - Missense 1:6146843-6146843 - 202_T COSM3977792 c.5003A>G p.D1668G Substitution - Missense 1:6112277-6112277 - S02290 COSM5686380 c.2625A>G p.T875T Substitution - coding silent 1:6136588-6136588 - 8052570 COSM3771789 c.2870+10G>A p.? Unknown 1:6135220-6135220 - TCGA-EE-A29V-06 COSM3491480 c.2373G>A p.R791R Substitution - coding silent 1:6142191-6142191 - sysucc-783T COSM5483990 c.3262+2T>C p.? Unknown 1:6131629-6131629 - RW7213 COSM4649908 c.3999G>A p.E1333E Substitution - coding silent 1:6126651-6126651 - CHC2098T COSM4788291 c.5514C>T p.S1838S Substitution - coding silent 1:6109859-6109859 - XHDG18 COSM4768742 c.5250G>T p.T1750T Substitution - coding silent 1:6110526-6110526 - MO_1012 COSM5554849 c.5722G>A p.G1908R Substitution - Missense 1:6106636-6106636 - TCGA-A2-A0T5-01 COSM3805684 c.1934+2T>G p.? Unknown 1:6144022-6144022 - HCC005T COSM5808951 c.2976C>T p.C992C Substitution - coding silent 1:6134754-6134754 - HX32T COSM3705957 c.682G>A p.V228I Substitution - Missense 1:6154723-6154723 - T3262 COSM4672055 c.2106G>A p.P702P Substitution - coding silent 1:6142543-6142543 - 587376 COSM1200984 c.4990G>A p.E1664K Substitution - Missense 1:6112921-6112921 - TCGA-IR-A3LA-01 COSM4845428 c.5475C>G p.L1825L Substitution - coding silent 1:6109898-6109898 - LUAD-NYU947 COSM377012 c.1887C>T p.I629I Substitution - coding silent 1:6144071-6144071 - MX02 COSM5352539 c.4395-8delC p.? Unknown 1:6124669-6124669 - C086 COSM4530395 c.1696G>A p.E566K Substitution - Missense 1:6146318-6146318 - PT33 COSM5891578 c.929C>T p.S310F Substitution - Missense 1:6151097-6151097 - TCGA-CG-5721-01 COSM4009187 c.1919C>T p.A640V Substitution - Missense 1:6144039-6144039 - ESO-0001 COSM535791 c.3609C>T p.D1203D Substitution - coding silent 1:6128848-6128848 - TCGA-EE-A29V-06 COSM3491483 c.1935G>A p.R645R Substitution - coding silent 1:6143931-6143931 - CSCC-27-T COSM4500835 c.5747C>T p.A1916V Substitution - Missense 1:6106505-6106505 - 1N26-VS-1T26 COSM4973441 c.3374A>T p.H1125L Substitution - Missense 1:6130217-6130217 - TCGA-D3-A51R-06 COSM3491467 c.3592G>A p.E1198K Substitution - Missense 1:6128865-6128865 - 8066852 COSM3771790 c.2804A>G p.D935G Substitution - Missense 1:6135296-6135296 - CSCC-62-T COSM4549488 c.4746G>A p.G1582G Substitution - coding silent 1:6121527-6121527 - TCGA-CD-A4MG-01 COSM4009160 c.5430G>A p.A1810A Substitution - coding silent 1:6109943-6109943 - TCGA-AU-6004-01 COSM1343722 c.2551C>T p.R851C Substitution - Missense 1:6136751-6136751 - TCGA-ER-A193-06 COSM2237854 c.1816G>A p.G606R Substitution - Missense 1:6144142-6144142 - 030T COSM1728345 c.3709A>C p.K1237Q Substitution - Missense 1:6128520-6128520 - SJBALL021521_D1 COSM2237811 c.3267C>T p.P1089P Substitution - coding silent 1:6130324-6130324 - 2521252 COSM911224 c.5369C>T p.A1790V Substitution - Missense 1:6110407-6110407 - BZ10 COSM5352539 c.4395-8delC p.? Unknown 1:6124669-6124669 - HCC3T COSM1602596 c.1803-10C>T p.? Unknown 1:6144165-6144165 - TCGA-EE-A29D-06 COSM3491473 c.3035G>A p.G1012D Substitution - Missense 1:6134237-6134237 - CLL073 COSM1290218 c.1504C>T p.P502S Substitution - Missense 1:6146751-6146751 - TCGA-BF-A1PX-01 COSM4905421 c.5121C>T p.I1707I Substitution - coding silent 1:6112159-6112159 - SNUH_G73_S1 COSM2237825 c.2944C>T p.L982L Substitution - coding silent 1:6134786-6134786 - TCGA-61-2095-01 COSM111957 c.3969_3970insAT p.L1324fs*78 Insertion - Frameshift 1:6126680-6126681 - TCGA-AA-3956-01 COSM297098 c.3813C>T p.D1271D Substitution - coding silent 1:6128136-6128136 - CSCC-52-T COSM4501222 c.5837C>T p.P1946L Substitution - Missense 1:6106415-6106415 - T3116 COSM1296620 c.4635G>A p.S1545S Substitution - coding silent 1:6124012-6124012 - TCGA-DI-A1NN-01 COSM911227 c.4370G>A p.R1457Q Substitution - Missense 1:6125124-6125124 - TCGA-D1-A167-01 COSM911260 c.693G>A p.P231P Substitution - coding silent 1:6154712-6154712 - SW480 COSM4655702 c.4051T>G p.Y1351D Substitution - Missense 1:6126599-6126599 - 2521262 COSM5891578 c.929C>T p.S310F Substitution - Missense 1:6151097-6151097 - 2492703 COSM5715432 c.4626G>A p.V1542V Substitution - coding silent 1:6124021-6124021 - SS6003311 COSM911247 c.2328C>T p.Y776Y Substitution - coding silent 1:6142236-6142236 - TCGA-HU-A4GQ-01 COSM4009188 c.1892T>C p.I631T Substitution - Missense 1:6144066-6144066 - CHC1601T COSM4805116 c.2235+1G>A p.? Unknown 1:6142413-6142413 - PD4968a COSM5768551 c.5250-7C>T p.? Unknown 1:6110533-6110533 - TCGA-BR-7707-01 COSM4009179 c.3547T>C p.S1183P Substitution - Missense 1:6128910-6128910 - ME045T COSM229415 c.3053C>T p.S1018F Substitution - Missense 1:6134219-6134219 - TCGA-FW-A3R5-06 COSM3865926 c.5829C>T p.N1943N Substitution - coding silent 1:6106423-6106423 - Pat_26_B COSM5847109 c.1330A>T p.N444Y Substitution - Missense 1:6148907-6148907 - OV207 COSM252976 c.3684delG p.N1229fs*26 Deletion - Frameshift 1:6128545-6128545 - TCGA-B5-A11E-01 COSM911240 c.3355G>A p.D1119N Substitution - Missense 1:6130236-6130236 - PD4197a COSM159978 c.3439C>T p.R1147C Substitution - Missense 1:6129018-6129018 - CSCC-15-T COSM4570143 c.2390T>G p.F797C Substitution - Missense 1:6142174-6142174 - S02242 COSM5677028 c.994+1G>A p.? Unknown 1:6151031-6151031 - LP6007546-DNA_A01 COSM5952221 c.4230G>A p.P1410P Substitution - coding silent 1:6125554-6125554 - LAU165 COSM232033 c.4606G>A p.G1536R Substitution - Missense 1:6124041-6124041 - OSCC-GB_00820111 COSM4887295 c.3899G>T p.G1300V Substitution - Missense 1:6128050-6128050 - ME100L COSM230841 c.1819G>A p.D607N Substitution - Missense 1:6144139-6144139 - TCGA-GF-A6C9-06 COSM3491484 c.1878C>T p.I626I Substitution - coding silent 1:6144080-6144080 - PD4939a COSM159979 c.883G>A p.E295K Substitution - Missense 1:6151143-6151143 - TCGA-FP-A4BE-01 COSM4009171 c.4037G>A p.R1346H Substitution - Missense 1:6126613-6126613 - LUAD-YINHD COSM350087 c.2796C>G p.L932L Substitution - coding silent 1:6135304-6135304 - CSCC-7-T COSM4481891 c.2556C>G p.L852L Substitution - coding silent 1:6136746-6136746 - HCC066T COSM5821189 c.3342T>A p.T1114T Substitution - coding silent 1:6130249-6130249 - RK023_C01 COSM1627135 c.3146T>G p.M1049R Substitution - Missense 1:6131747-6131747 - YUZINO COSM1686925 c.4732G>A p.E1578K Substitution - Missense 1:6121541-6121541 - TCGA-B5-A11E-01 COSM911265 c.288T>C p.N96N Substitution - coding silent 1:6159435-6159435 - 266 COSM97935 c.898G>C p.D300H Substitution - Missense 1:6151128-6151128 - 16 COSM3735348 c.2924G>A p.G975E Substitution - Missense 1:6134806-6134806 - TCGA-AX-A05Z-01 COSM911245 c.2640G>T p.Q880H Substitution - Missense 1:6136573-6136573 - ESO-085 COSM1248214 c.4603G>T p.E1535* Substitution - Nonsense 1:6124044-6124044 - CSCC-27-T COSM4544685 c.3618G>T p.E1206D Substitution - Missense 1:6128839-6128839 - 600 COSM911246 c.2518G>A p.E840K Substitution - Missense 1:6136784-6136784 - 2_RESISTANT COSM1721701 c.5736C>T p.I1912I Substitution - coding silent 1:6106622-6106622 - TCGA-BH-A0B6-01 COSM3805683 c.2927G>A p.G976D Substitution - Missense 1:6134803-6134803 - TCGA-EJ-7125-01 COSM3671806 c.132C>A p.P44P Substitution - coding silent 1:6168225-6168225 - 8068577 COSM4388179 c.4861C>T p.R1621W Substitution - Missense 1:6121156-6121156 - PT46 COSM5928030 c.2260G>A p.V754I Substitution - Missense 1:6142304-6142304 - CSCC-44-T COSM4517178 c.2924_2925GG>AA p.G975E Substitution - Missense 1:6134805-6134806 - TCGA-B0-4837-01 COSM3360975 c.5198A>G p.Y1733C Substitution - Missense 1:6111826-6111826 - CPCG0374-F1 COSM4966611 c.3504C>G p.L1168L Substitution - coding silent 1:6128953-6128953 - YUSMI COSM5381331 c.2415G>A p.G805G Substitution - coding silent 1:6142149-6142149 - HCC099T COSM5816577 c.5743-4C>G p.? Unknown 1:6106513-6106513 - CSCC-56-T COSM4497055 c.4893C>T p.S1631S Substitution - coding silent 1:6121124-6121124 - HCC36T COSM1602595 c.4395-7A>C p.? Unknown 1:6124668-6124668 - TCGA-DM-A28K-01 COSM1343729 c.1194C>T p.D398D Substitution - coding silent 1:6149043-6149043 - 587278 COSM386029 c.241G>T p.D81Y Substitution - Missense 1:6159482-6159482 - TCGA-AP-A0LM-01 COSM911224 c.5369C>T p.A1790V Substitution - Missense 1:6110407-6110407 - TCGA-BR-4362-01 COSM3805686 c.402G>A p.S134S Substitution - coding silent 1:6155703-6155703 - LUAD_E00565 COSM388819 c.4504A>T p.T1502S Substitution - Missense 1:6124552-6124552 - B109 COSM1748538 c.2274C>T p.L758L Substitution - coding silent 1:6142290-6142290 - PTC-28C COSM4144124 c.1506C>T p.P502P Substitution - coding silent 1:6146749-6146749 - TCGA-HC-8216-01 COSM3671807 c.106T>A p.F36I Substitution - Missense 1:6168251-6168251 - pfg413T COSM4749279 c.4286G>A p.R1429Q Substitution - Missense 1:6125208-6125208 - pfg062T COSM4749281 c.4028A>T p.K1343M Substitution - Missense 1:6126622-6126622 - TCGA-GF-A6C9-06 COSM4902644 c.537C>T p.I179I Substitution - coding silent 1:6154868-6154868 - BD236T COSM4905421 c.5121C>T p.I1707I Substitution - coding silent 1:6112159-6112159 - BB23T COSM33237 c.1999A>G p.R667G Substitution - Missense 1:6143867-6143867 - TCGA-06-0210-02 COSM2150715 c.3458C>T p.S1153L Substitution - Missense 1:6128999-6128999 - CHC1601T COSM4805116 c.2235+1G>A p.? Unknown 1:6142413-6142413 - C086 COSM3491505 c.120C>T p.F40F Substitution - coding silent 1:6168237-6168237 - CSCC-27-T COSM4483583 c.2713C>T p.L905L Substitution - coding silent 1:6135387-6135387 - BD72T COSM5511449 c.5858-7_5858-6insT p.? Unknown 1:6106293-6106294 - TCGA-FS-A1ZC-06 COSM3491445 c.4863G>A p.R1621R Substitution - coding silent 1:6121154-6121154 - TCGA-HU-A4G9-01 COSM4009163 c.4792G>A p.A1598T Substitution - Missense 1:6121225-6121225 - TCGA-22-5472-01 COSM681589 c.2686G>T p.E896* Substitution - Nonsense 1:6136527-6136527 - PTC-7C COSM4144114 c.5052T>A p.G1684G Substitution - coding silent 1:6112228-6112228 - 2_PRE-TREATMENT COSM1721701 c.5736C>T p.I1912I Substitution - coding silent 1:6106622-6106622 - p1_II-1 COSM1738211 c.781G>C p.D261H Substitution - Missense 1:6152501-6152501 - LP6007398-DNA_A01 COSM5951667 c.3125G>A p.R1042H Substitution - Missense 1:6134147-6134147 - TCGA-EB-A5UL-06 COSM3491492 c.832T>A p.F278I Substitution - Missense 1:6152450-6152450 - ICGC_0006 COSM1158625 c.5319G>A p.K1773K Substitution - coding silent 1:6110457-6110457 - TCGA-CD-8536-01 COSM4009180 c.3491G>A p.R1164H Substitution - Missense 1:6128966-6128966 - SNU-175 COSM2237804 c.3407G>A p.R1136H Substitution - Missense 1:6129050-6129050 - TCGA-EI-6882-01 COSM1243159 c.5070C>T p.D1690D Substitution - coding silent 1:6112210-6112210 - TCGA-GF-A6C9-06 COSM3491505 c.120C>T p.F40F Substitution - coding silent 1:6168237-6168237 - TCGA-GM-A2D9-01 COSM3805676 c.5077A>G p.K1693E Substitution - Missense 1:6112203-6112203 - PASFXA COSM5005842 c.1935-8T>C p.? Unknown 1:6143939-6143939 - TCGA-DA-A1I0-06 COSM1686343 c.388-1G>A p.? Unknown 1:6155718-6155718 - CSCC-56-T COSM4566843 c.4894_4895CC>TT p.P1632L Substitution - Missense 1:6121122-6121123 - CSCC-47-T COSM4548664 c.4536G>A p.K1512K Substitution - coding silent 1:6124520-6124520 - LUAD-S00484 COSM342948 c.3560A>T p.Q1187L Substitution - Missense 1:6128897-6128897 - TCGA-HJ-7597-01 COSM4009189 c.1695C>T p.S565S Substitution - coding silent 1:6146319-6146319 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.522897;Hs.522898 1p36.31 610771

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.M1049R c.3146T>G 1 6191807 HC A C Synonymous p.G189G c.567T>G 1 6214898 RCCC - A Frameshift p.G805Wfs*23 c.2412dupT 1 6202212 LGG A G Missense p.I1885T c.5654T>C 1 6166764 CM A G Missense p.L158P c.473T>C 1 6215692 GBM A G Missense p.R667G c.1999A>G 1 6203927 BRCA A G Missense p.V537A c.1610T>C 1 6206464 UCEC - AT Frameshift p.L1324Cfs*78 c.3968_3969insAT 1 6186741 OV A T IntronicSNV . c.3262+62T>A 1 6191629 NSCLC A T Missense p.F36I c.106T>A 1 6228311 PRAD A T Missense p.L1768H c.5303T>A 1 6170533 RCCC C A Missense p.A1162S c.3484G>T 1 6189033 GBM C A Missense p.G490V c.1469G>T 1 6206846 HC C A Missense p.K567N c.1701G>T 1 6206373 LUSC C A Missense p.Q717H c.2151G>T 1 6202558 STAD C A Missense p.R1101L c.3302G>T 1 6190349 PRAD C A Missense p.R296S c.888G>T 1 6211198 UCEC C A Missense p.R581L c.1742G>T 1 6206332 LUAD C A Missense p.S1658I c.4973G>T 1 6172998 HNSC C A Missense p.V680L c.2038G>T 1 6203888 LUAD C A Nonsense p.E1388* c.4162G>T 1 6185835 LUAD C A Nonsense p.E1535* c.4603G>T 1 6184104 ESCA C A Nonsense p.E646* c.1936G>T 1 6203990 STAD C A Nonsense p.E896* c.2686G>T 1 6196587 LUSC C A SpliceAcceptorSNV . c.1935-1G>T 1 6203992 LUAD C A Synonymous p.L1028L c.3084G>T 1 6194248 LUAD C A Synonymous p.T732T c.2196G>T 1 6202513 LUAD C A Synonymous p.V537V c.1611G>T 1 6206463 LUAD CC AA Missense p.G1423F c.4267_4268delinsTT 1 6185286 LUAD CC TA Missense p.E1865K c.5592_5593delinsTA 1 6166825 CM CC TT Missense p.D1248N c.3741_3742delinsAA 1 6188267 CM C - Frameshift p.E1307Kfs*94 c.3919delG 1 6186791 UCEC C - Frameshift p.G563Afs*30 c.1688delG 1 6206386 LUSC C G Missense p.D371H c.1111G>C 1 6209356 HNSC C G Missense p.G288A c.863G>C 1 6212479 UCEC C G SpliceAcceptorSNV . c.4913-1G>C 1 6173059 BLCA C G Synonymous p.L872L c.2616G>C 1 6196657 LUAD C T Missense p.A1708T c.5122G>A 1 6172218 UCEC C T Missense p.A1836T c.5506G>A 1 6169927 LUSC C T Missense p.A942T c.2824G>A 1 6195336 UCEC C T Missense p.C1834Y c.5501G>A 1 6169932 LUSC C T Missense p.D1334N c.4000G>A 1 6186710 SCLC C T Missense p.D1546N c.4636G>A 1 6184071 CM C T Missense p.D1734N c.5200G>A 1 6171884 CM C T Missense p.D607N c.1819G>A 1 6204199 CM C T Missense p.D676N c.2026G>A 1 6203900 CM C T Missense p.E1199K c.3595G>A 1 6188922 CM C T Missense p.E1283K c.3847G>A 1 6188162 CM C T Missense p.E140K c.418G>A 1 6215747 BRCA C T Missense p.E295K c.883G>A 1 6211203 BRCA C T Missense p.E69K c.205G>A 1 6228212 CM C T Missense p.E765K c.2293G>A 1 6202331 CM C T Missense p.E79K c.235G>A 1 6219548 CM C T Missense p.G1090E c.3269G>A 1 6190382 CM C T Missense p.G1196S c.3586G>A 1 6188931 CM C T Missense p.G1730E c.5189G>A 1 6171895 CM C T Missense p.G557S c.1669G>A 1 6206405 CM C T Missense p.G559E c.1676G>A 1 6206398 CM C T Missense p.G606R c.1816G>A 1 6204202 CM C T Missense p.R1069Q c.3206G>A 1 6191747 STAD C T Missense p.R1414Q c.4241G>A 1 6185603 CM C T Missense p.R1457Q c.4370G>A 1 6185184 UCEC C T Missense p.R1601K c.4802G>A 1 6181275 CM C T Missense p.R584H c.1751G>A 1 6206323 BLCA C T Missense p.R966Q c.2897G>A 1 6194893 CM C T Missense p.V187I c.559G>A 1 6214906 BLCA C T Missense p.V45M c.133G>A 1 6228284 RCCC C T Missense p.V980I c.2938G>A 1 6194852 CM C T Nonsense p.W1743* c.5229G>A 1 6171855 GBM C T Nonsense p.W591* c.1772G>A 1 6206302 CM C T SpliceAcceptorSNV . c.388-1G>A 1 6215778 CM C T SpliceAcceptorSNV . c.80-1G>A 1 6228338 CM C T SpliceDonorSNV . c.3144+1G>A 1 6194187 CM C T Synonymous p.A1480A c.4440G>A 1 6184676 CM C T Synonymous p.A1480A c.4440G>A 1 6184676 STAD C T Synonymous p.D1874D c.5622C>T 1 6166796 PAAD C T Synonymous p.E1623E c.4869G>A 1 6181208 CM C T Synonymous p.G1522G c.4566G>A 1 6184141 CM C T Synonymous p.G1699G c.5097G>A 1 6172243 CM C T Synonymous p.G1730G c.5190G>A 1 6171894 CM C T Synonymous p.G1849G c.5547G>A 1 6169886 CM C T Synonymous p.G70G c.210G>A 1 6219573 BLCA C T Synonymous p.G750G c.2250G>A 1 6202374 CM C T Synonymous p.K1430K c.4290G>A 1 6185264 CM C T Synonymous p.K1773K c.5319G>A 1 6170517 PAAD C T Synonymous p.K1844K c.5532G>A 1 6169901 CM C T Synonymous p.K588K c.1764G>A 1 6206310 CM C T Synonymous p.L1590L c.4770G>A 1 6181563 CM C T Synonymous p.L370L c.1110G>A 1 6209357 CM C T Synonymous p.L503L c.1509G>A 1 6206806 BLCA C T Synonymous p.P1387P c.4161G>A 1 6185836 LUSC C T Synonymous p.P95P c.285G>A 1 6219498 CM C T Synonymous p.Q1139Q c.3417G>A 1 6189100 BLCA C T Synonymous p.Q1362Q c.4086G>A 1 6185911 CM C T Synonymous p.Q343Q c.1029G>A 1 6209438 GBM C T Synonymous p.Q351Q c.1053G>A 1 6209414 STAD C T Synonymous p.R1621R c.4863G>A 1 6181214 CM C T Synonymous p.R285R c.855G>A 1 6212487 CM C T Synonymous p.R645R c.1935G>A 1 6203991 CM C T Synonymous p.R65R c.195G>A 1 6228222 CM C T Synonymous p.R791R c.2373G>A 1 6202251 CM C T Synonymous p.R949R c.2847G>A 1 6195313 CM C T Synonymous p.S1545S c.4635G>A 1 6184072 BLCA C T Synonymous p.T781T c.2343G>A 1 6202281 CM C T Synonymous p.Y1733Y c.5199C>T 1 6171885 GBM G A IntronicSNV . c.3387+22C>T 1 6190242 CM G A Missense p.A772V c.2315C>T 1 6202309 BRCA G A Missense p.A909V c.2726C>T 1 6195434 GBM G A Missense p.D119N c.355G>A 1 6219428 BRCA G A Missense p.H1820Y c.5458C>T 1 6169975 BRCA G A Missense p.L708F c.2122C>T 1 6202587 LUSC G A Missense p.L739F c.2215C>T 1 6202494 SCLC G A Missense p.P1407L c.4220C>T 1 6185624 CM G A Missense p.P1632L c.4895C>T 1 6181182 GBM G A Missense p.P231L c.692C>T 1 6214773 LUAD G A Missense p.P502S c.1504C>T 1 6206811 CLL G A Missense p.R1136C c.3406C>T 1 6189111 STAD G A Missense p.R1147C c.3439C>T 1 6189078 BRCA G A Missense p.R1325W c.3973C>T 1 6186737 LGG G A Missense p.R1906C c.5716C>T 1 6166702 PRAD G A Missense p.R787C c.2359C>T 1 6202265 LUAD G A Missense p.S1018F c.3053C>T 1 6194279 CM G A Missense p.S1153L c.3458C>T 1 6189059 GBM G A Missense p.S1183F c.3548C>T 1 6188969 CM G A Missense p.S759F c.2276C>T 1 6202348 CM G A Missense p.T271M c.812C>T 1 6212530 COREAD G A Missense p.T536M c.1607C>T 1 6206467 ESCA G A Missense p.V45M c.133G>A 1 6228284 BRCA G A Nonsense p.Q166* c.496C>T 1 6215669 PRAD G A Synonymous p.A272A c.816C>T 1 6212526 RCCC G A Synonymous p.A364A c.1092C>T 1 6209375 BRCA G A Synonymous p.D1203D c.3609C>T 1 6188908 ESCA G A Synonymous p.D1203D c.3609C>T 1 6188908 LUAD G A Synonymous p.D1271D c.3813C>T 1 6188196 COREAD G A Synonymous p.D1445D c.4335C>T 1 6185219 ESCA G A Synonymous p.F1471F c.4413C>T 1 6184703 CM G A Synonymous p.F36F c.108C>T 1 6228309 HNSC G A Synonymous p.F40F c.120C>T 1 6228297 CM G A Synonymous p.F887F c.2661C>T 1 6196612 LUSC G A Synonymous p.F937F c.2811C>T 1 6195349 CM G A Synonymous p.F999F c.2997C>T 1 6194793 CM G A Synonymous p.G837G c.2511C>T 1 6196851 HNSC G A Synonymous p.G976G c.2928C>T 1 6194862 UCEC G A Synonymous p.H156H c.468C>T 1 6215697 LUAD G A Synonymous p.I1707I c.5121C>T 1 6172219 CM G A Synonymous p.L1651L c.4951C>T 1 6173020 LUAD G A Synonymous p.L447L c.1339C>T 1 6208958 LUAD G A Synonymous p.N1826N c.5478C>T 1 6169955 STAD G A Synonymous p.P573P c.1719C>T 1 6206355 CM G A Synonymous p.R766R c.2298C>T 1 6202326 BRCA G A Synonymous p.S94S c.282C>T 1 6219501 CM G A Synonymous p.S973S c.2919C>T 1 6194871 CM G A Synonymous p.V228V c.684C>T 1 6214781 CM G A Synonymous p.Y583Y c.1749C>T 1 6206325 BRCA G A Synonymous p.Y776Y c.2328C>T 1 6202296 UCEC GAT - InFrameDeletion p.I693delI c.2077_2079delATC 1 6202630 HNSC G C Missense p.L529V c.1585C>G 1 6206730 GBM G C Missense p.S1496C c.4487C>G 1 6184629 LUAD G C Synonymous p.L1200L c.3600C>G 1 6188917 BLCA G C Synonymous p.L823L c.2469C>G 1 6196893 BLCA G C Synonymous p.P1552P c.4656C>G 1 6184051 GBM G C Synonymous p.P996P c.2988C>G 1 6194802 THCA - G Frameshift p.L465Tfs*28 c.1391dupC 1 6206924 OV GG AA Missense p.P1242L c.3724_3725delinsTT 1 6188564 CM GG AA Missense p.P230L c.689_690delinsTT 1 6214775 CM GG AA Missense p.P553F c.1657_1658delinsTT 1 6206416 CM G T Missense p.D1580E c.4740C>A 1 6181593 BRCA G T Missense p.N176K c.528C>A 1 6214937 ESCA G T Missense p.N444K c.1332C>A 1 6208965 RCCC G T Missense p.P1387T c.4159C>A 1 6185838 LUAD G T Missense p.Q1840K c.5518C>A 1 6169915 LUAD G T Nonsense p.C992* c.2976C>A 1 6194814 LUAD G T Synonymous p.L889L c.2667C>A 1 6196606 LUAD T A Missense p.I1219F c.3655A>T 1 6188634 HNSC T A Missense p.K1031M c.3092A>T 1 6194240 LUAD T C Missense p.M1167V c.3499A>G 1 6189018 OV T C Missense p.M1881V c.5641A>G 1 6166777 SCLC T C Missense p.N1011D c.3031A>G 1 6194301 LUSC T C Missense p.N570D c.1708A>G 1 6206366 HC T C Missense p.Y1733C c.5198A>G 1 6171886 RCCC T C Missense p.Y1811C c.5432A>G 1 6170001 LUSC T G Missense p.N1683H c.5047A>C 1 6172293 GBM TTC - InFrameDeletion p.K102delK c.303_305delGAA 1 6219478 UCEC