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 BLCA 6 30071549 30071549 + Missense_Mutation SNP C C T TCGA-FD-A3N5-01A-11D-A21A-08 TCGA-FD-A3N5-10A-01D-A21A-08 g.chr6:30071549C>T c.1042G>A c.(1042-1044)Ggg>Agg p.G348R BLCA 6 30071884 30071884 + Missense_Mutation SNP G G C TCGA-XF-AAN5-01A-11D-A42E-08 TCGA-XF-AAN5-10A-01D-A42H-08 g.chr6:30071884G>C c.1019C>G c.(1018-1020)tCt>tGt p.S340C BLCA 6 30080495 30080495 + Missense_Mutation SNP C C T TCGA-CU-A3YL-01A-11D-A22Z-08 TCGA-CU-A3YL-10A-01D-A22Z-08 g.chr6:30080495C>T c.88G>A c.(88-90)Gac>Aac p.D30N BLCA 6 30080562 30080562 + Silent SNP C C T TCGA-XF-A9T0-01A-11D-A391-08 TCGA-XF-A9T0-10A-01D-A394-08 g.chr6:30080562C>T c.21G>A c.(19-21)gtG>gtA p.V7V CESC 6 30071895 30071895 + Silent SNP G G A TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr6:30071895G>A c.1008C>T c.(1006-1008)ccC>ccT p.P336P CESC 6 30080457 30080457 + Missense_Mutation SNP C C G TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr6:30080457C>G c.126G>C c.(124-126)caG>caC p.Q42H COAD 6 30071565 30071565 + Splice_Site SNP G G A TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr6:30071565G>A c.1026C>T c.(1024-1026)ggC>ggT p.G342G COAD 6 30071892 30071892 + Silent SNP C C T TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr6:30071892C>T c.1011G>A c.(1009-1011)ggG>ggA p.G337G COAD 6 30078241 30078241 + Missense_Mutation SNP G G A TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr6:30078241G>A c.728C>T c.(727-729)cCc>cTc p.P243L COAD 6 30079476 30079478 + In_Frame_Del DEL CTT CTT - TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr6:30079476_30079478delCTT c.460_462delAAG c.(460-462)aagdel p.K154del COAD 6 30080533 30080533 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr6:30080533G>A c.50C>T c.(49-51)cCc>cTc p.P17L COADREAD 6 30071565 30071565 + Splice_Site SNP G G A TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr6:30071565G>A c.1026C>T c.(1024-1026)ggC>ggT p.G342G COADREAD 6 30071892 30071892 + Silent SNP C C T TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr6:30071892C>T c.1011G>A c.(1009-1011)ggG>ggA p.G337G COADREAD 6 30078241 30078241 + Missense_Mutation SNP G G A TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr6:30078241G>A c.728C>T c.(727-729)cCc>cTc p.P243L COADREAD 6 30078241 30078241 + Missense_Mutation SNP G G A TCGA-F5-6811-01A-11D-1826-10 TCGA-F5-6811-10A-01D-1826-10 g.chr6:30078241G>A c.728C>T c.(727-729)cCc>cTc p.P243L COADREAD 6 30079476 30079478 + In_Frame_Del DEL CTT CTT - TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr6:30079476_30079478delCTT c.460_462delAAG c.(460-462)aagdel p.K154del COADREAD 6 30080533 30080533 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr6:30080533G>A c.50C>T c.(49-51)cCc>cTc p.P17L ESCA 6 30071921 30071921 + Missense_Mutation SNP G G A TCGA-Q9-A6FW-01A-31D-A31U-09 TCGA-Q9-A6FW-10A-01D-A31U-09 g.chr6:30071921G>A c.982C>T c.(982-984)Cat>Tat p.H328Y ESCA 6 30080455 30080455 + Missense_Mutation SNP A A G TCGA-L5-A8NV-01A-11D-A37C-09 TCGA-L5-A8NV-11A-11D-A37F-09 g.chr6:30080455A>G c.128T>C c.(127-129)aTt>aCt p.I43T HNSC 6 30076801 30076801 + Splice_Site SNP A A G TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr6:30076801A>G c.e5+1 KIPAN 6 30072974 30072974 + Missense_Mutation SNP T T A TCGA-MH-A856-01A-11D-A34Z-10 TCGA-MH-A856-10A-01D-A34Z-10 g.chr6:30072974T>A c.929A>T c.(928-930)aAa>aTa p.K310I KIRP 6 30072974 30072974 + Missense_Mutation SNP T T A TCGA-MH-A856-01A-11D-A34Z-10 TCGA-MH-A856-10A-01D-A34Z-10 g.chr6:30072974T>A c.929A>T c.(928-930)aAa>aTa p.K310I LIHC 6 30075888 30075888 + Frame_Shift_Del DEL T T - TCGA-DD-A1EG-01A-11D-A20W-10 TCGA-DD-A1EG-10A-01D-A20W-10 g.chr6:30075888delT c.825delA c.(823-825)aaafs p.K275fs LIHC 6 30080321 30080321 + Missense_Mutation SNP A A G TCGA-RC-A6M4-01A-11D-A32G-10 TCGA-RC-A6M4-10A-01D-A32G-10 g.chr6:30080321A>G c.262T>C c.(262-264)Tcc>Ccc p.S88P LUAD 6 30071355 30071355 + Silent SNP C C T TCGA-69-7980-01A-11D-2184-08 TCGA-69-7980-10A-01D-2184-08 g.chr6:30071355C>T c.1236G>A c.(1234-1236)ctG>ctA p.L412L LUAD 6 30071450 30071450 + Missense_Mutation SNP C C T TCGA-44-7660-01A-11D-2063-08 TCGA-44-7660-10A-01D-2063-08 g.chr6:30071450C>T c.1141G>A c.(1141-1143)Gat>Aat p.D381N LUAD 6 30072985 30072985 + Missense_Mutation SNP G G C TCGA-05-4250-01A-01D-1105-08 TCGA-05-4250-10A-01D-1105-08 g.chr6:30072985G>C c.918C>G c.(916-918)aaC>aaG p.N306K LUAD 6 30078327 30078327 + Silent SNP C C T TCGA-55-7727-01A-11D-2167-08 TCGA-55-7727-10A-01D-2167-08 g.chr6:30078327C>T c.642G>A c.(640-642)ggG>ggA p.G214G LUAD 6 30080255 30080255 + Missense_Mutation SNP C C T TCGA-86-8073-01A-11D-2238-08 TCGA-86-8073-10A-01D-2238-08 g.chr6:30080255C>T c.328G>A c.(328-330)Ggg>Agg p.G110R OV 6 30071439 30071439 + Silent SNP A A G TCGA-29-1775-01A-01W-0639-09 TCGA-29-1775-10A-01W-0639-09 g.chr6:30071439A>G c.1152T>C c.(1150-1152)tcT>tcC p.S384S OV 6 30080570 30080570 + Missense_Mutation SNP G G T TCGA-13-0793-01A-01W-0370-10 TCGA-13-0793-10A-01W-0370-10 g.chr6:30080570G>T c.13C>A c.(13-15)Cag>Aag p.Q5K PRAD 6 30071498 30071498 + Missense_Mutation SNP A A C TCGA-EJ-7783-01A-11D-2114-08 TCGA-EJ-7783-10A-01D-2114-08 g.chr6:30071498A>C c.1093T>G c.(1093-1095)Tcg>Gcg p.S365A PRAD 6 30078314 30078314 + Missense_Mutation SNP C C T TCGA-HC-7213-01A-11D-2114-08 TCGA-HC-7213-10A-01D-2115-08 g.chr6:30078314C>T c.655G>A c.(655-657)Gcc>Acc p.A219T PRAD 6 30080303 30080303 + Missense_Mutation SNP T T C TCGA-V1-A8MM-01A-11D-A377-08 TCGA-V1-A8MM-10A-01D-A37A-08 g.chr6:30080303T>C c.280A>G c.(280-282)Aca>Gca p.T94A READ 6 30078241 30078241 + Missense_Mutation SNP G G A TCGA-F5-6811-01A-11D-1826-10 TCGA-F5-6811-10A-01D-1826-10 g.chr6:30078241G>A c.728C>T c.(727-729)cCc>cTc p.P243L SARC 6 30078449 30078449 + Missense_Mutation SNP C C T TCGA-IE-A3OV-01A-11D-A228-09 TCGA-IE-A3OV-11A-22D-A22A-09 g.chr6:30078449C>T c.520G>A c.(520-522)Gta>Ata p.V174I SKCM 6 30071529 30071529 + Silent SNP A A T TCGA-ER-A19D-06A-11D-A197-08 TCGA-ER-A19D-10A-01D-A199-08 g.chr6:30071529A>T c.1062T>A c.(1060-1062)tcT>tcA p.S354S SKCM 6 30071943 30071943 + Splice_Site SNP C C T TCGA-EE-A2M6-06A-12D-A197-08 TCGA-EE-A2M6-10A-01D-A199-08 g.chr6:30071943C>T c.960G>A c.(958-960)tgG>tgA p.W320* SKCM 6 30075851 30075851 + Missense_Mutation SNP C C T TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr6:30075851C>T c.862G>A c.(862-864)Ggg>Agg p.G288R SKCM 6 30075858 30075858 + Silent SNP G G A TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr6:30075858G>A c.855C>T c.(853-855)tcC>tcT p.S285S SKCM 6 30075913 30075913 + Missense_Mutation SNP G G A TCGA-D3-A3C8-06A-12D-A19A-08 TCGA-D3-A3C8-10A-01D-A19A-08 g.chr6:30075913G>A c.800C>T c.(799-801)cCt>cTt p.P267L SKCM 6 30075932 30075932 + Missense_Mutation SNP G G T TCGA-FR-A44A-06A-11D-A24R-08 TCGA-FR-A44A-10A-01D-A24R-08 g.chr6:30075932G>T c.781C>A c.(781-783)Cag>Aag p.Q261K SKCM 6 30076814 30076814 + Silent SNP G G A TCGA-EE-A2MD-06A-11D-A197-08 TCGA-EE-A2MD-10A-01D-A199-08 g.chr6:30076814G>A c.756C>T c.(754-756)gtC>gtT p.V252V SKCM 6 30078327 30078327 + Silent SNP C C T TCGA-D3-A51T-06A-11D-A25O-08 TCGA-D3-A51T-10A-01D-A25O-08 g.chr6:30078327C>T c.642G>A c.(640-642)ggG>ggA p.G214G SKCM 6 30078327 30078327 + Silent SNP C C T TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr6:30078327C>T c.642G>A c.(640-642)ggG>ggA p.G214G SKCM 6 30079499 30079499 + Nonsense_Mutation SNP G G A TCGA-DA-A1I1-06A-12D-A196-08 TCGA-DA-A1I1-10A-01D-A198-08 g.chr6:30079499G>A c.439C>T c.(439-441)Caa>Taa p.Q147* SKCM 6 30079500 30079500 + Silent SNP G G A TCGA-EE-A2MK-06A-11D-A196-08 TCGA-EE-A2MK-10A-01D-A198-08 g.chr6:30079500G>A c.438C>T c.(436-438)atC>atT p.I146I SKCM 6 30080208 30080208 + Silent SNP G G A TCGA-EE-A29S-06A-11D-A197-08 TCGA-EE-A29S-10A-01D-A199-08 g.chr6:30080208G>A c.375C>T c.(373-375)tcC>tcT p.S125S SKCM 6 30080278 30080278 + Missense_Mutation SNP A A T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr6:30080278A>T c.305T>A c.(304-306)tTc>tAc p.F102Y SKCM 6 30080296 30080296 + Missense_Mutation SNP G G A TCGA-D3-A51F-06A-11D-A25O-08 TCGA-D3-A51F-10A-01D-A25O-08 g.chr6:30080296G>A c.287C>T c.(286-288)cCg>cTg p.P96L SKCM 6 30080314 30080314 + Missense_Mutation SNP C C T TCGA-FS-A1ZK-06A-11D-A197-08 TCGA-FS-A1ZK-10A-01D-A199-08 g.chr6:30080314C>T c.269G>A c.(268-270)aGg>aAg p.R90K

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand HCC135T COSM3662344 c.487G>A p.G163S Substitution - Missense 6:30111674-30111674 - TCGA-HU-8602-01 COSM3861357 c.12G>A p.G4G Substitution - coding silent 6:30112794-30112794 - HCC2998 COSM3250999 c.610T>G p.Y204D Substitution - Missense 6:30110582-30110582 - TCGA-D3-A3C8-06 COSM3624132 c.800C>T p.P267L Substitution - Missense 6:30108136-30108136 - TCGA-AM-5821-01 COSM3761789 c.810G>A p.L270L Substitution - coding silent 6:30108126-30108126 - HCC135 COSM3662344 c.487G>A p.G163S Substitution - Missense 6:30111674-30111674 - TCGA-AA-3525-01 COSM291758 c.460_462delAAG p.K154delK Deletion - In frame 6:30111699-30111701 - ESCC_BICR_036T COSM5432216 c.850G>T p.D284Y Substitution - Missense 6:30108086-30108086 - TCGA-EE-A2MK-06 COSM3624137 c.438C>T p.I146I Substitution - coding silent 6:30111723-30111723 - TCGA-FS-A1ZZ-06 COSM3624131 c.855C>T p.S285S Substitution - coding silent 6:30108081-30108081 - sysucc-882T COSM5447695 c.114A>C p.K38N Substitution - Missense 6:30112692-30112692 - TCGA-ER-A19D-06 COSM3624128 c.1062T>A p.S354S Substitution - coding silent 6:30103752-30103752 - TCGA-BR-4184-01 COSM3861356 c.177C>T p.S59S Substitution - coding silent 6:30112629-30112629 - TCGA-CU-A3YL-01 COSM3777435 c.88G>A p.D30N Substitution - Missense 6:30112718-30112718 - TCGA-EJ-5527-01 COSM1131938 c.178G>A p.V60I Substitution - Missense 6:30112628-30112628 - TCGA-AX-A0J1-01 COSM1077302 c.564G>A p.L188L Substitution - coding silent 6:30110628-30110628 - TCGA-BS-A0UJ-01 COSM1077304 c.454A>C p.K152Q Substitution - Missense 6:30111707-30111707 - RKO COSM4614963 c.876delA p.K292fs*21 Deletion - Frameshift 6:30108060-30108060 - TCGA-D3-A51T-06 COSM1546071 c.642G>A p.G214G Substitution - coding silent 6:30110550-30110550 - TCGA-HU-A4GQ-01 COSM3861355 c.193A>C p.I65L Substitution - Missense 6:30112613-30112613 - CSCC-60-T COSM4539616 c.270G>A p.R90R Substitution - coding silent 6:30112536-30112536 - TCGA-EE-A2MS-06 COSM3624130 c.862G>A p.G288R Substitution - Missense 6:30108074-30108074 - T3152 COSM4736031 c.598C>A p.L200I Substitution - Missense 6:30110594-30110594 - PD3179a COSM1658905 c.1204G>A p.E402K Substitution - Missense 6:30103610-30103610 - S00827 COSM316139 c.30G>A p.L10L Substitution - coding silent 6:30112776-30112776 - HCC12 COSM1621375 c.853T>G p.S285A Substitution - Missense 6:30108083-30108083 - TCGA-D1-A17H-01 COSM1077301 c.726A>G p.P242P Substitution - coding silent 6:30110466-30110466 - OV203PT COSM253294 c.1238C>T p.T413I Substitution - Missense 6:30103576-30103576 - sysucc-274T COSM5476672 c.521T>C p.V174A Substitution - Missense 6:30110671-30110671 - B66-Tumor COSM4006269 c.193A>G p.I65V Substitution - Missense 6:30112613-30112613 - TCGA-JW-A5VL-01 COSM4847615 c.1008C>T p.P336P Substitution - coding silent 6:30104118-30104118 - DLD1 COSM3251001 c.520G>A p.V174I Substitution - Missense 6:30110672-30110672 - TCGA-DA-A1I1-06 COSM3624136 c.439C>T p.Q147* Substitution - Nonsense 6:30111722-30111722 - T3056 COSM4736032 c.574C>T p.L192L Substitution - coding silent 6:30110618-30110618 - TCGA-DD-A113-01 COSM4925376 c.1254G>T p.W418C Substitution - Missense 6:30103560-30103560 - HCT15 COSM3251001 c.520G>A p.V174I Substitution - Missense 6:30110672-30110672 - TCGA-A3-3374-01 COSM1496312 c.1100C>A p.A367D Substitution - Missense 6:30103714-30103714 - TCGA-HC-7213-01 COSM1471885 c.655G>A p.A219T Substitution - Missense 6:30110537-30110537 - TCGA-EE-A2MR-06 COSM3624139 c.305T>A p.F102Y Substitution - Missense 6:30112501-30112501 - TCGA-13-0793-01 COSM116632 c.13C>A p.Q5K Substitution - Missense 6:30112793-30112793 - NB-1480 COSM1288619 c.31C>A p.Q11K Substitution - Missense 6:30112775-30112775 - TCGA-A5-A0GP-01 COSM1077305 c.301A>C p.M101L Substitution - Missense 6:30112505-30112505 - S00827 COSM316139 c.30G>A p.L10L Substitution - coding silent 6:30112776-30112776 - TCGA-AZ-4315-01 COSM1442969 c.50C>T p.P17L Substitution - Missense 6:30112756-30112756 - TCGA-CK-6746-01 COSM1442967 c.1011G>A p.G337G Substitution - coding silent 6:30104115-30104115 - CSCC-27-T COSM4544824 c.364G>A p.D122N Substitution - Missense 6:30112442-30112442 - ME009T COSM223067 c.637G>A p.A213T Substitution - Missense 6:30110555-30110555 - TCGA-AA-3952-01 COSM5115959 c.254A>C p.E85A Substitution - Missense 6:30112552-30112552 - TCGA-AZ-6601-01 COSM5142796 c.1163C>T p.A388V Substitution - Missense 6:30103651-30103651 - TCGA-AA-3672-01 COSM267637 c.1026C>T p.G342G Substitution - coding silent 6:30103788-30103788 - C086 COSM5540807 c.1212C>T p.L404L Substitution - coding silent 6:30103602-30103602 - TCGA-G9-6496-01 COSM1131939 c.849T>C p.H283H Substitution - coding silent 6:30108087-30108087 - TCGA-EE-A29S-06 COSM3624138 c.375C>T p.S125S Substitution - coding silent 6:30112431-30112431 - TCGA-EB-A3Y7-01 COSM3921296 c.98A>C p.H33P Substitution - Missense 6:30112708-30112708 - LAU165 COSM235509 c.903G>A p.R301R Substitution - coding silent 6:30105223-30105223 - TCGA-29-1775-01 COSM1329118 c.1152T>C p.S384S Substitution - coding silent 6:30103662-30103662 - SNUH_G76_S1 COSM4416298 c.352C>T p.R118C Substitution - Missense 6:30112454-30112454 - TCGA-CG-5721-01 COSM3861354 c.723G>A p.M241I Substitution - Missense 6:30110469-30110469 - TCGA-D1-A103-01 COSM1077300 c.740T>G p.L247R Substitution - Missense 6:30110452-30110452 - RK225_C01 COSM4944780 c.1037C>T p.T346I Substitution - Missense 6:30103777-30103777 - TCGA-EE-A2MD-06 COSM3624134 c.756C>T p.V252V Substitution - coding silent 6:30109037-30109037 - PD7299a COSM1638163 c.435G>A p.Q145Q Substitution - coding silent 6:30111726-30111726 - PT25 COSM1131938 c.178G>A p.V60I Substitution - Missense 6:30112628-30112628 - 417 COSM4431746 c.307C>T p.H103Y Substitution - Missense 6:30112499-30112499 - PD11388a COSM5779758 c.1147A>T p.I383F Substitution - Missense 6:30103667-30103667 - ESCC_157 COSM5646434 c.789C>G p.L263L Substitution - coding silent 6:30108147-30108147 - LUAD-LIP77 COSM342534 c.638C>T p.A213V Substitution - Missense 6:30110554-30110554 - T2269 COSM4736029 c.1190A>G p.D397G Substitution - Missense 6:30103624-30103624 - TCGA-EE-A2M6-06 COSM3624129 c.960G>A p.W320* Substitution - Nonsense 6:30104166-30104166 - CSCC-56-T COSM235509 c.903G>A p.R301R Substitution - coding silent 6:30105223-30105223 - MO_1012 COSM5573170 c.768-2A>G p.? Unknown 6:30108170-30108170 - TCGA-AP-A056-01 COSM1077306 c.300G>A p.E100E Substitution - coding silent 6:30112506-30112506 - TCGA-EE-A2MJ-06 COSM1546071 c.642G>A p.G214G Substitution - coding silent 6:30110550-30110550 - TCGA-FS-A1ZK-06 COSM3624140 c.269G>A p.R90K Substitution - Missense 6:30112537-30112537 - BD6T COSM5498930 c.588_590delGAA p.K196delK Deletion - In frame 6:30110602-30110604 - CSCC-29-T COSM4547472 c.423G>A p.Q141Q Substitution - coding silent 6:30111738-30111738 - TCGA-WS-AB45-01 COSM5191479 c.134A>G p.E45G Substitution - Missense 6:30112672-30112672 - 4760_CLM COSM5756824 c.958T>C p.W320R Substitution - Missense 6:30105168-30105168 - S00827 COSM316138 c.31delC p.Q11fs*4 Deletion - Frameshift 6:30112775-30112775 - TCGA-Q1-A73O-01 COSM4836037 c.126G>C p.Q42H Substitution - Missense 6:30112680-30112680 - S00827 COSM316138 c.31delC p.Q11fs*4 Deletion - Frameshift 6:30112775-30112775 - LC_S9 COSM1191031 c.869_870insG p.F293fs*8 Insertion - Frameshift 6:30108066-30108067 - LB647-SCLC COSM24033 c.729C>T p.P243P Substitution - coding silent 6:30110463-30110463 - TCGA-EB-A41A-01 COSM3624135 c.742G>A p.E248K Substitution - Missense 6:30110450-30110450 - TCGA-EJ-7783-01 COSM1471886 c.1093T>G p.S365A Substitution - Missense 6:30103721-30103721 - CSCC-49-T COSM4469962 c.162C>T p.P54P Substitution - coding silent 6:30112644-30112644 - T2197 COSM4736030 c.616C>T p.L206L Substitution - coding silent 6:30110576-30110576 - TCGA-AM-5821-01 COSM3761788 c.1261G>A p.E421K Substitution - Missense 6:30103553-30103553 - ESCC_BICR_024T COSM5440959 c.251C>T p.S84F Substitution - Missense 6:30112555-30112555 - TCGA-AP-A051-01 COSM1077303 c.539G>T p.R180M Substitution - Missense 6:30110653-30110653 - HCC12T COSM1621375 c.853T>G p.S285A Substitution - Missense 6:30108083-30108083 - 970010 COSM1582676 c.992A>T p.N331I Substitution - Missense 6:30104134-30104134 - TCGA-FD-A3N5-01 COSM1311946 c.1042G>A p.G348R Substitution - Missense 6:30103772-30103772 - MD-285 COSM303447 c.1118C>T p.P373L Substitution - Missense 6:30103696-30103696 - TCGA-FR-A44A-06 COSM3624133 c.781C>A p.Q261K Substitution - Missense 6:30108155-30108155 - ccRCC-96 COSM1664681 c.791A>G p.N264S Substitution - Missense 6:30108145-30108145 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.493239;Hs.493240;Hs.493275 6p21.3 609316

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.S365A c.1093T>G 6 30071498 PRAD A T Synonymous p.S354S c.1062T>A 6 30071529 CM C T IntronicSNV . c.417+207G>A 6 30079959 CM C T IntronicSNV . c.513+30G>A 6 30079395 CM C T Missense p.A213T c.637G>A 6 30078332 CM C T Missense p.G288R c.862G>A 6 30075851 CM C T Missense p.G348R c.1042G>A 6 30071549 BLCA C T Missense p.R90K c.269G>A 6 30080314 CM C T Missense p.S311N c.932G>A 6 30072971 CM C T Missense p.V60I c.178G>A 6 30080405 PRAD C T Nonsense p.W320* c.960G>A 6 30071943 CM C T Synonymous p.G214G c.642G>A 6 30078327 CM C T Synonymous p.L10L c.30G>A 6 30080553 SCLC G A IntronicSNV . c.767+68C>T 6 30076735 CM G A IntronicSNV . c.768-8C>T 6 30075953 CM G A Missense p.P267L c.800C>T 6 30075913 CM G A Nonsense p.Q147* c.439C>T 6 30079499 CM G A Synonymous p.F170F c.510C>T 6 30079428 CM G A Synonymous p.I146I c.438C>T 6 30079500 CM G A Synonymous p.S285S c.855C>T 6 30075858 CM G A Synonymous p.V252V c.756C>T 6 30076814 CM G C Missense p.N306K c.918C>G 6 30072985 LUAD G - Frameshift p.Q11Kfs*4 c.31delC 6 30080552 SCLC G T Missense p.L235M c.703C>A 6 30078266 STAD G T Missense p.Q11K c.31C>A 6 30080552 NB G T Missense p.Q5K c.13C>A 6 30080570 OV T A Missense p.E278V c.833A>T 6 30075880 CM T C IntronicSNV . c.884-45A>G 6 30073064 CM T G Missense p.M101L c.301A>C 6 30080282 UCEC T G Synonymous p.P265P c.795A>C 6 30075918 CM