Primary Site >> Stomach Cancer
Gene >> MRC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17880656:17880656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2851T>G |
| AA Mutation | p.Phe951Val(p.F951V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17866756:17866756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1978T>G |
| AA Mutation | p.Phe660Val(p.F660V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17907629:17907629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4009G>A |
| AA Mutation | p.Ala1337Thr(p.A1337T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000569591 |
| Start | 17880527:17880527(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2722T>G |
| AA Mutation | p.Phe908Val(p.F908V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17823167:17823167(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.155A>G |
| AA Mutation | p.Asp52Gly(p.D52G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17866697:17866697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1919C>T |
| AA Mutation | p.Thr640Met(p.T640M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17885346:17885346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3058T>G |
| AA Mutation | p.Phe1020Val(p.F1020V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17849661:17849661(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1146A>C |
| AA Mutation | p.Lys382Asn(p.K382N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17863572:17863572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1673G>T |
| AA Mutation | p.Arg558Met(p.R558M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17809470:17809470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5G>A |
| AA Mutation | p.Arg2Lys(p.R2K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17827658:17827658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.580T>C |
| AA Mutation | p.Cys194Arg(p.C194R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17823225:17823225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.213T>G |
| AA Mutation | p.Phe71Leu(p.F71L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17849611:17849611(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1096T>A |
| AA Mutation | p.Trp366Arg(p.W366R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17823371:17823371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.359G>A |
| AA Mutation | p.Gly120Asp(p.G120D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17866664:17866664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1886C>A |
| AA Mutation | p.Ala629Glu(p.A629E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17898064:17898064(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3281T>C |
| AA Mutation | p.Ile1094Thr(p.I1094T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17833706:17833706(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.669C>A |
| AA Mutation | p.Asp223Glu(p.D223E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17870860:17870860(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2124C>G |
| AA Mutation | p.Ser708Arg(p.S708R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000569591 |
| Start | 17827542:17827542(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.464C>T |
| AA Mutation | p.Ala155Val(p.A155V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17809473:17809473(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8T>C |
| AA Mutation | p.Leu3Pro(p.L3P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17898138:17898138(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3355G>A |
| AA Mutation | p.Ala1119Thr(p.A1119T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17866732:17866732(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1954G>A |
| AA Mutation | p.Ala652Thr(p.A652T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000569591 |
| Start | 17849628:17849628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1113T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000569591 |
| Start | 17880601:17880601(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2796C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000569591 |
| Start | 17910408:17910408(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4314T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000569591 |
| Start | 17872113:17872113(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2331C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000569591 |
| Start | 17866603:17866603(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1829delG |
| AA Mutation | p.Gly610AlafsTer6(p.G610Afs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000569591 |
| Start | 17809488:17809488(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.27delT |
| AA Mutation | p.Phe9LeufsTer18(p.F9Lfs*18) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000569591 |
| Start | 17823319:17823319(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.311delA |
| AA Mutation | p.Asn104MetfsTer57(p.N104Mfs*57) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000569591 |
| Start | 17861393:17861393(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1530delA |
| AA Mutation | p.Lys510AsnfsTer8(p.K510Nfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000569591 |
| Start | 17898093:17898093(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3313delA |
| AA Mutation | p.Ser1105AlafsTer6(p.S1105Afs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000569591 |
| Start | 17875139:17875139(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2436T>G |
| AA Mutation | p.Tyr812Ter(p.Y812*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000569591 |
| Start | 17881100:17881100(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2899A>T |
| AA Mutation | p.Arg967Ter(p.R967*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000569591 |
| Start | 17861413:17861413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1545C>A |
| AA Mutation | p.Cys515Ter(p.C515*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000569591 |
| Start | 17853083:17853084(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1370dupA |
| AA Mutation | p.Asn457LysfsTer23(p.N457Kfs*23) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000569591 |
| Start | 17881101:17881102(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2906dupA |
| AA Mutation | p.Asn969LysfsTer22(p.N969Kfs*22) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |