Primary Site >> Stomach Cancer
Gene >> GPC5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377067 |
| Start | 91693357:91693357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.496T>G |
| AA Mutation | p.Phe166Val(p.F166V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377067 |
| Start | 91907970:91907970(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1314A>C |
| AA Mutation | p.Lys438Asn(p.K438N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377067 |
| Start | 91693454:91693454(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.593G>A |
| AA Mutation | p.Arg198His(p.R198H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377067 |
| Start | 91448838:91448838(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.241G>A |
| AA Mutation | p.Ala81Thr(p.A81T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377067 |
| Start | 91693637:91693637(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.776C>A |
| AA Mutation | p.Pro259Gln(p.P259Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377067 |
| Start | 91756397:91756397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1257G>T |
| AA Mutation | p.Trp419Cys(p.W419C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377067 |
| Start | 92144961:92144961(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1533A>C |
| AA Mutation | p.Glu511Asp(p.E511D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377067 |
| Start | 91693405:91693405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.544G>A |
| AA Mutation | p.Gly182Ser(p.G182S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377067 |
| Start | 91908049:91908049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1393G>C |
| AA Mutation | p.Val465Leu(p.V465L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377067 |
| Start | 91908024:91908024(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1368T>A |
| AA Mutation | p.Asn456Lys(p.N456K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377067 |
| Start | 92866321:92866321(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1601T>G |
| AA Mutation | p.Ile534Ser(p.I534S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377067 |
| Start | 91693796:91693796(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202020898 |
| CDS Mutation | c.935T>C |
| AA Mutation | p.Ile312Thr(p.I312T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377067 |
| Start | 91693498:91693498(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.637G>A |
| AA Mutation | p.Gly213Arg(p.G213R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377067 |
| Start | 91693457:91693457(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771309970 |
| CDS Mutation | c.596G>A |
| AA Mutation | p.Arg199Gln(p.R199Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377067 |
| Start | 91907947:91907947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs76285944 |
| CDS Mutation | c.1291C>T |
| AA Mutation | p.Arg431Cys(p.R431C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377067 |
| Start | 91907973:91907973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1317C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377067 |
| Start | 91399202:91399202(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.156G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377067 |
| Start | 91448909:91448909(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.312G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377067 |
| Start | 92866379:92866379(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761812897 |
| CDS Mutation | c.1659G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377067 |
| Start | 91693215:91693215(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.354A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377067 |
| Start | 91756361:91756361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1221T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377067 |
| Start | 91399145:91399145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.99T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377067 |
| Start | 91693656:91693656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749523673 |
| CDS Mutation | c.795G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |