Primary Site >> Stomach Cancer
Gene >> GPC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264039 |
| Start | 240459146:240459146(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146749086 |
| CDS Mutation | c.283G>A |
| AA Mutation | p.Val95Ile(p.V95I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264039 |
| Start | 240462371:240462371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs557977354 |
| CDS Mutation | c.506G>A |
| AA Mutation | p.Arg169His(p.R169H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264039 |
| Start | 240465194:240465194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1252G>A |
| AA Mutation | p.Gly418Arg(p.G418R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264039 |
| Start | 240466286:240466286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201724796 |
| CDS Mutation | c.1673G>A |
| AA Mutation | p.Arg558Gln(p.R558Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264039 |
| Start | 240462458:240462458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200136097 |
| CDS Mutation | c.593C>T |
| AA Mutation | p.Ala198Val(p.A198V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264039 |
| Start | 240462316:240462316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.451T>C |
| AA Mutation | p.Tyr151His(p.Y151H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264039 |
| Start | 240464636:240464636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs550678562 |
| CDS Mutation | c.904G>A |
| AA Mutation | p.Asp302Asn(p.D302N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264039 |
| Start | 240462270:240462270(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777362324 |
| CDS Mutation | c.405G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |