Primary Site >> Stomach Cancer
Gene >> PGC
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373025 |
| Start | 41743356:41743356(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.362C>T |
| AA Mutation | p.Ser121Phe(p.S121F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373025 |
| Start | 41739935:41739935(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.779G>A |
| AA Mutation | p.Gly260Asp(p.G260D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373025 |
| Start | 41737753:41737753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.991C>G |
| AA Mutation | p.Pro331Ala(p.P331A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373025 |
| Start | 41742327:41742327(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143935750 |
| CDS Mutation | c.610G>A |
| AA Mutation | p.Ala204Thr(p.A204T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373025 |
| Start | 41744715:41744715(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.153T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373025 |
| Start | 41742415:41742415(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs186012055 |
| CDS Mutation | c.522G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |