Primary Site >> Stomach Cancer
Gene >> FGF18
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274625 |
| Start | 171456780:171456780(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371575721 |
| CDS Mutation | c.599G>A |
| AA Mutation | p.Arg200Gln(p.R200Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274625 |
| Start | 171436235:171436235(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745353337 |
| CDS Mutation | c.212G>A |
| AA Mutation | p.Arg71His(p.R71H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274625 |
| Start | 171436168:171436168(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.145C>T |
| AA Mutation | p.Arg49Cys(p.R49C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274625 |
| Start | 171436201:171436201(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756441926 |
| CDS Mutation | c.178C>T |
| AA Mutation | p.Arg60Trp(p.R60W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000274625 |
| Start | 171436104:171436104(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.81C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000274625 |
| Start | 171456658:171456658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768567377 |
| CDS Mutation | c.477G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000274625 |
| Start | 171456622:171456622(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148727482 |
| CDS Mutation | c.441C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |