Primary Site >> Stomach Cancer
Gene >> FGF6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228837 |
| Start | 4445320:4445320(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762919183 |
| CDS Mutation | c.251G>A |
| AA Mutation | p.Arg84Gln(p.R84Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228837 |
| Start | 4445315:4445315(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780465055 |
| CDS Mutation | c.256C>T |
| AA Mutation | p.Arg86Trp(p.R86W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000228837 |
| Start | 4444134:4444134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140216440 |
| CDS Mutation | c.449C>T |
| AA Mutation | p.Thr150Met(p.T150M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228837 |
| Start | 4445321:4445321(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373061794 |
| CDS Mutation | c.250C>T |
| AA Mutation | p.Arg84Trp(p.R84W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228837 |
| Start | 4444168:4444168(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759669908 |
| CDS Mutation | c.415G>A |
| AA Mutation | p.Val139Ile(p.V139I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228837 |
| Start | 4445467:4445467(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.104T>C |
| AA Mutation | p.Val35Ala(p.V35A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000228837 |
| Start | 4445250:4445250(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775761160 |
| CDS Mutation | c.321C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |