Primary Site >> Stomach Cancer
Gene >> FOXF1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262426 |
| Start | 86511039:86511039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.470T>C |
| AA Mutation | p.Met157Thr(p.M157T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262426 |
| Start | 86511030:86511030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.461T>C |
| AA Mutation | p.Met154Thr(p.M154T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262426 |
| Start | 86511074:86511074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.505A>G |
| AA Mutation | p.Thr169Ala(p.T169A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262426 |
| Start | 86510876:86510876(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.307A>G |
| AA Mutation | p.Asn103Asp(p.N103D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262426 |
| Start | 86511101:86511101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.532G>A |
| AA Mutation | p.Gly178Ser(p.G178S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262426 |
| Start | 86510786:86510786(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.217G>A |
| AA Mutation | p.Glu73Lys(p.E73K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262426 |
| Start | 86511413:86511413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.844G>A |
| AA Mutation | p.Ala282Thr(p.A282T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262426 |
| Start | 86510858:86510858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.289C>T |
| AA Mutation | p.Arg97Cys(p.R97C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262426 |
| Start | 86511003:86511003(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.434G>A |
| AA Mutation | p.Arg145Gln(p.R145Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262426 |
| Start | 86510948:86510948(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.379G>A |
| AA Mutation | p.Ala127Thr(p.A127T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262426 |
| Start | 86511142:86511142(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765091590 |
| CDS Mutation | c.573C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262426 |
| Start | 86511109:86511109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769016003 |
| CDS Mutation | c.540G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |