Primary Site >> Liver Cancer
Gene >> FLT1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282397 |
| Start | 28385004:28385004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1997A>T |
| AA Mutation | p.Asn666Ile(p.N666I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282397 |
| Start | 28389969:28389969(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1796C>G |
| AA Mutation | p.Thr599Arg(p.T599R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000282397 |
| Start | 28433953:28433953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.679A>T |
| AA Mutation | p.Asn227Tyr(p.N227Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282397 |
| Start | 28427804:28427804(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1224C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282397 |
| Start | 28466949:28466949(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.342T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282397 |
| Start | 28438305:28438305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs537466636 |
| CDS Mutation | c.429C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |