Primary Site >> Liver Cancer
Gene >> FLT4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261937 |
| Start | 180621202:180621202(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2071G>A |
| AA Mutation | p.Val691Met(p.V691M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261937 |
| Start | 180603295:180603295(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3989A>G |
| AA Mutation | p.Gln1330Arg(p.Q1330R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000261937 |
| Start | 180616367:180616367(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3219T>A |
| AA Mutation | p.Ser1073Arg(p.S1073R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261937 |
| Start | 180621556:180621556(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2006A>G |
| AA Mutation | p.Tyr669Cys(p.Y669C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000261937 |
| Start | 180616901:180616901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3095A>T |
| AA Mutation | p.Lys1032Met(p.K1032M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261937 |
| Start | 180618886:180618886(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2885C>A |
| AA Mutation | p.Ala962Asp(p.A962D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261937 |
| Start | 180621891:180621891(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1671C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261937 |
| Start | 180621894:180621894(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143634822 |
| CDS Mutation | c.1668C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |