Primary Site >> Liver Cancer
Gene >> KDR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263923 |
| Start | 55107852:55107852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1297G>T |
| AA Mutation | p.Asp433Tyr(p.D433Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263923 |
| Start | 55104858:55104858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1772T>G |
| AA Mutation | p.Leu591Arg(p.L591R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263923 |
| Start | 55098248:55098248(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2398G>C |
| AA Mutation | p.Gly800Arg(p.G800R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263923 |
| Start | 55107781:55107781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1368C>G |
| AA Mutation | p.Ile456Met(p.I456M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263923 |
| Start | 55110691:55110691(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1054G>T |
| AA Mutation | p.Ala352Ser(p.A352S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263923 |
| Start | 55080068:55080068(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3944A>G |
| AA Mutation | p.Asp1315Gly(p.D1315G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263923 |
| Start | 55089695:55089695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759365650 |
| CDS Mutation | c.3300C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |