Primary Site >> Liver Cancer
Gene >> ITGA4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397033 |
| Start | 181475189:181475189(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.457T>G |
| AA Mutation | p.Tyr153Asp(p.Y153D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397033 |
| Start | 181485897:181485897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1058C>T |
| AA Mutation | p.Ala353Val(p.A353V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397033 |
| Start | 181524193:181524193(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2192A>T |
| AA Mutation | p.Asp731Val(p.D731V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397033 |
| Start | 181493401:181493401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1230C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397033 |
| Start | 181458301:181458301(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772834562 |
| CDS Mutation | c.303C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397033 |
| Start | 181493386:181493386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754585299 |
| CDS Mutation | c.1215C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |