Primary Site >> Liver Cancer
Gene >> ITGB4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75727449:75727449(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs569235037 |
| CDS Mutation | c.208G>A |
| AA Mutation | p.Ala70Thr(p.A70T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75731298:75731298(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762334700 |
| CDS Mutation | c.1145G>A |
| AA Mutation | p.Arg382Gln(p.R382Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75742648:75742648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2849T>A |
| AA Mutation | p.Ile950Asn(p.I950N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75742649:75742649(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2850C>G |
| AA Mutation | p.Ile950Met(p.I950M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75733678:75733678(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1643G>A |
| AA Mutation | p.Gly548Glu(p.G548E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000200181 |
| Start | 75742342:75742342(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2635C>A |
| AA Mutation | p.Gln879Lys(p.Q879K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75727260:75727260(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146966502 |
| CDS Mutation | c.145G>T |
| AA Mutation | p.Ala49Ser(p.A49S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75742729:75742729(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2930G>T |
| AA Mutation | p.Arg977Leu(p.R977L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |