Primary Site >> Liver Cancer
Gene >> ITGB5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296181 |
| Start | 124873450:124873450(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.152A>G |
| AA Mutation | p.Lys51Arg(p.K51R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000296181 |
| Start | 124841549:124841549(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.614A>C |
| AA Mutation | p.Tyr205Ser(p.Y205S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296181 |
| Start | 124821426:124821426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.829A>G |
| AA Mutation | p.Thr277Ala(p.T277A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296181 |
| Start | 124821470:124821470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.785A>C |
| AA Mutation | p.Lys262Thr(p.K262T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000296181 |
| Start | 124873531:124873531(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.71G>C |
| AA Mutation | p.Gly24Ala(p.G24A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296181 |
| Start | 124873450:124873450(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.152A>T |
| AA Mutation | p.Lys51Ile(p.K51I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000296181 |
| Start | 124821319:124821319(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs185706140 |
| CDS Mutation | c.936C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000296181 |
| Start | 124764428:124764428(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2267delA |
| AA Mutation | p.Lys756SerfsTer76(p.K756Sfs*76) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |