Primary Site >> Liver Cancer
Gene >> MAP1B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296755 |
| Start | 72195648:72195648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2293T>C |
| AA Mutation | p.Ser765Pro(p.S765P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296755 |
| Start | 72197494:72197494(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4139T>A |
| AA Mutation | p.Met1380Lys(p.M1380K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296755 |
| Start | 72198306:72198306(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4951C>A |
| AA Mutation | p.Gln1651Lys(p.Q1651K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296755 |
| Start | 72194070:72194070(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775351695 |
| CDS Mutation | c.715G>A |
| AA Mutation | p.Val239Ile(p.V239I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296755 |
| Start | 72198627:72198627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5272G>C |
| AA Mutation | p.Asp1758His(p.D1758H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296755 |
| Start | 72107634:72107634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.103A>C |
| AA Mutation | p.Ser35Arg(p.S35R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296755 |
| Start | 72205091:72205091(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7259T>A |
| AA Mutation | p.Leu2420Gln(p.L2420Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296755 |
| Start | 72115772:72115772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.259T>A |
| AA Mutation | p.Ser87Thr(p.S87T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296755 |
| Start | 72195997:72195997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2642A>T |
| AA Mutation | p.Glu881Val(p.E881V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296755 |
| Start | 72200305:72200305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6950A>T |
| AA Mutation | p.Asp2317Val(p.D2317V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000296755 |
| Start | 72195737:72195737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2382T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000296755 |
| Start | 72197363:72197363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771081682 |
| CDS Mutation | c.4008C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000296755 |
| Start | 72199022:72199022(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5667T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000296755 |
| Start | 72196506:72196506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3151A>T |
| AA Mutation | p.Lys1051Ter(p.K1051*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000296755 |
| Start | 72199296:72199296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5941A>T |
| AA Mutation | p.Arg1981Ter(p.R1981*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |