Primary Site >> Liver Cancer
Gene >> MAN2A1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261483 |
| Start | 109713706:109713706(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.322T>G |
| AA Mutation | p.Ser108Ala(p.S108A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261483 |
| Start | 109784800:109784800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1634A>G |
| AA Mutation | p.Asn545Ser(p.N545S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261483 |
| Start | 109842430:109842430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2669A>G |
| AA Mutation | p.Asn890Ser(p.N890S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261483 |
| Start | 109842332:109842332(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2571A>G |
| AA Mutation | p.Ile857Met(p.I857M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261483 |
| Start | 109845893:109845893(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2729T>G |
| AA Mutation | p.Leu910Trp(p.L910W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261483 |
| Start | 109755346:109755346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.725A>G |
| AA Mutation | p.Gln242Arg(p.Q242R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261483 |
| Start | 109770372:109770372(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1027G>T |
| AA Mutation | p.Asp343Tyr(p.D343Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261483 |
| Start | 109788943:109788943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1770T>G |
| AA Mutation | p.His590Gln(p.H590Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261483 |
| Start | 109729482:109729482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777987831 |
| CDS Mutation | c.676A>G |
| AA Mutation | p.Ile226Val(p.I226V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261483 |
| Start | 109690490:109690490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769889577 |
| CDS Mutation | c.73A>G |
| AA Mutation | p.Met25Val(p.M25V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |