Primary Site >> Liver Cancer
Gene >> MUC5AC
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000621226 |
| Start | 1165726:1165726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372695156 |
| CDS Mutation | c.1352C>T |
| AA Mutation | p.Thr451Met(p.T451M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000621226 |
| Start | 1167944:1167944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1454C>T |
| AA Mutation | p.Thr485Ile(p.T485I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000621226 |
| Start | 1169005:1169005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1849T>A |
| AA Mutation | p.Cys617Ser(p.C617S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000621226 |
| Start | 1160616:1160616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.78T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000621226 |
| Start | 1162074:1162074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.379G>T |
| AA Mutation | p.Glu127Ter(p.E127*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000621226 |
| Start | 1162648:1162648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.588+2T>G |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |