Primary Site >> Liver Cancer
Gene >> GALNT3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392701 |
| Start | 165770304:165770304(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763127846 |
| CDS Mutation | c.397T>G |
| AA Mutation | p.Leu133Val(p.L133V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392701 |
| Start | 165748786:165748786(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1897G>C |
| AA Mutation | p.Asp633His(p.D633H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392701 |
| Start | 165759476:165759476(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.933G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | splice_donor_variant;coding_sequence_variant;intron_variant |
| Transcription ID | ENST00000392701 |
| Start | 165754924:165754939(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1517_1524+8delCTGGATACGTGAGTAT |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |