Primary Site >> Liver Cancer
Gene >> GDF2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000581492 |
| Start | 47325033:47325033(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.539A>G |
| AA Mutation | p.Asp180Gly(p.D180G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000581492 |
| Start | 47325603:47325603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1109C>T |
| AA Mutation | p.Pro370Leu(p.P370L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000581492 |
| Start | 47325644:47325644(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1150T>C |
| AA Mutation | p.Phe384Leu(p.F384L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000581492 |
| Start | 47322774:47322774(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.106A>G |
| AA Mutation | p.Asn36Asp(p.N36D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000581492 |
| Start | 47325365:47325365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201711410 |
| CDS Mutation | c.871G>T |
| AA Mutation | p.Gly291Cys(p.G291C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000581492 |
| Start | 47325406:47325406(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201627211 |
| CDS Mutation | c.912G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000581492 |
| Start | 47322992:47322992(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.324T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000581492 |
| Start | 47322875:47322875(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.207C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000581492 |
| Start | 47322812:47322812(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.144G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |