Primary Site >> Liver Cancer
Gene >> MMP12
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000571244 |
| Start | 102872950:102872950(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200973192 |
| CDS Mutation | c.265G>A |
| AA Mutation | p.Ala89Thr(p.A89T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000571244 |
| Start | 102867971:102867971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.724T>A |
| AA Mutation | p.Tyr242Asn(p.Y242N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000571244 |
| Start | 102871598:102871598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.621A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000571244 |
| Start | 102871901:102871901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.402C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000571244 |
| Start | 102866391:102866391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.969C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000571244 |
| Start | 102874854:102874855(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.83dupA |
| AA Mutation | p.Asn28LysfsTer2(p.N28Kfs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |