Primary Site >> Stomach Cancer
Gene >> MMP12
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000571244 |
| Start | 102871809:102871809(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61730845 |
| CDS Mutation | c.494G>A |
| AA Mutation | p.Arg165His(p.R165H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000571244 |
| Start | 102867949:102867949(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201987840 |
| CDS Mutation | c.746G>A |
| AA Mutation | p.Arg249His(p.R249H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000571244 |
| Start | 102867982:102867982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.713C>A |
| AA Mutation | p.Pro238His(p.P238H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000571244 |
| Start | 102865842:102865842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1139T>A |
| AA Mutation | p.Ile380Asn(p.I380N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000571244 |
| Start | 102871848:102871848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.455T>A |
| AA Mutation | p.Ile152Asn(p.I152N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000571244 |
| Start | 102872929:102872929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs189745605 |
| CDS Mutation | c.286G>A |
| AA Mutation | p.Asp96Asn(p.D96N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000571244 |
| Start | 102872930:102872930(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782209734 |
| CDS Mutation | c.285C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000571244 |
| Start | 102867993:102867993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782505343 |
| CDS Mutation | c.702C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000571244 |
| Start | 102873058:102873058(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.157delA |
| AA Mutation | p.Met53Ter(p.M53*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000571244 |
| Start | 102872897:102872897(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs782219122 |
| CDS Mutation | c.318delG |
| AA Mutation | p.Val108TyrfsTer18(p.V108Yfs*18) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |