Primary Site >> Esophagus Cancer
Gene >> MMP16
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286614 |
| Start | 88327107:88327107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.100G>C |
| AA Mutation | p.Val34Leu(p.V34L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286614 |
| Start | 88186567:88186567(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.313G>A |
| AA Mutation | p.Asp105Asn(p.D105N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286614 |
| Start | 88056218:88056218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1283T>A |
| AA Mutation | p.Ile428Lys(p.I428K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286614 |
| Start | 88074671:88074671(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1156C>T |
| AA Mutation | p.Arg386Trp(p.R386W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286614 |
| Start | 88327184:88327184(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.23C>G |
| AA Mutation | p.Thr8Ser(p.T8S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286614 |
| Start | 88074727:88074727(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1100G>A |
| AA Mutation | p.Arg367Gln(p.R367Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286614 |
| Start | 88167932:88167932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753769443 |
| CDS Mutation | c.446G>A |
| AA Mutation | p.Arg149His(p.R149H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286614 |
| Start | 88327201:88327201(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |