Primary Site >> Esophagus Cancer
Gene >> MARK1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366917 |
| Start | 220661994:220661994(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2216T>G |
| AA Mutation | p.Leu739Trp(p.L739W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366917 |
| Start | 220652144:220652144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1730G>T |
| AA Mutation | p.Arg577Leu(p.R577L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366917 |
| Start | 220618490:220618490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761658090 |
| CDS Mutation | c.733G>A |
| AA Mutation | p.Val245Ile(p.V245I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366917 |
| Start | 220581089:220581089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.280A>C |
| AA Mutation | p.Thr94Pro(p.T94P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366917 |
| Start | 220618339:220618339(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.582G>A |
| AA Mutation | p.Met194Ile(p.M194I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366917 |
| Start | 220652136:220652136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1722A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |