Primary Site >> Stomach Cancer
Gene >> MBNL1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282486 |
| Start | 152415071:152415071(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.305T>C |
| AA Mutation | p.Leu102Pro(p.L102P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282486 |
| Start | 152445298:152445298(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.566A>G |
| AA Mutation | p.Gln189Arg(p.Q189R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282486 |
| Start | 152432868:152432868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.497C>A |
| AA Mutation | p.Pro166His(p.P166H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282486 |
| Start | 152445370:152445370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.638C>T |
| AA Mutation | p.Thr213Ile(p.T213I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282486 |
| Start | 152447689:152447689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748628776 |
| CDS Mutation | c.931G>A |
| AA Mutation | p.Ala311Thr(p.A311T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282486 |
| Start | 152300280:152300280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773981630 |
| CDS Mutation | c.87G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |