Primary Site >> Stomach Cancer
Gene >> MYOC
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000037502 |
| Start | 171652278:171652278(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.334G>A |
| AA Mutation | p.Glu112Lys(p.E112K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000037502 |
| Start | 171636215:171636215(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1225G>A |
| AA Mutation | p.Glu409Lys(p.E409K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000037502 |
| Start | 171652236:171652236(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200120115 |
| CDS Mutation | c.376C>T |
| AA Mutation | p.Arg126Trp(p.R126W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000037502 |
| Start | 171636097:171636097(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1343C>A |
| AA Mutation | p.Thr448Asn(p.T448N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000037502 |
| Start | 171652159:171652159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.453T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000037502 |
| Start | 171636609:171636609(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.831C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000037502 |
| Start | 171636561:171636561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369169139 |
| CDS Mutation | c.879G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000037502 |
| Start | 171636309:171636309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140112372 |
| CDS Mutation | c.1131G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |