Primary Site >> Stomach Cancer
Gene >> ACOT8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217455 |
| Start | 45843550:45843550(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746146702 |
| CDS Mutation | c.818A>G |
| AA Mutation | p.Tyr273Cys(p.Y273C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217455 |
| Start | 45843542:45843542(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749132839 |
| CDS Mutation | c.826G>A |
| AA Mutation | p.Glu276Lys(p.E276K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217455 |
| Start | 45855243:45855243(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753837428 |
| CDS Mutation | c.178G>A |
| AA Mutation | p.Val60Met(p.V60M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217455 |
| Start | 45844342:45844342(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.567A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000217455 |
| Start | 45844326:45844326(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.583delC |
| AA Mutation | p.Leu195Ter(p.L195*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000217455 |
| Start | 45844281:45844281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758520030 |
| CDS Mutation | c.628C>T |
| AA Mutation | p.Arg210Ter(p.R210*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |