Primary Site >> Stomach Cancer
Gene >> ACOT7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377855 |
| Start | 6281281:6281281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760234992 |
| CDS Mutation | c.865G>A |
| AA Mutation | p.Val289Ile(p.V289I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377855 |
| Start | 6264649:6264649(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756883014 |
| CDS Mutation | c.1091G>A |
| AA Mutation | p.Arg364Gln(p.R364Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377855 |
| Start | 6327407:6327407(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746248748 |
| CDS Mutation | c.547C>T |
| AA Mutation | p.Arg183Trp(p.R183W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000377855 |
| Start | 6281103:6281103(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1043T>C |
| AA Mutation | p.Val348Ala(p.V348A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377855 |
| Start | 6339575:6339575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.306C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377855 |
| Start | 6349752:6349752(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376851666 |
| CDS Mutation | c.288C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377855 |
| Start | 6339506:6339506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201434397 |
| CDS Mutation | c.375C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |