Primary Site >> Stomach Cancer
Gene >> MBOAT7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000245615 |
| Start | 54178861:54178861(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748238566 |
| CDS Mutation | c.935G>A |
| AA Mutation | p.Arg312Gln(p.R312Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000245615 |
| Start | 54183560:54183560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.454A>G |
| AA Mutation | p.Thr152Ala(p.T152A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000245615 |
| Start | 54174339:54174339(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368420662 |
| CDS Mutation | c.1124C>T |
| AA Mutation | p.Ala375Val(p.A375V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000245615 |
| Start | 54174427:54174427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372242233 |
| CDS Mutation | c.1036G>A |
| AA Mutation | p.Ala346Thr(p.A346T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000245615 |
| Start | 54174119:54174119(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1344T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000245615 |
| Start | 54174086:54174086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1377C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000245615 |
| Start | 54174407:54174407(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764456266 |
| CDS Mutation | c.1056C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000245615 |
| Start | 54174316:54174316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760617583 |
| CDS Mutation | c.1147C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |