Primary Site >> Stomach Cancer
Gene >> MS4A15
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405633 |
| Start | 60775692:60775692(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.700G>A |
| AA Mutation | p.Ala234Thr(p.A234T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405633 |
| Start | 60773425:60773425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764559217 |
| CDS Mutation | c.439G>A |
| AA Mutation | p.Val147Ile(p.V147I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405633 |
| Start | 60775624:60775624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.632A>C |
| AA Mutation | p.Asn211Thr(p.N211T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405633 |
| Start | 60763917:60763917(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.184C>T |
| AA Mutation | p.Pro62Ser(p.P62S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000405633 |
| Start | 60763811:60763811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs575190018 |
| CDS Mutation | c.78G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000405633 |
| Start | 60763778:60763778(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780211813 |
| CDS Mutation | c.45G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |