Primary Site >> Stomach Cancer
Gene >> S1PR2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000590320 |
| Start | 10224263:10224263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773248254 |
| CDS Mutation | c.643G>A |
| AA Mutation | p.Val215Met(p.V215M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000590320 |
| Start | 10223962:10223962(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777226501 |
| CDS Mutation | c.944G>A |
| AA Mutation | p.Arg315Gln(p.R315Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000590320 |
| Start | 10224798:10224798(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.108C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000590320 |
| Start | 10224795:10224795(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781176630 |
| CDS Mutation | c.111G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000590320 |
| Start | 10224348:10224348(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199954220 |
| CDS Mutation | c.558C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000590320 |
| Start | 10224672:10224672(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757513633 |
| CDS Mutation | c.234C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000590320 |
| Start | 10224708:10224708(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.198G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000590320 |
| Start | 10223972:10223972(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.934delG |
| AA Mutation | p.Val312CysfsTer83(p.V312Cfs*83) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |