Primary Site >> Stomach Cancer
Gene >> SLAMF1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302035 |
| Start | 160637217:160637217(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757926113 |
| CDS Mutation | c.389G>A |
| AA Mutation | p.Arg130His(p.R130H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302035 |
| Start | 160637431:160637431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.175A>G |
| AA Mutation | p.Ser59Gly(p.S59G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302035 |
| Start | 160634718:160634718(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766075769 |
| CDS Mutation | c.595G>A |
| AA Mutation | p.Gly199Ser(p.G199S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302035 |
| Start | 160637350:160637350(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.256G>A |
| AA Mutation | p.Ala86Thr(p.A86T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302035 |
| Start | 160612554:160612554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.891C>A |
| AA Mutation | p.Phe297Leu(p.F297L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302035 |
| Start | 160619819:160619819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201439748 |
| CDS Mutation | c.821A>G |
| AA Mutation | p.Glu274Gly(p.E274G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302035 |
| Start | 160637414:160637414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.192C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302035 |
| Start | 160634848:160634848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773729465 |
| CDS Mutation | c.465C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |