Primary Site >> Stomach Cancer
Gene >> SIRPA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356025 |
| Start | 1937389:1937389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1336G>A |
| AA Mutation | p.Glu446Lys(p.E446K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356025 |
| Start | 1934720:1934720(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1232A>G |
| AA Mutation | p.His411Arg(p.H411R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356025 |
| Start | 1921577:1921577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.619T>A |
| AA Mutation | p.Tyr207Asn(p.Y207N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356025 |
| Start | 1921412:1921412(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143335460 |
| CDS Mutation | c.454G>A |
| AA Mutation | p.Val152Met(p.V152M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356025 |
| Start | 1937528:1937528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1475C>A |
| AA Mutation | p.Ser492Tyr(p.S492Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356025 |
| Start | 1921497:1921497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.539T>G |
| AA Mutation | p.Ile180Ser(p.I180S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356025 |
| Start | 1921680:1921680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369093228 |
| CDS Mutation | c.722G>A |
| AA Mutation | p.Arg241His(p.R241H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356025 |
| Start | 1922440:1922440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.882C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356025 |
| Start | 1937433:1937433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143207818 |
| CDS Mutation | c.1380G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356025 |
| Start | 1921642:1921642(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376873084 |
| CDS Mutation | c.684C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |