Primary Site >> Stomach Cancer
Gene >> ST8SIA4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231461 |
| Start | 100886518:100886518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.328T>C |
| AA Mutation | p.Tyr110His(p.Y110H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231461 |
| Start | 100811995:100811995(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769426294 |
| CDS Mutation | c.932C>T |
| AA Mutation | p.Ala311Val(p.A311V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231461 |
| Start | 100811972:100811972(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.955G>A |
| AA Mutation | p.Asp319Asn(p.D319N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231461 |
| Start | 100856209:100856209(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.691A>G |
| AA Mutation | p.Lys231Glu(p.K231E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231461 |
| Start | 100886469:100886469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.377G>T |
| AA Mutation | p.Ser126Ile(p.S126I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231461 |
| Start | 100856115:100856115(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.785A>G |
| AA Mutation | p.His262Arg(p.H262R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231461 |
| Start | 100902952:100902952(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4C>T |
| AA Mutation | p.Arg2Cys(p.R2C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231461 |
| Start | 100886502:100886502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376980451 |
| CDS Mutation | c.344G>A |
| AA Mutation | p.Arg115His(p.R115H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231461 |
| Start | 100812059:100812059(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.868A>G |
| AA Mutation | p.Arg290Gly(p.R290G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231461 |
| Start | 100856207:100856207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.693A>C |
| AA Mutation | p.Lys231Asn(p.K231N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231461 |
| Start | 100856373:100856373(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.527A>G |
| AA Mutation | p.Glu176Gly(p.E176G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231461 |
| Start | 100812116:100812116(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.811A>G |
| AA Mutation | p.Asn271Asp(p.N271D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000231461 |
| Start | 100886581:100886581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.265T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000231461 |
| Start | 100902854:100902854(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.102G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000231461 |
| Start | 100811994:100811994(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745413528 |
| CDS Mutation | c.933G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |