Primary Site >> Stomach Cancer
Gene >> B4GALNT1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341156 |
| Start | 57631072:57631072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.398C>T |
| AA Mutation | p.Ala133Val(p.A133V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341156 |
| Start | 57628177:57628177(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1088C>T |
| AA Mutation | p.Ala363Val(p.A363V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341156 |
| Start | 57628760:57628760(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144725094 |
| CDS Mutation | c.955C>A |
| AA Mutation | p.Arg319Ser(p.R319S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341156 |
| Start | 57626835:57626835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759652761 |
| CDS Mutation | c.1511A>G |
| AA Mutation | p.Tyr504Cys(p.Y504C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341156 |
| Start | 57627723:57627723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1279C>A |
| AA Mutation | p.Pro427Thr(p.P427T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341156 |
| Start | 57630263:57630263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs546888005 |
| CDS Mutation | c.601G>C |
| AA Mutation | p.Glu201Gln(p.E201Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341156 |
| Start | 57628759:57628759(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745356128 |
| CDS Mutation | c.956G>A |
| AA Mutation | p.Arg319His(p.R319H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341156 |
| Start | 57630300:57630300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.564C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341156 |
| Start | 57628773:57628773(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs532276615 |
| CDS Mutation | c.942C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341156 |
| Start | 57627700:57627700(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778860816 |
| CDS Mutation | c.1302C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |