Primary Site >> Stomach Cancer
Gene >> ST3GAL2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342907 |
| Start | 70398299:70398299(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776217838 |
| CDS Mutation | c.232G>A |
| AA Mutation | p.Asp78Asn(p.D78N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342907 |
| Start | 70398397:70398397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374278069 |
| CDS Mutation | c.134C>T |
| AA Mutation | p.Thr45Met(p.T45M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342907 |
| Start | 70398238:70398238(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.293C>T |
| AA Mutation | p.Thr98Ile(p.T98I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342907 |
| Start | 70388475:70388475(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.605C>A |
| AA Mutation | p.Pro202His(p.P202H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342907 |
| Start | 70395108:70395108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.407C>A |
| AA Mutation | p.Pro136His(p.P136H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342907 |
| Start | 70395042:70395042(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.473C>T |
| AA Mutation | p.Ser158Leu(p.S158L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342907 |
| Start | 70388469:70388469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.611G>T |
| AA Mutation | p.Ser204Ile(p.S204I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342907 |
| Start | 70395030:70395030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369604137 |
| CDS Mutation | c.485G>A |
| AA Mutation | p.Arg162Gln(p.R162Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000342907 |
| Start | 70388501:70388501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.579C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000342907 |
| Start | 70388474:70388474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.606T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000342907 |
| Start | 70398366:70398366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762496575 |
| CDS Mutation | c.165C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000342907 |
| Start | 70382847:70382847(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749327464 |
| CDS Mutation | c.837G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |