Primary Site >> Stomach Cancer
Gene >> ST3GAL6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394162 |
| Start | 98770902:98770902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.113G>C |
| AA Mutation | p.Arg38Pro(p.R38P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394162 |
| Start | 98791950:98791950(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.866C>A |
| AA Mutation | p.Pro289His(p.P289H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394162 |
| Start | 98788445:98788445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.738A>C |
| AA Mutation | p.Lys246Asn(p.K246N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394162 |
| Start | 98768457:98768457(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.17T>C |
| AA Mutation | p.Val6Ala(p.V6A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394162 |
| Start | 98791985:98791985(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.901A>T |
| AA Mutation | p.Met301Leu(p.M301L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394162 |
| Start | 98793678:98793678(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140152670 |
| CDS Mutation | c.913G>A |
| AA Mutation | p.Ala305Thr(p.A305T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394162 |
| Start | 98791885:98791885(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759540737 |
| CDS Mutation | c.801G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |