Primary Site >> Stomach Cancer
Gene >> SLC16A4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369779 |
| Start | 110382962:110382962(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.92A>G |
| AA Mutation | p.Asn31Ser(p.N31S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000369779 |
| Start | 110381652:110381652(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145736696 |
| CDS Mutation | c.364G>A |
| AA Mutation | p.Gly122Ser(p.G122S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369779 |
| Start | 110376992:110376992(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1200C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369779 |
| Start | 110382859:110382859(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.195C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369779 |
| Start | 110381671:110381671(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.345G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369779 |
| Start | 110378971:110378971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.912T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369779 |
| Start | 110379106:110379106(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767989454 |
| CDS Mutation | c.777T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369779 |
| Start | 110363805:110363805(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs760697175 |
| CDS Mutation | c.1425delT |
| AA Mutation | p.Phe475LeufsTer12(p.F475Lfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |