Primary Site >> Stomach Cancer
Gene >> FUT6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286955 |
| Start | 5831631:5831631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375534466 |
| CDS Mutation | c.937G>A |
| AA Mutation | p.Ala313Thr(p.A313T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286955 |
| Start | 5831816:5831816(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.752A>G |
| AA Mutation | p.His251Arg(p.H251R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286955 |
| Start | 5832161:5832161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.407T>C |
| AA Mutation | p.Met136Thr(p.M136T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286955 |
| Start | 5832482:5832482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.86G>A |
| AA Mutation | p.Cys29Tyr(p.C29Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286955 |
| Start | 5831728:5831728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760949055 |
| CDS Mutation | c.840C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286955 |
| Start | 5832121:5832121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750684382 |
| CDS Mutation | c.447C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000286955 |
| Start | 5832397:5832397(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.171delC |
| AA Mutation | p.Ala58ProfsTer6(p.A58Pfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000286955 |
| Start | 5832332:5832333(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.235dupC |
| AA Mutation | p.Arg79ProfsTer11(p.R79Pfs*11) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |