Primary Site >> Stomach Cancer
Gene >> FUT4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358752 |
| Start | 94544285:94544285(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.152C>G |
| AA Mutation | p.Ala51Gly(p.A51G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358752 |
| Start | 94545347:94545347(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1214C>T |
| AA Mutation | p.Ala405Val(p.A405V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358752 |
| Start | 94545042:94545042(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.909C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358752 |
| Start | 94545534:94545534(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1401C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358752 |
| Start | 94544952:94544952(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.819A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358752 |
| Start | 94544868:94544868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.735G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000358752 |
| Start | 94545194:94545195(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs773047836 |
| CDS Mutation | c.1061_1062delAG |
| AA Mutation | p.Gln354ArgfsTer195(p.Q354Rfs*195) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |