Primary Site >> Stomach Cancer
Gene >> FBP1
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000375326 |
| Start | 94605574:94605574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.708T>G |
| AA Mutation | p.Asp236Glu(p.D236E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375326 |
| Start | 94620425:94620425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201591116 |
| CDS Mutation | c.237C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375326 |
| Start | 94617813:94617813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771750403 |
| CDS Mutation | c.381C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000375326 |
| Start | 94606905:94606906(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.614dupA |
| AA Mutation | p.Lys206GlufsTer3(p.K206Efs*3) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000375326 |
| Start | 94603516:94603517(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.880_881dupGG |
| AA Mutation | p.Met295GlufsTer11(p.M295Efs*11) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000375326 |
| Start | 94617803:94617804(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.390dupT |
| AA Mutation | p.Val131CysfsTer11(p.V131Cfs*11) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000375326 |
| Start | 94606906:94606908(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.612_614delAAA |
| AA Mutation | p.Lys206del(p.K206del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |