Primary Site >> Stomach Cancer
Gene >> FKTN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000223528 |
| Start | 105607902:105607902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.731A>C |
| AA Mutation | p.His244Pro(p.H244P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000223528 |
| Start | 105575044:105575044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12C>G |
| AA Mutation | p.Ile4Met(p.I4M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000223528 |
| Start | 105607940:105607940(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.769G>T |
| AA Mutation | p.Ala257Ser(p.A257S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000223528 |
| Start | 105601148:105601148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.169G>A |
| AA Mutation | p.Ala57Thr(p.A57T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000223528 |
| Start | 105615351:105615351(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs137951613 |
| CDS Mutation | c.854C>T |
| AA Mutation | p.Ala285Val(p.A285V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000223528 |
| Start | 105635245:105635245(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1367A>G |
| AA Mutation | p.Glu456Gly(p.E456G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000223528 |
| Start | 105635126:105635126(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774804160 |
| CDS Mutation | c.1248C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000223528 |
| Start | 105635117:105635117(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1239T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000223528 |
| Start | 105604319:105604319(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.474C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000223528 |
| Start | 105619989:105619989(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs750176716 |
| CDS Mutation | c.1106delT |
| AA Mutation | p.Phe369SerfsTer37(p.F369Sfs*37) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000223528 |
| Start | 105620050:105620050(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1167delA |
| AA Mutation | p.Lys389AsnfsTer17(p.K389Nfs*17) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000223528 |
| Start | 105596658:105596658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774922597 |
| CDS Mutation | c.165+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |