Primary Site >> Stomach Cancer
Gene >> FKBP15
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000238256 |
| Start | 113183760:113183760(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199849054 |
| CDS Mutation | c.1802G>A |
| AA Mutation | p.Arg601Gln(p.R601Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000238256 |
| Start | 113170592:113170592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745366625 |
| CDS Mutation | c.2696G>A |
| AA Mutation | p.Arg899Gln(p.R899Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000238256 |
| Start | 113199855:113199855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771241869 |
| CDS Mutation | c.607G>A |
| AA Mutation | p.Ala203Thr(p.A203T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000238256 |
| Start | 113193539:113193539(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1018C>G |
| AA Mutation | p.Leu340Val(p.L340V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000238256 |
| Start | 113169595:113169595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3114A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000238256 |
| Start | 113174566:113174566(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2241A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000238256 |
| Start | 113187841:113187841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1335A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000238256 |
| Start | 113196953:113196953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.843G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000238256 |
| Start | 113182865:113182865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1815T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000238256 |
| Start | 113178722:113178722(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs774060142 |
| CDS Mutation | c.1994delA |
| AA Mutation | p.Lys665ArgfsTer9(p.K665Rfs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000238256 |
| Start | 113178721:113178722(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1994dupA |
| AA Mutation | p.Glu666GlyfsTer37(p.E666Gfs*37) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |