Primary Site >> Stomach Cancer
Gene >> FNBP1
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000446176 |
| Start | 129925156:129925156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.791A>T |
| AA Mutation | p.Asp264Val(p.D264V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000446176 |
| Start | 129908989:129908989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757294604 |
| CDS Mutation | c.1196C>T |
| AA Mutation | p.Pro399Leu(p.P399L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000446176 |
| Start | 129979318:129979318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.197A>C |
| AA Mutation | p.Lys66Thr(p.K66T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000446176 |
| Start | 129895943:129895943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1741G>A |
| AA Mutation | p.Glu581Lys(p.E581K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000446176 |
| Start | 129902963:129902963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1334A>G |
| AA Mutation | p.Asn445Ser(p.N445S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000446176 |
| Start | 129925070:129925070(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758733709 |
| CDS Mutation | c.877C>T |
| AA Mutation | p.Arg293Cys(p.R293C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000446176 |
| Start | 129900029:129900029(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs541613536 |
| CDS Mutation | c.1623C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |