Primary Site >> Stomach Cancer
Gene >> BCAP29
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000005259 |
| Start | 107613342:107613342(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.600G>T |
| AA Mutation | p.Lys200Asn(p.K200N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000005259 |
| Start | 107600470:107600470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.554A>G |
| AA Mutation | p.Glu185Gly(p.E185G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000005259 |
| Start | 107594017:107594017(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.256A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000005259 |
| Start | 107594016:107594016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.255C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000005259 |
| Start | 107618336:107618336(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.699A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000005259 |
| Start | 107594095:107594095(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs779181657 |
| CDS Mutation | c.340delT |
| AA Mutation | p.Trp114GlyfsTer2(p.W114Gfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |