Primary Site >> Stomach Cancer
Gene >> BTRC
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370187 |
| Start | 101430435:101430435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752077302 |
| CDS Mutation | c.139G>A |
| AA Mutation | p.Ala47Thr(p.A47T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370187 |
| Start | 101536604:101536604(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1528C>T |
| AA Mutation | p.Arg510Cys(p.R510C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370187 |
| Start | 101535367:101535367(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1361G>A |
| AA Mutation | p.Ser454Asn(p.S454N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370187 |
| Start | 101535406:101535406(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1400G>A |
| AA Mutation | p.Arg467Gln(p.R467Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370187 |
| Start | 101534731:101534731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1168C>T |
| AA Mutation | p.Arg390Cys(p.R390C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000370187 |
| Start | 101536653:101536653(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1577G>A |
| AA Mutation | p.Gly526Glu(p.G526E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370187 |
| Start | 101534697:101534697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373104717 |
| CDS Mutation | c.1134G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370187 |
| Start | 101462013:101462013(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759103744 |
| CDS Mutation | c.189C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000370187 |
| Start | 101550816:101550816(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1780delC |
| AA Mutation | p.Arg594ValfsTer14(p.R594Vfs*14) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000370187 |
| Start | 101532312:101532312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.858G>A |
| AA Mutation | p.Trp286Ter(p.W286*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000370187 |
| Start | 101550815:101550816(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs774921343 |
| CDS Mutation | c.1780dupC |
| AA Mutation | p.Arg594ProfsTer27(p.R594Pfs*27) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |