Primary Site >> Stomach Cancer
Gene >> BCAR1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000162330 |
| Start | 75229819:75229819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757527015 |
| CDS Mutation | c.2305G>A |
| AA Mutation | p.Val769Met(p.V769M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000162330 |
| Start | 75235805:75235805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769456547 |
| CDS Mutation | c.1094C>T |
| AA Mutation | p.Pro365Leu(p.P365L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000162330 |
| Start | 75235722:75235722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140889740 |
| CDS Mutation | c.1177C>T |
| AA Mutation | p.Arg393Trp(p.R393W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000162330 |
| Start | 75229834:75229834(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769103790 |
| CDS Mutation | c.2290G>A |
| AA Mutation | p.Ala764Thr(p.A764T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000162330 |
| Start | 75235137:75235137(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs561070895 |
| CDS Mutation | c.1762G>A |
| AA Mutation | p.Glu588Lys(p.E588K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000162330 |
| Start | 75234902:75234902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1997A>G |
| AA Mutation | p.Tyr666Cys(p.Y666C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000162330 |
| Start | 75243074:75243074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.29C>T |
| AA Mutation | p.Ala10Val(p.A10V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000162330 |
| Start | 75229699:75229699(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761352041 |
| CDS Mutation | c.2425C>T |
| AA Mutation | p.Arg809Cys(p.R809C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000162330 |
| Start | 75229867:75229867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750624866 |
| CDS Mutation | c.2257G>A |
| AA Mutation | p.Ala753Thr(p.A753T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000162330 |
| Start | 75242829:75242829(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.274C>A |
| AA Mutation | p.Pro92Thr(p.P92T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000162330 |
| Start | 75242962:75242962(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.141G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000162330 |
| Start | 75242539:75242539(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756162089 |
| CDS Mutation | c.564G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000162330 |
| Start | 75242824:75242824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748135777 |
| CDS Mutation | c.279G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000162330 |
| Start | 75237210:75237210(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.768delG |
| AA Mutation | p.Leu257CysfsTer56(p.L257Cfs*56) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |