Primary Site >> Stomach Cancer
Gene >> GRB7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309156 |
| Start | 39744620:39744620(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138362707 |
| CDS Mutation | c.869G>A |
| AA Mutation | p.Arg290His(p.R290H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000309156 |
| Start | 39745788:39745788(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1270G>A |
| AA Mutation | p.Ala424Thr(p.A424T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309156 |
| Start | 39744598:39744598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751537147 |
| CDS Mutation | c.847G>A |
| AA Mutation | p.Val283Met(p.V283M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309156 |
| Start | 39742919:39742919(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.328G>A |
| AA Mutation | p.Asp110Asn(p.D110N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309156 |
| Start | 39744920:39744920(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371514592 |
| CDS Mutation | c.947G>A |
| AA Mutation | p.Arg316Gln(p.R316Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309156 |
| Start | 39745444:39745444(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1115T>C |
| AA Mutation | p.Leu372Pro(p.L372P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309156 |
| Start | 39745759:39745759(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1241T>C |
| AA Mutation | p.Met414Thr(p.M414T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000309156 |
| Start | 39742358:39742358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778062709 |
| CDS Mutation | c.57A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |