Primary Site >> Stomach Cancer
Gene >> RUNX1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344691 |
| Start | 34792541:34792541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.956G>A |
| AA Mutation | p.Arg319His(p.R319H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344691 |
| Start | 34834502:34834502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.632T>C |
| AA Mutation | p.Val211Ala(p.V211A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344691 |
| Start | 34799344:34799344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.843C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344691 |
| Start | 34799440:34799440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.747C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344691 |
| Start | 34799368:34799368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs533383085 |
| CDS Mutation | c.819G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344691 |
| Start | 34880621:34880621(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773689002 |
| CDS Mutation | c.363C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |