Primary Site >> Stomach Cancer
Gene >> CYC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318911 |
| Start | 144097251:144097251(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.893T>C |
| AA Mutation | p.Leu298Pro(p.L298P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318911 |
| Start | 144096736:144096736(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.764T>G |
| AA Mutation | p.Phe255Cys(p.F255C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318911 |
| Start | 144097289:144097289(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.931T>C |
| AA Mutation | p.Trp311Arg(p.W311R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318911 |
| Start | 144095870:144095870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.167G>A |
| AA Mutation | p.Gly56Asp(p.G56D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000318911 |
| Start | 144096202:144096202(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.405G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000318911 |
| Start | 144095949:144095949(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs538272583 |
| CDS Mutation | c.246G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |