Primary Site >> Stomach Cancer
Gene >> HDAC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373548 |
| Start | 32331708:32331708(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1121C>T |
| AA Mutation | p.Pro374Leu(p.P374L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373548 |
| Start | 32327650:32327650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.609G>T |
| AA Mutation | p.Glu203Asp(p.E203D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373548 |
| Start | 32327019:32327019(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.436G>A |
| AA Mutation | p.Glu146Lys(p.E146K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373548 |
| Start | 32330851:32330851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747301084 |
| CDS Mutation | c.922G>A |
| AA Mutation | p.Val308Ile(p.V308I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373548 |
| Start | 32327659:32327659(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.618A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373548 |
| Start | 32331778:32331778(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs552958105 |
| CDS Mutation | c.1191C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |