Primary Site >> Stomach Cancer
Gene >> HMGCR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287936 |
| Start | 75359263:75359263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2251G>A |
| AA Mutation | p.Ala751Thr(p.A751T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287936 |
| Start | 75347250:75347250(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.497C>T |
| AA Mutation | p.Pro166Leu(p.P166L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287936 |
| Start | 75350145:75350145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.660A>C |
| AA Mutation | p.Leu220Phe(p.L220F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287936 |
| Start | 75351465:75351465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781331129 |
| CDS Mutation | c.1231A>C |
| AA Mutation | p.Asn411His(p.N411H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287936 |
| Start | 75354618:75354618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1484G>A |
| AA Mutation | p.Arg495His(p.R495H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287936 |
| Start | 75355435:75355435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1793G>A |
| AA Mutation | p.Arg598His(p.R598H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000287936 |
| Start | 75359262:75359262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201738996 |
| CDS Mutation | c.2250C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |