Primary Site >> Stomach Cancer
Gene >> HID1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000425042 |
| Start | 74951608:74951608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2329G>A |
| AA Mutation | p.Asp777Asn(p.D777N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000425042 |
| Start | 74960174:74960174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.803A>G |
| AA Mutation | p.Tyr268Cys(p.Y268C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000425042 |
| Start | 74958383:74958383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1336C>T |
| AA Mutation | p.Arg446Cys(p.R446C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000425042 |
| Start | 74960085:74960085(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.892A>G |
| AA Mutation | p.Ser298Gly(p.S298G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000425042 |
| Start | 74963804:74963804(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.323T>C |
| AA Mutation | p.Ile108Thr(p.I108T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000425042 |
| Start | 74951630:74951630(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2307T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000425042 |
| Start | 74960185:74960185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144217591 |
| CDS Mutation | c.792C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |