Annotation Detail
Information
- Associated Genes
- HBB LOC106099062 LOC107133510
- Associated Variants
-
HBB p.Phe86Ser (p.F86S)
(
ENST00000647020.1,
ENST00000335295.4,
ENST00000485743.1 )
HBB p.Phe86Ser (p.F86S) ( ENST00000335295.4, ENST00000485743.1, ENST00000647020.1 ) - Associated Disease
- hemoglobinopathy
- Source Database
- ClinVar
- Description
- NM_000518.5(HBB):c.257T>C (p.Phe86Ser) AND Hemoglobinopathy
- ClinVar Allele ID
- 30161
- ClinVar RefSeq Alternation Syntax
- NM_000518.5:c.257T>C
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 1967-09-29
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000016279
- ClinVar Disease
- Hemoglobinopathy
- Observed Origin Sample
- germline
- Pubmed
- 6038175
- Pubmed
- 14197371
Drugs