Annotation Detail
Information
- Associated Genes
- HBB LOC106099062 LOC107133510
- Associated Variants
-
HBB p.Val99Met (p.V99M)
(
ENST00000647020.1,
ENST00000335295.4,
ENST00000485743.1 )
HBB p.Leu33Gln (p.L33Q) ( ENST00000647020.1, ENST00000485743.1, ENST00000335295.4 )
HBB p.Val99Met (p.V99M) ( ENST00000335295.4, ENST00000485743.1, ENST00000647020.1 )
HBB p.Leu33Gln (p.L33Q) ( ENST00000335295.4, ENST00000485743.1, ENST00000647020.1 ) - Source Database
- ClinVar
- Description
- NM_000518.4(HBB):c.[295G>A;98T>A] AND HEMOGLOBIN MEDICINE LAKE
- ClinVar Allele ID
- 30572
- ClinVar Allele ID
- 30280
- ClinVar RefSeq Alternation Syntax
- NM_000518.5:c.98T>A
- ClinVar RefSeq Alternation Syntax
- NM_000518.5:c.295G>A
- Clinical Significance Description
- other
- Clinical Significance Last Update
- 2017-12-12
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000016807
- Observed Origin Sample
- germline
- Pubmed
- 7860732
Drugs