Annotation Detail
Information
- Associated Genes
- ACTG1
- Associated Variants
-
ACTG1 p.Arg256Trp (p.R256W)
(
ENST00000571721.6,
ENST00000575994.6,
ENST00000575842.5,
ENST00000571691.6,
ENST00000615544.5,
ENST00000575659.6,
ENST00000570382.2,
ENST00000679480.1,
ENST00000575087.5,
ENST00000681052.1,
ENST00000644774.2,
ENST00000573283.7 )
ACTG1 p.Arg256Trp (p.R256W) ( ENST00000570382.2, ENST00000571691.6, ENST00000571721.6, ENST00000573283.7, ENST00000575087.5, ENST00000575659.6, ENST00000575842.5, ENST00000575994.6, ENST00000615544.5, ENST00000644774.2, ENST00000679480.1, ENST00000681052.1 ) - Associated Disease
- Autosomal dominant nonsyndromic hearing loss 20
- Source Database
- ClinVar
- Description
- NM_001614.5(ACTG1):c.766C>T (p.Arg256Trp) AND Autosomal dominant nonsyndromic hearing loss 20
- ClinVar Allele ID
- 38544
- ClinVar RefSeq Alternation Syntax
- NM_001199954.3:c.766C>T
- ClinVar RefSeq Alternation Syntax
- NR_037688.3:n.838C>T
- ClinVar RefSeq Alternation Syntax
- NM_001614.5:c.766C>T
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2019-02-26
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000770804
- ClinVar Disease
- Autosomal dominant nonsyndromic hearing loss 20
- Observed Origin Sample
- inherited
Drugs