Annotation Detail
Information
- Associated Genes
- ACTG1
- Associated Variants
-
ACTG1 p.Ser155Phe (p.S155F)
(
ENST00000679480.1,
ENST00000575087.5,
ENST00000575659.6,
ENST00000615544.5,
ENST00000570382.2,
ENST00000681052.1,
ENST00000573283.7,
ENST00000644774.2,
ENST00000571721.6,
ENST00000575994.6,
ENST00000575842.5,
ENST00000571691.6 )
ACTG1 p.Ser155Phe (p.S155F) ( 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
- Inborn genetic diseases
- Source Database
- ClinVar
- Description
- NM_001614.5(ACTG1):c.464C>T (p.Ser155Phe) AND Inborn genetic diseases
- ClinVar Allele ID
- 38539
- ClinVar RefSeq Alternation Syntax
- NM_001199954.3:c.464C>T
- ClinVar RefSeq Alternation Syntax
- NM_001614.5:c.464C>T
- ClinVar RefSeq Alternation Syntax
- NR_037688.3:n.536C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2023-08-17
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003362663
- ClinVar Disease
- Inborn genetic diseases
- Observed Origin Sample
- germline
Drugs