F39S (p.Phe39Ser) variant of BAG3 (O95817)
F39S (p.Phe39Ser) in BAG3 (O95817) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Dilated cardiomyopathy 1HH; Myofibrillar myopathy 6; Cardiovascular phenotype. The available variant effect predictions contribute to a CATVariant prioritization score of 0.80 / 1. The record also includes population frequency data, experimental measurements, published literature, and structural context.
F39S (p.Phe39Ser) variant details
- p.Phe39Ser
- rs1472915271
- ClinGen CA378294211
- ClinVar RCV001904080
- ClinVar RCV002331360
- Uncertain significance
- Dilated cardiomyopathy 1HH; Myofibrillar myopathy 6; Cardiovascular phenotype
- Missense
- Variant Prioritization Score for Impact Estimate 0.801
- REVEL 0.90
- CADD 32.00
- PolyPhen-2 1.00
- SIFT 0.00
- ClinVar: Uncertain significance (Dilated cardiomyopathy 1HH; Myofibrillar myopathy 6; Cardiovascu)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 2.3e-05)
- Structural context available
- BAG3 WW domain domainome 1.0: score -0.205
- Cited in: Dilated Cardiomyopathy Overview. (PMID 20301486)
- Cited in: ACMG SF v3.1 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of… (PMID 35802134)