S2N (p.Ser2Asn) variant of BAG3 (O95817)
S2N (p.Ser2Asn) 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 0.49 / 1. The record also includes population frequency data, experimental measurements, published literature, and structural context.
S2N (p.Ser2Asn) variant details
- p.Ser2Asn
- rs1396002893
- ClinGen CA378293972
- ClinVar RCV001889635
- ClinVar RCV003382689
- Uncertain significance
- Dilated cardiomyopathy 1HH; Myofibrillar myopathy 6; Cardiovascular phenotype
- Missense
- Variant Prioritization Score for Impact Estimate 0.486
- REVEL 0.33
- CADD 23.40
- PolyPhen-2 0.34
- 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 1.6e-05)
- Structural context available
- BAG3 WW domain domainome 1.0: score 0.199
- 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)