S237F (p.Ser237Phe) variant of PURA (Q00577)
S237F (p.Ser237Phe) in PURA (Q00577) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as likely pathogenic in the context of PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome. The available variant effect predictions contribute to a CATVariant prioritization score of 0.50 / 1. The record also includes published literature and structural context.
S237F (p.Ser237Phe) variant details
- p.Ser237Phe
- rs886039899
- ClinGen CA10588951
- ClinVar RCV000256438
- Ensembl rs886039899
- Likely pathogenic
- PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome
- Missense
- Variant Prioritization Score for Impact Estimate 0.503
- ESM-1b 1.00
- AlphaMissense 0.65
- MetaLR 0.19
- MetaSVM -0.78
- PolyPhen-2 1.00
- SIFT 0.05
- ClinVar: Likely pathogenic (PURA-related severe neonatal hypotonia-seizures-encephalopathy s)
- EBI: Likely pathogenic
- UniProt: Likely pathogenic
- Structural context available
- Cited in: PURA-Related Neurodevelopmental Disorders. (PMID 28448108)