S97F (p.Ser97Phe) variant of HNRNPU (Q00839)
S97F (p.Ser97Phe) in HNRNPU (Q00839) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as likely benign in the context of Developmental and epileptic encephalopathy, 54. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data, published literature, and structural context.
S97F (p.Ser97Phe) variant details
- p.Ser97Phe
- rs1479183749
- ClinGen CA345497450
- ClinVar RCV002553496
- gnomAD rs1479183749
- Likely benign
- Developmental and epileptic encephalopathy, 54
- Missense
- Variant Prioritization Score for Impact Estimate 0.284
- REVEL 0.11
- ESM-1b 0.00
- AlphaMissense 0.13
- CADD 23.30
- PolyPhen-2 0.00
- SIFT 0.05
- ClinVar: Likely benign (Developmental and epileptic encephalopathy, 54)
- EBI: Likely benign
- UniProt: Likely benign
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Cited in: HNRNPU-Related Neurodevelopmental Disorder. (PMID 35274911)