N37S (p.Asn37Ser) variant of SMARCE1 (Q969G3)
N37S (p.Asn37Ser) in SMARCE1 (Q969G3) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as conflicting interpretations in the context of Hereditary cancer-predisposing syndrome; Familial meningioma. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data, experimental measurements, published literature, and structural context.
N37S (p.Asn37Ser) variant details
- p.Asn37Ser
- rs1597749763
- ClinGen CA399369770
- ClinVar RCV001017350
- ClinVar RCV001208204
- Conflicting interpretations
- Hereditary cancer-predisposing syndrome; Familial meningioma
- Missense
- Variant Prioritization Score for Impact Estimate 0.324
- REVEL 0.10
- CADD 23.90
- PolyPhen-2 0.94
- SIFT 0.17
- ClinVar: Conflicting classifications of pathogenicity (Hereditary cancer-predisposing syndrome; Familial meningioma)
- EBI: Likely benign
- UniProt: Likely benign
- Most common in the Middle Eastern population (allele frequency 0.0002)
- Structural context available
- SMARCE1 High mobility group box domain domainome 1.0: score -0.976
- Cited in: MN1 C-Terminal Truncation Syndrome. (PMID 32790267)
- Cited in: A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic… (PMID 25394175)