P137S (p.Pro137Ser) variant of SMARCE1 (Q969G3)
P137S (p.Pro137Ser) in SMARCE1 (Q969G3) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome; Familial meningioma. The available variant effect predictions contribute to a CATVariant prioritization score of 0.75 / 1. The record also includes published literature and structural context.
P137S (p.Pro137Ser) variant details
- p.Pro137Ser
- rs2143996465
- ClinGen CA399366654
- ClinVar RCV001900631
- ClinVar RCV002324268
- Uncertain significance
- Hereditary cancer-predisposing syndrome; Familial meningioma
- Missense
- Variant Prioritization Score for Impact Estimate 0.751
- AlphaMissense 0.94
- MetaLR 0.91
- MetaSVM 1.00
- PolyPhen-2 0.26
- SIFT 0.02
- EVE 0.46
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome; Familial meningioma)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- 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)