L8M (p.Leu8Met) variant of SMARCA4 (P51532)
L8M (p.Leu8Met) in SMARCA4 (P51532) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome; Rhabdoid tumor predisposition syndrome. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes published literature and structural context.
L8M (p.Leu8Met) variant details
- p.Leu8Met
- rs1555750596
- ClinGen CA404053890
- ClinVar RCV002446300
- ClinVar RCV003101209
- Uncertain significance
- Hereditary cancer-predisposing syndrome; Rhabdoid tumor predisposition syndrome
- Missense
- Variant Prioritization Score for Impact Estimate 0.381
- AlphaMissense 0.08
- MetaLR 0.30
- MetaSVM -0.76
- PolyPhen-2 0.01
- SIFT 0.04
- MutPred 0.20
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome; Rhabdoid tumor predispo)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- Cited in: A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic… (PMID 25394175)
- Cited in: Rhabdoid Tumor Predisposition Syndrome. (PMID 29215836)