V52M (p.Val52Met) variant of BLM (RecQ-like DNA helicase BLM)
V52M (p.Val52Met) in BLM (RecQ-like DNA helicase BLM) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome; Bloom syndrome; not provided. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data, published literature, and structural context.
V52M (p.Val52Met) variant details
- p.Val52Met
- rs2151146745
- ClinGen CA393839494
- ClinVar RCV002023018
- ClinVar RCV003478923
- Uncertain significance
- Hereditary cancer-predisposing syndrome; Bloom syndrome; not provided
- Missense
- Variant Prioritization Score for Impact Estimate 0.174
- REVEL 0.03
- CADD 11.40
- PolyPhen-2 0.03
- SIFT 0.09
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome; Bloom syndrome; not pro)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Cited in: Carrier screening in individuals of Ashkenazi Jewish descent. (PMID 18197057)
- Cited in: ACOG Committee Opinion No. 442: Preconception and prenatal carrier screening for genetic diseases in individuals of… (PMID 19888064)