L27F (p.Leu27Phe) variant of BLM (RecQ-like DNA helicase BLM)
L27F (p.Leu27Phe) 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. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes published literature and structural context.
L27F (p.Leu27Phe) variant details
- p.Leu27Phe
- rs1368566341
- ClinGen CA393838977
- ClinVar RCV002419144
- ClinVar RCV003776468
- Uncertain significance
- Hereditary cancer-predisposing syndrome; Bloom syndrome
- Missense
- Variant Prioritization Score for Impact Estimate 0.313
- AlphaMissense 0.07
- MetaLR 0.08
- MetaSVM -1.03
- PolyPhen-2 0.00
- SIFT 0.10
- MutPred 0.18
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome; Bloom syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- 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)