P58T (p.Pro58Thr) variant of BLM (RecQ-like DNA helicase BLM)
P58T (p.Pro58Thr) 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 0.34 / 1. The record also includes published literature and structural context.
P58T (p.Pro58Thr) variant details
- p.Pro58Thr
- rs1596217837
- ClinGen CA393839557
- ClinVar RCV000792917
- ClinVar RCV001012877
- Uncertain significance
- Hereditary cancer-predisposing syndrome; Bloom syndrome
- Missense
- Variant Prioritization Score for Impact Estimate 0.344
- AlphaMissense 0.07
- MetaLR 0.15
- MetaSVM -0.93
- PolyPhen-2 0.97
- SIFT 0.05
- MutPred 0.43
- 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)