D29G (p.Asp29Gly) variant of RECQL4 (ATP-dependent DNA helicase Q4)
D29G (p.Asp29Gly) in RECQL4 (ATP-dependent DNA helicase Q4) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Baller-Gerold syndrome. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data, published literature, and structural context.
D29G (p.Asp29Gly) variant details
- p.Asp29Gly
- rs2538130001
- ClinGen CA372693557
- ClinVar RCV002676611
- Uncertain significance
- Baller-Gerold syndrome
- Missense
- Variant Prioritization Score for Impact Estimate 0.176
- CADD 16.00
- PolyPhen-2 0.01
- SIFT 0.13
- ClinVar: Uncertain significance (Baller-Gerold syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Population evidence available
- Structural context available
- Cited in: Baller-Gerold Syndrome. (PMID 20301383)