Q157R (p.Gln157Arg) variant of CHM (P24386)
Q157R (p.Gln157Arg) in CHM (P24386) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data and structural context.
Q157R (p.Gln157Arg) variant details
- p.Gln157Arg
- TOPMed rs1930431444
- gnomAD rs1930431444
- Missense
- Variant Prioritization Score for Impact Estimate 0.105
- REVEL 0.03
- MetaLR 0.10
- MetaSVM -1.02
- CADD 11.80
- PolyPhen-2 0.00
- SIFT 0.34
- Most common in the Non-Finnish European population (allele frequency 1.9e-05)
- Structural context available