C151R (p.Cys151Arg) variant of CHM (P24386)
C151R (p.Cys151Arg) in CHM (P24386) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data and structural context.
C151R (p.Cys151Arg) variant details
- p.Cys151Arg
- TOPMed rs1930433761
- Missense
- Variant Prioritization Score for Impact Estimate 0.173
- REVEL 0.06
- MetaLR 0.44
- MetaSVM -0.70
- CADD 11.60
- PolyPhen-2 0.00
- SIFT 0.54
- Most common in the Non-Finnish European population (allele frequency 3.6e-06)
- Structural context available