R79H (p.Arg79His) variant of COMP (P49747)
R79H (p.Arg79His) in COMP (P49747) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.05 / 1. The record also includes population frequency data and structural context.
R79H (p.Arg79His) variant details
- p.Arg79His
- 1000Genomes rs578030956
- ExAC rs578030956
- TOPMed rs578030956
- gnomAD rs578030956
- Missense
- Variant Prioritization Score for Impact Estimate 0.0542
- REVEL 0.01
- ESM-1b 0.00
- AlphaMissense 0.07
- CADD 3.07
- PolyPhen-2 0.00
- SIFT 0.07
- Population evidence available
- Structural context available