R29H (p.Arg29His) variant of DAP3 (P51398)
R29H (p.Arg29His) in DAP3 (P51398) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data and structural context.
R29H (p.Arg29His) variant details
- p.Arg29His
- ESP rs369774038
- ExAC rs369774038
- TOPMed rs369774038
- gnomAD rs369774038
- Missense
- Variant Prioritization Score for Impact Estimate 0.146
- REVEL 0.04
- ESM-1b 0.00
- AlphaMissense 0.07
- CADD 4.73
- PolyPhen-2 0.00
- SIFT 0.25
- Most common in the Latino/Admixed American population (allele frequency 6.6e-05)
- Structural context available