N38D (p.Asn38Asp) variant of DAP3 (P51398)
N38D (p.Asn38Asp) in DAP3 (P51398) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, published literature, and structural context.
N38D (p.Asn38Asp) variant details
- p.Asn38Asp
- gnomAD 1-155717072-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.0876
- REVEL 0.03
- ESM-1b 0.00
- AlphaMissense 0.06
- CADD 7.68
- Most common in the East Asian population (allele frequency 0.00019)
- Structural context available
- Literature evidence available