N69H (p.Asn69His) variant of DAP3 (P51398)
N69H (p.Asn69His) in DAP3 (P51398) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data, published literature, and structural context.
N69H (p.Asn69His) variant details
- p.Asn69His
- gnomAD 1-155721553-A-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.156
- REVEL 0.07
- ESM-1b 0.00
- AlphaMissense 0.06
- CADD 20.90
- PolyPhen-2 0.00
- SIFT 0.04
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)
- Structural context available
- Literature evidence available