H35D (p.His35Asp) variant of DAP3 (P51398)
H35D (p.His35Asp) in DAP3 (P51398) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data, published literature, and structural context.
H35D (p.His35Asp) variant details
- p.His35Asp
- gnomAD 1-155717063-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.13
- REVEL 0.02
- ESM-1b 0.00
- AlphaMissense 0.07
- CADD 10.30
- PolyPhen-2 0.01
- SIFT 0.60
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available