H14D (p.His14Asp) variant of DAP3 (P51398)
H14D (p.His14Asp) 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 and structural context.
H14D (p.His14Asp) variant details
- p.His14Asp
- gnomAD rs1397911722
- Missense
- Variant Prioritization Score for Impact Estimate 0.131
- REVEL 0.02
- ESM-1b 0.00
- AlphaMissense 0.08
- CADD 15.90
- PolyPhen-2 0.01
- SIFT 0.20
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available