D17V (p.Asp17Val) variant of DAP3 (P51398)
D17V (p.Asp17Val) in DAP3 (P51398) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data and structural context.
D17V (p.Asp17Val) variant details
- p.Asp17Val
- gnomAD rs1345656156
- Missense
- Variant Prioritization Score for Impact Estimate 0.203
- REVEL 0.06
- ESM-1b 0.00
- AlphaMissense 0.11
- CADD 21.90
- PolyPhen-2 0.01
- SIFT 0.03
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available