G19V (p.Gly19Val) variant of DAP3 (P51398)
G19V (p.Gly19Val) in DAP3 (P51398) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data, published literature, and structural context.
G19V (p.Gly19Val) variant details
- p.Gly19Val
- gnomAD 1-155717016-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.284
- REVEL 0.15
- ESM-1b 0.00
- AlphaMissense 0.10
- CADD 18.80
- PolyPhen-2 0.01
- SIFT 0.08
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available