L9V (p.Leu9Val) variant of DAP3 (P51398)
L9V (p.Leu9Val) 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.
L9V (p.Leu9Val) variant details
- p.Leu9Val
- TOPMed rs1656470831
- gnomAD rs1656470831
- Missense
- Variant Prioritization Score for Impact Estimate 0.13
- REVEL 0.02
- ESM-1b 0.00
- AlphaMissense 0.08
- CADD 17.00
- PolyPhen-2 0.01
- SIFT 0.06
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available