V18A (p.Val18Ala) variant of PADI4 (Q9UM07)
V18A (p.Val18Ala) in PADI4 (Q9UM07) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.43 / 1. The record also includes population frequency data and structural context.
V18A (p.Val18Ala) variant details
- p.Val18Ala
- TOPMed rs894020390
- gnomAD rs894020390
- Missense
- Variant Prioritization Score for Impact Estimate 0.43
- REVEL 0.28
- CADD 25.40
- PolyPhen-2 1.00
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available