H16D (p.His16Asp) variant of PADI4 (Q9UM07)
H16D (p.His16Asp) in PADI4 (Q9UM07) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data and structural context.
H16D (p.His16Asp) variant details
- p.His16Asp
- gnomAD rs1233872154
- Missense
- Variant Prioritization Score for Impact Estimate 0.338
- REVEL 0.09
- CADD 14.80
- PolyPhen-2 0.19
- SIFT 0.03
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available