S41G (p.Ser41Gly) variant of PADI4 (Q9UM07)
S41G (p.Ser41Gly) in PADI4 (Q9UM07) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data, published literature, and structural context.
S41G (p.Ser41Gly) variant details
- p.Ser41Gly
- gnomAD 1-17330997-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.0801
- REVEL 0.04
- CADD 10.20
- PolyPhen-2 0.02
- SIFT 0.44
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available
- Literature evidence available