T38M (p.Thr38Met) variant of PADI4 (Q9UM07)
T38M (p.Thr38Met) in PADI4 (Q9UM07) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes population frequency data and structural context.
T38M (p.Thr38Met) variant details
- p.Thr38Met
- ExAC rs748929537
- TOPMed rs748929537
- gnomAD rs748929537
- Missense
- Variant Prioritization Score for Impact Estimate 0.221
- REVEL 0.07
- CADD 24.10
- PolyPhen-2 0.97
- SIFT 0.04
- Most common in the African/African-American population (allele frequency 4.8e-05)
- Structural context available