H33Q (p.His33Gln) variant of NLRP1 (Q9C000)
H33Q (p.His33Gln) in NLRP1 (Q9C000) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data.
H33Q (p.His33Gln) variant details
- p.His33Gln
- ExAC rs757234714
- gnomAD rs757234714
- Missense
- Variant Prioritization Score for Impact Estimate 0.0859
- CADD 3.40
- PolyPhen-2 0.15
- SIFT 0.29
- Most common in the Latino/Admixed American population (allele frequency 2.5e-05)