A32T (p.Ala32Thr) variant of NPR1 (P16066)
A32T (p.Ala32Thr) in NPR1 (P16066) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data and structural context.
A32T (p.Ala32Thr) variant details
- p.Ala32Thr
- TOPMed rs1243141793
- gnomAD rs1243141793
- Missense
- Variant Prioritization Score for Impact Estimate 0.331
- REVEL 0.18
- CADD 15.10
- PolyPhen-2 0.15
- SIFT 0.31
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Structural context available