A8T (p.Ala8Thr) variant of NPR1 (P16066)
A8T (p.Ala8Thr) in NPR1 (P16066) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data and structural context.
A8T (p.Ala8Thr) variant details
- p.Ala8Thr
- ExAC rs767857443
- gnomAD rs767857443
- Missense
- Variant Prioritization Score for Impact Estimate 0.165
- REVEL 0.20
- CADD 7.13
- PolyPhen-2 0.00
- SIFT 0.56
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available