P2T (p.Pro2Thr) variant of NPR1 (P16066)
P2T (p.Pro2Thr) in NPR1 (P16066) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data and structural context.
P2T (p.Pro2Thr) variant details
- p.Pro2Thr
- gnomAD rs1669681743
- Missense
- Variant Prioritization Score for Impact Estimate 0.252
- REVEL 0.23
- CADD 16.00
- PolyPhen-2 0.02
- SIFT 0.00
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available