R13L (p.Arg13Leu) variant of NPR1 (P16066)
R13L (p.Arg13Leu) in NPR1 (P16066) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data and structural context.
R13L (p.Arg13Leu) variant details
- p.Arg13Leu
- ExAC rs13305997
- TOPMed rs13305997
- gnomAD rs13305997
- Missense
- Variant Prioritization Score for Impact Estimate 0.236
- REVEL 0.29
- CADD 14.00
- PolyPhen-2 0.02
- SIFT 0.28
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available