p.Leu20dup variant of NPR1 (P16066)
p.Leu20dup in NPR1 (P16066) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data, published literature, and structural context.
p.Leu20dup variant details
- gnomAD 1-153679159-C-CCT
- Inframe Insertion
- Variant Prioritization Score for Impact Estimate 0.155
- CADD 10.50
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)
- Structural context available
- Literature evidence available