p.Leu27dup variant of NPR1 (P16066)
p.Leu27dup 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.Leu27dup variant details
- rs774440887
- gnomAD 1-153679173-C-CGC
- Inframe Insertion
- Variant Prioritization Score for Impact Estimate 0.16
- CADD 11.20
- Most common in the African/African-American population (allele frequency 0.00041)
- Structural context available
- Literature evidence available