L27del (p.Leu27del) variant of NPR1 (P16066)
L27del (p.Leu27del) 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.
L27del (p.Leu27del) variant details
- rs774440887
- gnomAD 1-153679173-CGCT-
- Inframe Deletion
- Variant Prioritization Score for Impact Estimate 0.161
- CADD 11.40
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available
- Literature evidence available