p.Pro21 Leu26del variant of NPR1 (P16066)
p.Pro21 Leu26del in NPR1 (P16066) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data, published literature, and structural context.
p.Pro21 Leu26del variant details
- gnomAD 1-153679159-CCTGC
- Inframe Deletion
- Variant Prioritization Score for Impact Estimate 0.176
- CADD 13.40
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available
- Literature evidence available