P66S (p.Pro66Ser) variant of NPPB (Natriuretic peptides B)
P66S (p.Pro66Ser) in NPPB (Natriuretic peptides B) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, published literature, and structural context.
P66S (p.Pro66Ser) variant details
- p.Pro66Ser
- gnomAD 1-11858406-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.088
- REVEL 0.08
- CADD 5.00
- PolyPhen-2 0.25
- SIFT 0.12
- Most common in the Non-Finnish European population (allele frequency 9.2e-07)
- Structural context available
- Literature evidence available