S30T (p.Ser30Thr) variant of NPR1 (P16066)
S30T (p.Ser30Thr) in NPR1 (P16066) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data, published literature, and structural context.
S30T (p.Ser30Thr) variant details
- p.Ser30Thr
- gnomAD 1-153679197-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.197
- REVEL 0.16
- CADD 6.31
- PolyPhen-2 0.00
- SIFT 0.60
- Most common in the 1KG:MSL population (allele frequency 0.013)
- Structural context available
- Literature evidence available