P39S (p.Pro39Ser) variant of RINL (Q6ZS11)
P39S (p.Pro39Ser) in RINL (Q6ZS11) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data and structural context.
P39S (p.Pro39Ser) variant details
- p.Pro39Ser
- TOPMed rs769778468
- gnomAD rs769778468
- Missense
- Variant Prioritization Score for Impact Estimate 0.323
- CADD 14.60
- PolyPhen-2 0.00
- SIFT 0.12
- Population evidence available
- Structural context available