P66S (p.Pro66Ser) variant of PPP2R5D (Q14738)
P66S (p.Pro66Ser) in PPP2R5D (Q14738) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data, published literature, and structural context.
P66S (p.Pro66Ser) variant details
- p.Pro66Ser
- gnomAD 6-43006553-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.388
- REVEL 0.17
- CADD 17.40
- PolyPhen-2 0.00
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available