Q37R (p.Gln37Arg) variant of PPP2R5D (Q14738)
Q37R (p.Gln37Arg) in PPP2R5D (Q14738) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data, published literature, and structural context.
Q37R (p.Gln37Arg) variant details
- p.Gln37Arg
- gnomAD 6-43006467-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.283
- REVEL 0.16
- CADD 17.00
- PolyPhen-2 0.01
- SIFT 0.11
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available