A37G (p.Ala37Gly) variant of GRN (Progranulin)
A37G (p.Ala37Gly) in GRN (Progranulin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data, published literature, and structural context.
A37G (p.Ala37Gly) variant details
- p.Ala37Gly
- gnomAD 17-44349274-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.184
- REVEL 0.12
- CADD 13.10
- PolyPhen-2 0.43
- SIFT 0.34
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)
- Structural context available
- Literature evidence available