S37G (p.Ser37Gly) variant of FOXP2 (Forkhead box protein P2)
S37G (p.Ser37Gly) in FOXP2 (Forkhead box protein P2) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data, published literature, and structural context.
S37G (p.Ser37Gly) variant details
- p.Ser37Gly
- gnomAD 7-114426620-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.327
- REVEL 0.08
- MetaLR 0.61
- MetaSVM 0.12
- CADD 22.60
- PolyPhen-2 0.06
- SIFT 0.29
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available