A39G (p.Ala39Gly) variant of GNAS (P63092)
A39G (p.Ala39Gly) in GNAS (P63092) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.77 / 1. The record also includes population frequency data, published literature, and structural context.
A39G (p.Ala39Gly) variant details
- p.Ala39Gly
- rs1449469660
- gnomAD 20-58840198-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.766
- CADD 26.80
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available