G39A (p.Gly39Ala) variant of MAPK3 (P27361)
G39A (p.Gly39Ala) in MAPK3 (P27361) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data and structural context.
G39A (p.Gly39Ala) variant details
- p.Gly39Ala
- gnomAD rs2073034354
- Missense
- Variant Prioritization Score for Impact Estimate 0.298
- REVEL 0.08
- CADD 22.50
- PolyPhen-2 0.00
- SIFT 0.11
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available