R77G (p.Arg77Gly) variant of MAPK1 (P28482)
R77G (p.Arg77Gly) in MAPK1 (P28482) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.56 / 1. The record also includes population frequency data, experimental measurements, and structural context.
R77G (p.Arg77Gly) variant details
- p.Arg77Gly
- gnomAD rs1330050442
- Missense
- Variant Prioritization Score for Impact Estimate 0.565
- REVEL 0.56
- CADD 24.90
- PolyPhen-2 0.08
- SIFT 0.02
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- MAPK1 VRT-11E: score 6.09