R67G (p.Arg67Gly) variant of MAPK3 (P27361)
R67G (p.Arg67Gly) in MAPK3 (P27361) 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 and structural context.
R67G (p.Arg67Gly) variant details
- p.Arg67Gly
- 1000Genomes rs567762331
- ExAC rs567762331
- TOPMed rs567762331
- gnomAD rs567762331
- Missense
- Variant Prioritization Score for Impact Estimate 0.56
- REVEL 0.54
- CADD 26.00
- PolyPhen-2 0.78
- SIFT 0.03
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available