R16G (p.Arg16Gly) variant of MAPK3 (P27361)
R16G (p.Arg16Gly) in MAPK3 (P27361) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data and structural context.
R16G (p.Arg16Gly) variant details
- p.Arg16Gly
- TOPMed rs1314762868
- gnomAD rs1314762868
- Missense
- Variant Prioritization Score for Impact Estimate 0.24
- REVEL 0.16
- CADD 16.40
- PolyPhen-2 0.00
- SIFT 0.41
- Most common in the Non-Finnish European population (allele frequency 7.9e-06)
- Structural context available