V56G (p.Val56Gly) variant of MAPK3 (P27361)
V56G (p.Val56Gly) in MAPK3 (P27361) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.72 / 1. The record also includes population frequency data and structural context.
V56G (p.Val56Gly) variant details
- p.Val56Gly
- gnomAD rs1157149769
- Missense
- Variant Prioritization Score for Impact Estimate 0.721
- REVEL 0.89
- CADD 28.90
- PolyPhen-2 0.95
- SIFT 0.00
- Most common in the Finnish in Finland (FIN) population (allele frequency 2.8e-05)
- Structural context available