G56R (p.Gly56Arg) variant of MYPN (Myopalladin)
G56R (p.Gly56Arg) in MYPN (Myopalladin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data and structural context.
G56R (p.Gly56Arg) variant details
- p.Gly56Arg
- 1000Genomes rs189718354
- ExAC rs189718354
- gnomAD rs189718354
- Missense
- Variant Prioritization Score for Impact Estimate 0.204
- REVEL 0.04
- CADD 22.50
- PolyPhen-2 0.22
- SIFT 0.00
- Most common in the 1KG:GBR population (allele frequency 0.0057)
- Structural context available