G28R (p.Gly28Arg) variant of MYPN (Myopalladin)
G28R (p.Gly28Arg) in MYPN (Myopalladin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data and structural context.
G28R (p.Gly28Arg) variant details
- p.Gly28Arg
- ExAC rs748805804
- gnomAD rs748805804
- Missense
- Variant Prioritization Score for Impact Estimate 0.397
- REVEL 0.15
- CADD 22.60
- PolyPhen-2 0.09
- SIFT 1.00
- Most common in the South Asian population (allele frequency 2.3e-05)
- Structural context available