G53G (p.Gly53Gly) variant of MYPN (Myopalladin)
G53G (p.Gly53Gly) in MYPN (Myopalladin) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data, published literature, and structural context.
G53G (p.Gly53Gly) variant details
- p.Gly53Gly
- gnomAD 10-68121597-A-G
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.125
- CADD 6.29
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available