G49G (p.Gly49Gly) variant of MYPN (Myopalladin)
G49G (p.Gly49Gly) in MYPN (Myopalladin) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data, published literature, and structural context.
G49G (p.Gly49Gly) variant details
- p.Gly49Gly
- rs1286172264
- gnomAD 10-68121585-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.163
- CADD 6.68
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available
- Literature evidence available