D4G (p.Asp4Gly) variant of MYPN (Myopalladin)
D4G (p.Asp4Gly) in MYPN (Myopalladin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data and structural context.
D4G (p.Asp4Gly) variant details
- p.Asp4Gly
- TOPMed rs1197594190
- gnomAD rs1197594190
- Missense
- Variant Prioritization Score for Impact Estimate 0.358
- REVEL 0.18
- CADD 23.10
- PolyPhen-2 0.11
- SIFT 0.09
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available