N29K (p.Asn29Lys) variant of MYPN (Myopalladin)
N29K (p.Asn29Lys) 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.
N29K (p.Asn29Lys) variant details
- p.Asn29Lys
- Ensembl rs756617551
- Missense
- Variant Prioritization Score for Impact Estimate 0.198
- REVEL 0.06
- CADD 14.70
- PolyPhen-2 0.02
- SIFT 0.59
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available