N29S (p.Asn29Ser) variant of MYPN (Myopalladin)
N29S (p.Asn29Ser) in MYPN (Myopalladin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data, published literature, and structural context.
N29S (p.Asn29Ser) variant details
- p.Asn29Ser
- gnomAD 10-68121524-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.194
- REVEL 0.12
- CADD 18.70
- PolyPhen-2 0.02
- SIFT 0.16
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available
- Literature evidence available