N29N (p.Asn29Asn) variant of MYPN (Myopalladin)
N29N (p.Asn29Asn) in MYPN (Myopalladin) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data, published literature, and structural context.
N29N (p.Asn29Asn) variant details
- p.Asn29Asn
- gnomAD 10-68121525-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.326
- CADD 7.14
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available
- Literature evidence available