N69N (p.Asn69Asn) variant of MYLK (Q15746)
N69N (p.Asn69Asn) in MYLK (Q15746) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data, published literature, and structural context.
N69N (p.Asn69Asn) variant details
- p.Asn69Asn
- rs2057590562
- gnomAD 3-123617789-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.132
- CADD 4.24
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available
- Literature evidence available