C42C (p.Cys42Cys) variant of MYPN (Myopalladin)
C42C (p.Cys42Cys) in MYPN (Myopalladin) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data, published literature, and structural context.
C42C (p.Cys42Cys) variant details
- p.Cys42Cys
- gnomAD 10-68121564-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.206
- CADD 8.34
- Most common in the East Asian population (allele frequency 5e-05)
- Structural context available
- Literature evidence available