C9G (p.Cys9Gly) variant of ACADM (P11310)
C9G (p.Cys9Gly) in ACADM (P11310) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.50 / 1. The record also includes population frequency data, published literature, and structural context.
C9G (p.Cys9Gly) variant details
- p.Cys9Gly
- gnomAD 1-75728389-T-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.505
- CADD 20.80
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)
- Structural context available
- Literature evidence available