R13G (p.Arg13Gly) variant of ACADM (P11310)
R13G (p.Arg13Gly) in ACADM (P11310) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.59 / 1. The record also includes population frequency data, published literature, and structural context.
R13G (p.Arg13Gly) variant details
- p.Arg13Gly
- gnomAD 1-75728407-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.585
- REVEL 0.58
- CADD 23.10
- PolyPhen-2 0.01
- SIFT 0.06
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available