R29G (p.Arg29Gly) variant of ACADM (P11310)
R29G (p.Arg29Gly) in ACADM (P11310) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data, published literature, and structural context.
R29G (p.Arg29Gly) variant details
- p.Arg29Gly
- gnomAD 1-75728455-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.277
- REVEL 0.32
- CADD 5.74
- PolyPhen-2 0.00
- SIFT 0.39
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available
- Literature evidence available