N28D (p.Asn28Asp) variant of ACADM (P11310)
N28D (p.Asn28Asp) in ACADM (P11310) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data, published literature, and structural context.
N28D (p.Asn28Asp) variant details
- p.Asn28Asp
- gnomAD 1-75728452-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.106
- REVEL 0.14
- CADD 0.29
- PolyPhen-2 0.01
- SIFT 0.31
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)
- Structural context available
- Literature evidence available