A26G (p.Ala26Gly) variant of ABCD1 (P33897)
A26G (p.Ala26Gly) in ABCD1 (P33897) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.58 / 1. The record also includes population frequency data, published literature, and structural context.
A26G (p.Ala26Gly) variant details
- p.Ala26Gly
- gnomAD X-153725343-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.577
- REVEL 0.52
- CADD 22.70
- PolyPhen-2 0.27
- SIFT 0.00
- Population evidence available
- Structural context available
- Literature evidence available