N13D (p.Asn13Asp) variant of ABCD1 (P33897)
N13D (p.Asn13Asp) in ABCD1 (P33897) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data, published literature, and structural context.
N13D (p.Asn13Asp) variant details
- p.Asn13Asp
- gnomAD X-153725303-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.318
- REVEL 0.13
- CADD 12.70
- PolyPhen-2 0.00
- SIFT 0.35
- Population evidence available
- Structural context available
- Literature evidence available