N13S (p.Asn13Ser) variant of ABCD1 (P33897)
N13S (p.Asn13Ser) in ABCD1 (P33897) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data, published literature, and structural context.
N13S (p.Asn13Ser) variant details
- p.Asn13Ser
- gnomAD X-153725304-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.364
- REVEL 0.29
- CADD 0.26
- PolyPhen-2 0.00
- SIFT 0.99
- Population evidence available
- Structural context available
- Literature evidence available