P9S (p.Pro9Ser) variant of ABCD1 (P33897)
P9S (p.Pro9Ser) in ABCD1 (P33897) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data, published literature, and structural context.
P9S (p.Pro9Ser) variant details
- p.Pro9Ser
- gnomAD X-153725291-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.191
- REVEL 0.29
- CADD 0.14
- PolyPhen-2 0.00
- SIFT 0.38
- Population evidence available
- Structural context available
- Literature evidence available