S15T (p.Ser15Thr) variant of GALT (P07902)
S15T (p.Ser15Thr) in GALT (P07902) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data and structural context.
S15T (p.Ser15Thr) variant details
- p.Ser15Thr
- ExAC rs756267534
- TOPMed rs756267534
- Missense
- Variant Prioritization Score for Impact Estimate 0.394
- REVEL 0.39
- CADD 10.80
- PolyPhen-2 0.01
- SIFT 0.50
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available