D39Y (p.Asp39Tyr) variant of GALT (P07902)
D39Y (p.Asp39Tyr) in GALT (P07902) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.81 / 1. The record also includes population frequency data and structural context.
D39Y (p.Asp39Tyr) variant details
- p.Asp39Tyr
- TOPMed rs1324892935
- gnomAD rs1324892935
- Missense
- Variant Prioritization Score for Impact Estimate 0.809
- REVEL 0.93
- CADD 32.00
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available