W41R (p.Trp41Arg) variant of GALT (P07902)
W41R (p.Trp41Arg) in GALT (P07902) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.85 / 1. The record also includes population frequency data and structural context.
W41R (p.Trp41Arg) variant details
- p.Trp41Arg
- gnomAD rs1450493685
- Missense
- Variant Prioritization Score for Impact Estimate 0.848
- REVEL 0.96
- CADD 32.00
- PolyPhen-2 0.96
- SIFT 0.00
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available