R25W (p.Arg25Trp) variant of GALT (P07902)
R25W (p.Arg25Trp) in GALT (P07902) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.58 / 1. The record also includes population frequency data and structural context.
R25W (p.Arg25Trp) variant details
- p.Arg25Trp
- gnomAD rs1821112297
- Missense
- Variant Prioritization Score for Impact Estimate 0.584
- REVEL 0.63
- CADD 26.40
- PolyPhen-2 0.77
- SIFT 0.00
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available