G2W (p.Gly2Trp) variant of ERCC5 (P28715)
G2W (p.Gly2Trp) in ERCC5 (P28715) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.83 / 1. The record also includes population frequency data.
G2W (p.Gly2Trp) variant details
- p.Gly2Trp
- TOPMed rs1178467021
- gnomAD rs1178467021
- Missense
- Variant Prioritization Score for Impact Estimate 0.832
- CADD 32.00
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)