V38G (p.Val38Gly) variant of ERCC3 (P19447)
V38G (p.Val38Gly) in ERCC3 (P19447) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes structural context.
V38G (p.Val38Gly) variant details
- p.Val38Gly
- TOPMed rs1685356393
- Missense
- Variant Prioritization Score for Impact Estimate 0.223
- ESM-1b 0.00
- AlphaMissense 0.54
- Structural context available