V18G (p.Val18Gly) variant of GATA3 (P23771)
V18G (p.Val18Gly) in GATA3 (P23771) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The record also includes structural context.
V18G (p.Val18Gly) variant details
- p.Val18Gly
- rs985445864
- ClinGen CA375965012
- ClinVar RCV000722481
- TOPMed rs985445864
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available