G42V (p.Gly42Val) variant of KIT (P10721)
G42V (p.Gly42Val) in KIT (P10721) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
G42V (p.Gly42Val) variant details
- p.Gly42Val
- ExAC rs746856550
- gnomAD rs746856550
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available