V139G (p.Val139Gly) variant of HNF1B (Hepatocyte nuclear factor 1-beta)
V139G (p.Val139Gly) in HNF1B (Hepatocyte nuclear factor 1-beta) 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.
V139G (p.Val139Gly) variant details
- p.Val139Gly
- rs2511829485
- ClinGen CA398751523
- ClinVar RCV003579993
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available