C31G (p.Cys31Gly) variant of INS (Insulin)
C31G (p.Cys31Gly) in INS (Insulin) 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.
C31G (p.Cys31Gly) variant details
- p.Cys31Gly
- rs2133676771
- ClinGen CA379121819
- ClinVar RCV001864754
- Ensembl rs2133676771
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available