G32V (p.Gly32Val) variant of INS (Insulin)
G32V (p.Gly32Val) in INS (Insulin) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as likely pathogenic in the context of not provided. The record also includes structural context.
G32V (p.Gly32Val) variant details
- p.Gly32Val
- rs2133676747
- ClinGen CA379121802
- ClinVar RCV001817993
- Ensembl rs2133676747
- Likely pathogenic
- not provided
- Missense
- ClinVar: Likely pathogenic (not provided)
- EBI: Likely pathogenic (in PNDM4)
- UniProt: Likely pathogenic (in PNDM4)
- Structural context available