R29G (p.Arg29Gly) variant of CHEK1 (O14757)
R29G (p.Arg29Gly) in CHEK1 (O14757) 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.
R29G (p.Arg29Gly) variant details
- p.Arg29Gly
- rs1555067411
- ClinGen CA383190150
- ClinVar RCV000586016
- Ensembl rs1555067411
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available