V189G (p.Val189Gly) variant of GJB1 (Gap junction beta-1 protein)
V189G (p.Val189Gly) in GJB1 (Gap junction beta-1 protein) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as pathogenic/likely pathogenic in the context of not provided; Charcot-Marie-Tooth Neuropathy X. The record also includes published literature and structural context.
V189G (p.Val189Gly) variant details
- p.Val189Gly
- rs1064794244
- ClinGen CA16621493
- ClinVar RCV000480241
- ClinVar RCV000789819
- Pathogenic/Likely pathogenic
- not provided; Charcot-Marie-Tooth Neuropathy X
- Missense
- ClinVar: Pathogenic/Likely pathogenic (not provided; Charcot-Marie-Tooth Neuropathy X)
- EBI: Pathogenic (in CMTX1)
- UniProt: Pathogenic (in CMTX1)
- Structural context available
- Cited in: Connexin32 and X-linked Charcot-Marie-Tooth disease. (PMID 9361298)
- Cited in: Charcot-Marie-Tooth Hereditary Neuropathy Overview. (PMID 20301532)