S42C (p.Ser42Cys) variant of GJB1 (Gap junction beta-1 protein)
S42C (p.Ser42Cys) in GJB1 (Gap junction beta-1 protein) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as likely pathogenic in the context of Charcot-Marie-Tooth disease X-linked dominant 1. The record also includes published literature and structural context.
S42C (p.Ser42Cys) variant details
- p.Ser42Cys
- rs1602348801
- ClinGen CA413501016
- ClinVar RCV000789795
- ClinVar RCV002249493
- Likely pathogenic
- Charcot-Marie-Tooth disease X-linked dominant 1
- Missense
- ClinVar: Likely pathogenic (Charcot-Marie-Tooth disease X-linked dominant 1)
- EBI: Likely pathogenic
- UniProt: Likely pathogenic
- Structural context available
- Cited in: Charcot-Marie-Tooth Hereditary Neuropathy Overview. (PMID 20301532)
- Cited in: GJB1 Disorders: Charcot-Marie-Tooth Neuropathy (CMT1X) and Central Nervous System Phenotypes. (PMID 20301548)