V13G (p.Val13Gly) variant of GJB1 (Gap junction beta-1 protein)
V13G (p.Val13Gly) in GJB1 (Gap junction beta-1 protein) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Charcot-Marie-Tooth Neuropathy X. The record also includes published literature and structural context.
V13G (p.Val13Gly) variant details
- p.Val13Gly
- rs1220424626
- ClinGen CA413499483
- ClinVar RCV001319438
- gnomAD rs1220424626
- Uncertain significance
- Charcot-Marie-Tooth Neuropathy X
- Missense
- ClinVar: Uncertain significance (Charcot-Marie-Tooth Neuropathy X)
- EBI: Variant of uncertain significance (in CMTX1)
- UniProt: Uncertain significance (in CMTX1)
- Structural context available
- Cited in: Charcot-Marie-Tooth Hereditary Neuropathy Overview. (PMID 20301532)