G1118C (p.Gly1118Cys) variant of ATP7A (Copper-transporting ATPase 1)
G1118C (p.Gly1118Cys) in ATP7A (Copper-transporting ATPase 1) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as likely pathogenic in the context of Menkes kinky-hair syndrome. The available variant effect predictions contribute to a CATVariant prioritization score of 0.92 / 1. The record also includes published literature.
G1118C (p.Gly1118Cys) variant details
- p.Gly1118Cys
- rs797045376
- ClinGen CA277364
- ClinVar RCV000194716
- Ensembl rs797045376
- Likely pathogenic
- Menkes kinky-hair syndrome
- Missense
- Variant Prioritization Score for Impact Estimate 0.916
- AlphaMissense 0.99
- MetaLR 0.90
- MetaSVM 1.05
- PolyPhen-2 1.00
- SIFT 0.00
- EVE 0.85
- ClinVar: Likely pathogenic (Menkes kinky-hair syndrome)
- EBI: Likely pathogenic (in MNK)
- UniProt: Likely pathogenic (in MNK)
- Cited in: ATP7A-Related Copper Transport Disorders. (PMID 20301586)
- Cited in: Clinical utility gene card for: Menkes disease. (PMID 21487442)