Y35C (p.Tyr35Cys) variant of SDHAF2 (Q9NX18)
Y35C (p.Tyr35Cys) in SDHAF2 (Q9NX18) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
Y35C (p.Tyr35Cys) variant details
- p.Tyr35Cys
- TOPMed rs1330914865
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available