S10N (p.Ser10Asn) variant of FBXW7 (Q969H0)
S10N (p.Ser10Asn) in FBXW7 (Q969H0) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Inborn genetic diseases. The record also includes structural context.
S10N (p.Ser10Asn) variant details
- p.Ser10Asn
- Ensembl rs2126882888
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance
- Structural context available