F39V (p.Phe39Val) variant of ABCG2 (Q9UNQ0)
F39V (p.Phe39Val) in ABCG2 (Q9UNQ0) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not specified. The record also includes structural context.
F39V (p.Phe39Val) variant details
- p.Phe39Val
- rs2476286757
- ClinGen CA357634599
- ClinVar RCV004134620
- Uncertain significance
- not specified
- Missense
- ClinVar: Uncertain significance (not specified)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available