A14G (p.Ala14Gly) variant of CSF1R (P07333)
A14G (p.Ala14Gly) in CSF1R (P07333) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance.
A14G (p.Ala14Gly) variant details
- p.Ala14Gly
- ExAC rs774289908
- gnomAD rs774289908
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance