A77G (p.Ala77Gly) variant of SLC40A1 (Ferroportin)
A77G (p.Ala77Gly) in SLC40A1 (Ferroportin) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact in the context of in HFE4. The record also includes structural context.
A77G (p.Ala77Gly) variant details
- p.Ala77Gly
- NCI-TCGA Cosmic COSV5372
- Variant assessed as somatic; moderate impact.
- in HFE4
- Missense
- UniProt: Variant assessed as somatic; moderate impact. (in HFE4)
- Structural context available