Q41H (p.Gln41His) variant of FTO (Q9C0B1)
Q41H (p.Gln41His) in FTO (Q9C0B1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
Q41H (p.Gln41His) variant details
- p.Gln41His
- NCI-TCGA Cosmic COSV6711
- cosmic curated COSV67114
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available