G37D (p.Gly37Asp) variant of HNF4A (P41235)
G37D (p.Gly37Asp) in HNF4A (P41235) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G37D (p.Gly37Asp) variant details
- p.Gly37Asp
- NCI-TCGA Cosmic COSV1002
- cosmic curated COSV10029
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available