A61P (p.Ala61Pro) variant of HNF4A (P41235)
A61P (p.Ala61Pro) 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.
A61P (p.Ala61Pro) variant details
- p.Ala61Pro
- NCI-TCGA Cosmic COSV5738
- cosmic curated COSV57383
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available