S4Q (p.Ser4Gln) variant of HNF4A (P41235)
S4Q (p.Ser4Gln) in HNF4A (P41235) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
S4Q (p.Ser4Gln) variant details
- p.Ser4Gln
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available