R56I (p.Arg56Ile) variant of ETFDH (Q16134)
R56I (p.Arg56Ile) in ETFDH (Q16134) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R56I (p.Arg56Ile) variant details
- p.Arg56Ile
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available