V39M (p.Val39Met) variant of ETFDH (Q16134)
V39M (p.Val39Met) 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.
V39M (p.Val39Met) variant details
- p.Val39Met
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available