A18V (p.Ala18Val) variant of ETFDH (Q16134)
A18V (p.Ala18Val) 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.
A18V (p.Ala18Val) variant details
- p.Ala18Val
- NCI-TCGA Cosmic COSV5701
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available