Y13D (p.Tyr13Asp) variant of ETFDH (Q16134)
Y13D (p.Tyr13Asp) 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.
Y13D (p.Tyr13Asp) variant details
- p.Tyr13Asp
- NCI-TCGA Cosmic COSV1003
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available