A49S (p.Ala49Ser) variant of ETFB (P38117)
A49S (p.Ala49Ser) in ETFB (P38117) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A49S (p.Ala49Ser) variant details
- p.Ala49Ser
- NCI-TCGA Cosmic COSV1004
- cosmic curated COSV10049
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available