S42G (p.Ser42Gly) variant of EDN1 (Endothelin-1)
S42G (p.Ser42Gly) in EDN1 (Endothelin-1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S42G (p.Ser42Gly) variant details
- p.Ser42Gly
- NCI-TCGA Cosmic COSV6508
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available