S39C (p.Ser39Cys) variant of PPARGC1A (Q9UBK2)
S39C (p.Ser39Cys) in PPARGC1A (Q9UBK2) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S39C (p.Ser39Cys) variant details
- p.Ser39Cys
- NCI-TCGA Cosmic COSV5352
- cosmic curated COSV53526
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available