Q167H (p.Gln167His) variant of PPARGC1A (Q9UBK2)
Q167H (p.Gln167His) 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.
Q167H (p.Gln167His) variant details
- p.Gln167His
- NCI-TCGA Cosmic COSV5352
- cosmic curated COSV53527
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available