V91D (p.Val91Asp) variant of PPARGC1A (Q9UBK2)
V91D (p.Val91Asp) 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.
V91D (p.Val91Asp) variant details
- p.Val91Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available