D97E (p.Asp97Glu) variant of PPARGC1A (Q9UBK2)
D97E (p.Asp97Glu) in PPARGC1A (Q9UBK2) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
D97E (p.Asp97Glu) variant details
- p.Asp97Glu
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available