T118A (p.Thr118Ala) variant of PPARGC1A (Q9UBK2)
T118A (p.Thr118Ala) 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.
T118A (p.Thr118Ala) variant details
- p.Thr118Ala
- NCI-TCGA Cosmic COSV9933
- cosmic curated COSV99337
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available