P37S (p.Pro37Ser) variant of PPARG (P37231)
P37S (p.Pro37Ser) in PPARG (P37231) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P37S (p.Pro37Ser) variant details
- p.Pro37Ser
- NCI-TCGA Cosmic COSV1043
- NCI-TCGA Cosmic COSV5514
- cosmic curated COSV55140
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available