T41N (p.Thr41Asn) variant of PPARG (P37231)
T41N (p.Thr41Asn) 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.
T41N (p.Thr41Asn) variant details
- p.Thr41Asn
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available