T56N (p.Thr56Asn) variant of FSHR (P23945)
T56N (p.Thr56Asn) in FSHR (P23945) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
T56N (p.Thr56Asn) variant details
- p.Thr56Asn
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.52
- MetaSVM -0.08
- SIFT 0.06
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available