S16* (p.Ser16Ter) variant of FSHR (P23945)
S16* (p.Ser16Ter) in FSHR (P23945) is a protein-truncating change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
S16* (p.Ser16Ter) variant details
- p.Ser16Ter
- NCI-TCGA Cosmic COSV1004
- cosmic curated COSV10043
- TOPMed rs983007484
- Variant assessed as somatic; high impact.
- Stop Gained
- UniProt: Variant assessed as somatic; high impact.
- Structural context available