T36S (p.Thr36Ser) variant of PTCH1 (Protein patched homolog 1)
T36S (p.Thr36Ser) in PTCH1 (Protein patched homolog 1) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
T36S (p.Thr36Ser) variant details
- p.Thr36Ser
- gnomAD rs1843898216
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available