P20T (p.Pro20Thr) variant of SMARCA4 (P51532)
P20T (p.Pro20Thr) in SMARCA4 (P51532) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
P20T (p.Pro20Thr) variant details
- p.Pro20Thr
- Ensembl rs2145721758
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available