N26S (p.Asn26Ser) variant of PRKAR1A (P10644)
N26S (p.Asn26Ser) in PRKAR1A (P10644) 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.
N26S (p.Asn26Ser) variant details
- p.Asn26Ser
- cosmic curated COSV10067
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available