A7V (p.Ala7Val) variant of PRKAR1A (P10644)
A7V (p.Ala7Val) 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.
A7V (p.Ala7Val) variant details
- p.Ala7Val
- cosmic curated COSV10943
- NCI-TCGA TCGA novel
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available