L15F (p.Leu15Phe) variant of PRKAR1A (P10644)
L15F (p.Leu15Phe) 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; Carney complex, type 1. The record also includes structural context.
L15F (p.Leu15Phe) variant details
- p.Leu15Phe
- NCI-TCGA Cosmic COSV6223
- cosmic curated COSV62235
- Uncertain significance
- Hereditary cancer-predisposing syndrome; Carney complex, type 1
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome; Carney complex, type 1)
- UniProt: Uncertain significance
- Structural context available