F86S (p.Phe86Ser) variant of CNGA1 (P29973)
F86S (p.Phe86Ser) in CNGA1 (P29973) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
F86S (p.Phe86Ser) variant details
- p.Phe86Ser
- NCI-TCGA Cosmic COSV6205
- cosmic curated COSV62054
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available