S51L (p.Ser51Leu) variant of CNGA1 (P29973)
S51L (p.Ser51Leu) 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.
S51L (p.Ser51Leu) variant details
- p.Ser51Leu
- NCI-TCGA Cosmic COSV1006
- cosmic curated COSV10065
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available