P16L (p.Pro16Leu) variant of CNGA1 (P29973)
P16L (p.Pro16Leu) 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.
P16L (p.Pro16Leu) variant details
- p.Pro16Leu
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available