P44L (p.Pro44Leu) variant of CNTNAP2 (Q9UHC6)
P44L (p.Pro44Leu) in CNTNAP2 (Q9UHC6) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P44L (p.Pro44Leu) variant details
- p.Pro44Leu
- NCI-TCGA Cosmic COSV6216
- NCI-TCGA Cosmic COSV6226
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available