P38Q (p.Pro38Gln) variant of CNTNAP2 (Q9UHC6)
P38Q (p.Pro38Gln) 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.
P38Q (p.Pro38Gln) variant details
- p.Pro38Gln
- NCI-TCGA Cosmic COSV1006
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available