P38T (p.Pro38Thr) variant of CNTNAP2 (Q9UHC6)
P38T (p.Pro38Thr) in CNTNAP2 (Q9UHC6) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
P38T (p.Pro38Thr) variant details
- p.Pro38Thr
- NCI-TCGA Cosmic COSV1006
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.65
- MetaSVM 0.33
- SIFT 0.19
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available