P44T (p.Pro44Thr) variant of CNTNAP2 (Q9UHC6)
P44T (p.Pro44Thr) 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.
P44T (p.Pro44Thr) variant details
- p.Pro44Thr
- NCI-TCGA Cosmic COSV6217
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.87
- MetaSVM 0.72
- SIFT 0.01
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available