E37K (p.Glu37Lys) variant of CNTNAP2 (Q9UHC6)
E37K (p.Glu37Lys) 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.
E37K (p.Glu37Lys) variant details
- p.Glu37Lys
- NCI-TCGA Cosmic COSV6215
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.48
- MetaSVM -0.07
- SIFT 0.02
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available