K59T (p.Lys59Thr) variant of CDH2 (Cadherin-2)
K59T (p.Lys59Thr) in CDH2 (Cadherin-2) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data and structural context.
K59T (p.Lys59Thr) variant details
- p.Lys59Thr
- NCI-TCGA Cosmic COSV5229
- cosmic curated COSV52295
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.239
- REVEL 0.10
- MetaLR 0.07
- MetaSVM -1.07
- CADD 21.70
- PolyPhen-2 0.00
- SIFT 0.21
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the South Asian population (allele frequency 2.3e-05)
- Structural context available