T21M (p.Thr21Met) variant of CLDN14 (Claudin-14)
T21M (p.Thr21Met) in CLDN14 (Claudin-14) 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 0.71 / 1. The record also includes population frequency data and structural context.
T21M (p.Thr21Met) variant details
- p.Thr21Met
- rs532176130
- NCI-TCGA Cosmic COSV1005
- cosmic curated COSV10057
- 1000Genomes rs532176130
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.707
- REVEL 0.74
- CADD 25.50
- PolyPhen-2 1.00
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available