S14I (p.Ser14Ile) variant of CLDN14 (Claudin-14)
S14I (p.Ser14Ile) 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 0.63 / 1. The record also includes population frequency data and structural context.
S14I (p.Ser14Ile) variant details
- p.Ser14Ile
- NCI-TCGA Cosmic COSV5977
- cosmic curated COSV59771
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.628
- REVEL 0.61
- CADD 24.60
- PolyPhen-2 0.63
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available