M14I (p.Met14Ile) variant of KRT14 (Keratin, type I cytoskeletal 14)
M14I (p.Met14Ile) in KRT14 (Keratin, type I cytoskeletal 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 0.29 / 1. The record also includes population frequency data and structural context.
M14I (p.Met14Ile) variant details
- p.Met14Ile
- NCI-TCGA Cosmic COSV9939
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.293
- REVEL 0.18
- CADD 19.60
- PolyPhen-2 0.00
- SIFT 0.39
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9.1e-07)
- Structural context available