L95P (p.Leu95Pro) variant of KRT17 (Keratin, type I cytoskeletal 17)
L95P (p.Leu95Pro) in KRT17 (Keratin, type I cytoskeletal 17) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as pathogenic in the context of not provided. The available variant effect predictions contribute to a CATVariant prioritization score of 0.95 / 1. The record also includes published literature and structural context.
L95P (p.Leu95Pro) variant details
- p.Leu95Pro
- rs28928899
- ClinGen CA216615
- ClinVar RCV000015700
- ClinVar RCV000056518
- Pathogenic
- not provided
- Missense
- Variant Prioritization Score for Impact Estimate 0.954
- AlphaMissense 1.00
- MetaLR 0.94
- MetaSVM 1.10
- PolyPhen-2 1.00
- SIFT 0.00
- EVE 0.92
- ClinVar: Pathogenic (not provided)
- EBI: Pathogenic (in PC2)
- UniProt: Pathogenic (in PC2)
- Structural context available
- Cited in: Novel and recurrent mutations in the genes encoding keratins K6a, K16 and K17 in 13 cases of pachyonychia congenita. (PMID 11886499)
- Cited in: Pachyonychia Congenita. (PMID 20301457)