{{Rsnum
|rsid=60399023
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=KRT14
|position=41586462
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KRT14
}}{{omim
|id=148066
|rsnum=60399023
|variant=0002
}}

{{ClinVar
|rsid=60399023
|Reversed=1
|FwdREF=C
|FwdALT=G,T
|REF=G
|ALT=A,C
|RSPOS=39742714
|CHROM=17
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=KRT14:3861
|GENE_NAME=KRT14
|GENE_ID=3861
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000017.10:g.39742714G>A; NC_000017.10:g.39742714G>C
|CLNSRC=Epithelial Biology; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=KRT14:c.373C>T; NBK1369; 148066.0002; KRT14:c.373C>G
|CLNSIG=5
|CLNCUI=C0079295; C0079295,.
|CLNDBN=Epidermolysis bullosa herpetiformis, Dowling-Meara; not provided
|Disease=Epidermolysis bullosa herpetiformis; not provided
|CLNACC=RCV000015716.21; RCV000056717.1; RCV000056716.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1369:C0079295:131760:79396
}}

{{PMID Auto
|PMID=1717157
|Title=Point mutations in human keratin 14 genes of epidermolysis bullosa simplex patients: genetic and functional analyses.
}}

{{PMID Auto
|PMID=10583131
|Title=A recurrent keratin 14 mutation in Dowling-Meara epidermolysis bullosa simplex.
}}

{{PMID Auto
|PMID=11331879
|Title=A 'hot-spot' mutation alters the mechanical properties of keratin filament networks.
}}

{{on chip | 23andMe v3}}