{{Rsnum
|rsid=4261597
|Gene=KRT10
|Chromosome=17
|position=40822284
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=T
|GMAF=0.001837
|Gene_s=KRT10,TMEM99
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{Venter SNP
|rsid=4261597
|allele=C
|frequency=
|uid=1103645323282
|type=homozygous_SNP
|hugo=KRT10
|ensembl gene=ENSG00000186395
|ensembl transcript=ENST00000269576
|sift=TOLERATED
|disease=Defects in KRT10 are a cause of annular epidermolytic ichthyosis (AEI) (MIM:607602); also known as cyclic ichthyosis with epidermolytic hyperkeratosis. AEI resembles clinical and histologic features of both epidermolytic hyperkeratosis and ichthyosis bullosa of Siemens.
}}

{{GET Evidence
|gene=KRT10
|aa_change=Ile101Ser
|aa_change_short=I101S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs4261597
|overall_frequency_n=10742
|overall_frequency_d=10758
|overall_frequency=0.998513
|n_genomes=56
|n_genomes_annotated=0
|n_haplomes=112
|n_articles=0
|n_articles_annotated=0
|qualityscore_in_silico=2
|qualitycomment_in_silico=Y
|gene_in_genetests=Y
|genetests_testable=Y
|nblosum100=5
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}