List of variants in gene KRT14 reported by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000526.5(KRT14):c.188G>A (p.Cys63Tyr)	rs6503640	0.99456
NM_000526.5(KRT14):c.193C>T (p.Leu65=)	rs3826551	0.58145
NM_000526.5(KRT14):c.189C>T (p.Cys63=)	rs11551758	0.56357
NM_000526.5(KRT14):c.369T>C (p.Asn123=)	rs3826549	0.56333
NM_000526.5(KRT14):c.1237G>A (p.Ala413Thr)	rs59780231	0.01556
NM_000526.5(KRT14):c.166C>T (p.Arg56Cys)	rs117484558	0.00519

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