"Fulgent Genetics, Fulgent Genetics"[submitter] AND "KRT14"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 66319	NM_000526.5(KRT14):c.1237G>A (p.Ala413Thr)	KRT14 (A413T)	Single nucleotide variant (missense variant)	KRT14-related condition +7 more	GBenign/Likely benign
Select item 66346	NM_000526.5(KRT14):c.369T>C (p.Asn123=)	KRT14	Single nucleotide variant (synonymous variant)	not specified +7 more	GBenign
Select item 66332	NM_000526.5(KRT14):c.193C>T (p.Leu65=)	KRT14	Single nucleotide variant (synonymous variant)	not provided +7 more	GBenign
Select item 66331	NM_000526.5(KRT14):c.189C>T (p.Cys63=)	KRT14	Single nucleotide variant (synonymous variant)	not provided +7 more	GBenign
Select item 1668287	NM_000526.5(KRT14):c.188G>A (p.Cys63Tyr)	KRT14 (C63Y)	Single nucleotide variant (missense variant)	Dermatopathia pigmentosa reticularis +6 more	GBenign
Select item 781859	NM_000526.5(KRT14):c.166C>T (p.Arg56Cys)	KRT14 (R56C)	Single nucleotide variant (missense variant)	not provided +6 more	GBenign/Likely benign

ClinVar