List of variants in gene KRT14 reported by CeGaT Center for Human Genetics Tuebingen

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_000526.5(KRT14):c.166C>T (p.Arg56Cys)	rs117484558	0.00519
NM_000526.5(KRT14):c.88C>T (p.Arg30Cys)	rs201069984	0.00188
NM_000526.5(KRT14):c.1203G>A (p.Leu401=)	rs139804375	0.00054
NM_000526.5(KRT14):c.252T>C (p.Phe84=)	rs573807721	0.00003
NM_000526.5(KRT14):c.1003C>T (p.Arg335Trp)	rs765544134	0.00001
NM_000526.5(KRT14):c.1321+8C>A	rs1360694320	0.00001
NM_000526.5(KRT14):c.183A>G (p.Gly61=)
NM_000526.5(KRT14):c.355A>G (p.Met119Val)	rs61263401
NM_000526.5(KRT14):c.397G>A (p.Val133Met)	rs61027685
NM_000526.5(KRT14):c.40del (p.Ser13_Met14insTer)	rs1567738332
NM_000526.5(KRT14):c.566A>G (p.Gln189Arg)	rs748092575
NM_000526.5(KRT14):c.627C>T (p.Asn209=)
NM_000526.5(KRT14):c.815T>C (p.Met272Thr)	rs61371557

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