List of variants in gene KRT5 reported as benign for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 27

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000424.4(KRT5):c.555+9C>T	rs638907	0.18403
NM_000424.4(KRT5):c.1582A>G (p.Ser528Gly)	rs11549950	0.17563
NM_000424.4(KRT5):c.1065A>C (p.Thr355=)	rs4761924	0.15330
NM_000424.4(KRT5):c.1474+163A>G	rs1799902	0.15326
NM_000424.4(KRT5):c.1627G>A (p.Gly543Ser)	rs11549949	0.15185
NM_000424.4(KRT5):c.351C>T (p.Leu117=)	rs11549951	0.07903
NM_000424.4(KRT5):c.413G>A (p.Gly138Glu)	rs11170164	0.05271
NM_000424.4(KRT5):c.142A>C (p.Arg48=)	rs61747180	0.01877
NM_000424.4(KRT5):c.259T>G (p.Phe87Val)	rs61747188	0.01764
NM_000424.4(KRT5):c.156G>A (p.Ala52=)	rs74093478	0.01559
NM_000424.4(KRT5):c.30G>A (p.Arg10=)	rs61747182	0.00780
NM_000424.4(KRT5):c.1071C>T (p.Ala357=)	rs149467228	0.00503
NM_000424.4(KRT5):c.1636C>A (p.Leu546Ile)	rs114734812	0.00394
NM_000424.4(KRT5):c.1555G>A (p.Gly519Ser)	rs140352947	0.00326
NM_000424.4(KRT5):c.1705G>A (p.Gly569Arg)	rs148276250	0.00253
NM_000424.4(KRT5):c.1475-6C>T	rs142320369	0.00105
NM_000424.4(KRT5):c.381C>T (p.Phe127=)	rs150390099	0.00069
NM_000424.4(KRT5):c.471C>T (p.Ile157=)	rs151258734	0.00019
NM_000424.4(KRT5):c.110G>A (p.Arg37Gln)	rs61747181	0.00018
NM_000424.4(KRT5):c.280G>A (p.Gly94Ser)	rs138806570	0.00009
NM_000424.4(KRT5):c.187C>T (p.Arg63Trp)	rs776667863	0.00008
NM_000424.4(KRT5):c.1536C>T (p.Leu512=)	rs148806544	0.00005
NM_000424.4(KRT5):c.57C>T (p.Thr19=)	rs529397720	0.00004
NM_000424.4(KRT5):c.86G>A (p.Arg29His)	rs543574061	0.00001
NM_000424.4(KRT5):c.1475-37A>T	rs28694819
NM_000424.4(KRT5):c.1554C>A (p.Gly518=)	rs144226740
NM_000424.4(KRT5):c.1620C>T (p.Val540=)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.