List of variants in gene FKBP14 reported by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_017946.4(FKBP14):c.525G>T (p.Val175=)	rs747381671	0.00014
NM_017946.4(FKBP14):c.246G>A (p.Leu82=)	rs188844900	0.00008
NM_017946.4(FKBP14):c.249G>T (p.Glu83Asp)
NM_017946.4(FKBP14):c.362dup (p.Glu122fs)	rs542489955
NM_017946.4(FKBP14):c.467_468del (p.Leu155_Ser156insTer)	rs753775062
NM_017946.4(FKBP14):c.52_55del (p.Ile18fs)	rs775594340
NM_017946.4(FKBP14):c.539_540delinsCA (p.His180Pro)
NM_017946.4(FKBP14):c.590G>C (p.Gly197Ala)
NM_017946.4(FKBP14):c.6G>T (p.Arg2Ser)	rs2127950957
NM_017946.4(FKBP14):c.86T>C (p.Ile29Thr)

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.