List of variants in gene FLNC reported by Phosphorus, Inc.

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

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001458.5(FLNC):c.7947C>T (p.Phe2649=)	rs368849358	0.00083
NM_001458.5(FLNC):c.6175G>A (p.Val2059Met)	rs201333104	0.00076
NM_001458.5(FLNC):c.4140C>T (p.Thr1380=)	rs183668401	0.00004
NM_001458.5(FLNC):c.6864C>T (p.Val2288=)	rs761269440	0.00004
NM_001458.5(FLNC):c.4413A>T (p.Gln1471His)	rs765435961	0.00003
NM_001458.5(FLNC):c.4061G>A (p.Arg1354Gln)	rs572132215	0.00002
NM_001458.5(FLNC):c.4134G>A (p.Ala1378=)	rs200942470	0.00001
NM_001458.5(FLNC):c.4576C>T (p.Arg1526Cys)	rs746275035	0.00001
NM_001458.5(FLNC):c.5670G>A (p.Gly1890=)	rs369881758	0.00001
NM_001458.5(FLNC):c.6123C>T (p.Ala2041=)	rs769675272	0.00001
NM_001458.5(FLNC):c.3135C>A (p.His1045Gln)	rs988307328
NM_001458.5(FLNC):c.4566G>T (p.Gln1522His)	rs559667295
NM_001458.5(FLNC):c.7596T>A (p.Asn2532Lys)	rs377522797

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.