List of variants in gene combination FLNC, LOC129999273 reported as likely benign for hereditary skeletal muscle disorder

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: 14

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001458.5(FLNC):c.2125G>A (p.Ala709Thr)	rs192725607	0.00053
NM_001458.5(FLNC):c.2128G>A (p.Asp710Asn)	rs370035829	0.00020
NM_001458.5(FLNC):c.2139C>G (p.Pro713=)	rs746825094	0.00004
NM_001458.5(FLNC):c.2124C>T (p.Asp708=)	rs187481700	0.00003
NM_001458.5(FLNC):c.2130C>T (p.Asp710=)	rs778781499	0.00003
NM_001458.5(FLNC):c.2127C>T (p.Ala709=)	rs753225379	0.00001
NM_001458.5(FLNC):c.2122-12dup
NM_001458.5(FLNC):c.2122-18C>T
NM_001458.5(FLNC):c.2122-9T>C	rs369054931
NM_001458.5(FLNC):c.2140A>G (p.Ile714Val)
NM_001458.5(FLNC):c.2142C>A (p.Ile714=)	rs199595235
NM_001458.5(FLNC):c.2142C>T (p.Ile714=)	rs199595235
NM_001458.5(FLNC):c.2145C>T (p.Asp715=)	rs1585157201
NM_001458.5(FLNC):c.2151G>A (p.Lys717=)

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.