List of variants in gene FLNB reported as benign by Eurofins NTD LLC (GA)

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: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001457.4(FLNB):c.3469G>A (p.Asp1157Asn)	rs1131356	0.33365
NM_001457.4(FLNB):c.6956T>C (p.Ile2319Thr)	rs116826041	0.00739
NM_001457.4(FLNB):c.720C>T (p.Ala240=)	rs111433950	0.00554
NM_001457.4(FLNB):c.4872C>T (p.Ile1624=)	rs147426569	0.00436
NM_001457.4(FLNB):c.3090C>T (p.Tyr1030=)	rs112968165	0.00406
NM_001457.4(FLNB):c.2382C>T (p.Asp794=)	rs146159035	0.00360
NM_001457.4(FLNB):c.3264C>T (p.Ser1088=)	rs112864468	0.00322
NM_001457.4(FLNB):c.362A>T (p.Tyr121Phe)	rs147846832	0.00269
NM_001457.4(FLNB):c.1044C>T (p.Asp348=)	rs111996979	0.00252
NM_001457.4(FLNB):c.6684C>T (p.Ile2228=)	rs138416613	0.00170
NM_001457.4(FLNB):c.6642C>T (p.Phe2214=)	rs140786324	0.00161

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.