List of variants in gene FLNB reported as likely benign for not specified

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: 43

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001457.4(FLNB):c.6956T>C (p.Ile2319Thr)	rs116826041	0.00739
NM_001457.4(FLNB):c.669G>A (p.Pro223=)	rs140815373	0.00527
NM_001457.4(FLNB):c.3240G>A (p.Pro1080=)	rs77989135	0.00333
NM_001457.4(FLNB):c.4222+19A>C	rs146229370	0.00319
NM_001457.4(FLNB):c.292+14C>G	rs200721532	0.00260
NM_001457.4(FLNB):c.4222+8A>G	rs190025781	0.00248
NM_001457.4(FLNB):c.1559C>T (p.Pro520Leu)	rs138220431	0.00247
NM_001457.4(FLNB):c.1472T>C (p.Met491Thr)	rs147575358	0.00203
NM_001457.4(FLNB):c.6231C>T (p.Asp2077=)	rs145280904	0.00184
NM_001457.4(FLNB):c.6683T>C (p.Ile2228Thr)	rs149629209	0.00148
NM_001457.4(FLNB):c.4929C>T (p.Ala1643=)	rs149070858	0.00140
NM_001457.4(FLNB):c.292+12G>C	rs201148582	0.00066
NM_001457.4(FLNB):c.4672-11A>G	rs72884428	0.00064
NM_001457.4(FLNB):c.7530G>A (p.Ser2510=)	rs141700862	0.00056
NM_001457.4(FLNB):c.1196A>G (p.Lys399Arg)	rs145673747	0.00043
NM_001457.4(FLNB):c.1704G>A (p.Ala568=)	rs139001948	0.00043
NM_001457.4(FLNB):c.3981G>A (p.Gln1327=)	rs201441533	0.00033
NM_001457.4(FLNB):c.3594G>A (p.Thr1198=)	rs143566075	0.00024
NM_001457.4(FLNB):c.5887+8A>G	rs143066905	0.00023
NM_001457.4(FLNB):c.1534G>A (p.Ala512Thr)	rs201544295	0.00022
NM_001457.4(FLNB):c.5445C>T (p.Tyr1815=)	rs755702006	0.00019
NM_001457.4(FLNB):c.5769C>T (p.Ala1923=)	rs201723447	0.00019
NM_001457.4(FLNB):c.7198+20C>G	rs201580886	0.00019
NM_001457.4(FLNB):c.4390+8T>A	rs377095569	0.00018
NM_001457.4(FLNB):c.3753T>C (p.Phe1251=)	rs751650356	0.00011
NM_001457.4(FLNB):c.762G>A (p.Pro254=)	rs371715057	0.00011
NM_001457.4(FLNB):c.4281C>T (p.Ala1427=)	rs188516921	0.00009
NM_001457.4(FLNB):c.6666C>T (p.Gly2222=)	rs144628013	0.00008
NM_001457.4(FLNB):c.7164C>T (p.Ser2388=)	rs757418085	0.00006
NM_001457.4(FLNB):c.4287C>T (p.Pro1429=)	rs376873981	0.00005
NM_001457.4(FLNB):c.2935G>A (p.Val979Met)	rs376511120	0.00004
NM_001457.4(FLNB):c.4671+5C>G	rs776434196	0.00004
NM_001457.4(FLNB):c.541+15C>T	rs770019318	0.00004
NM_001457.4(FLNB):c.246G>C (p.Val82=)	rs780155723	0.00002
NM_001457.4(FLNB):c.282C>T (p.Leu94=)	rs745493076	0.00001
NM_001457.4(FLNB):c.3835G>A (p.Glu1279Lys)	rs983695359	0.00001
NM_001457.4(FLNB):c.5181+17T>C	rs367874839	0.00001
NM_001457.4(FLNB):c.787+14C>T	rs1421148550	0.00001
NM_001457.4(FLNB):c.9A>G (p.Val3=)	rs199846967	0.00001
NM_001457.4(FLNB):c.2773G>T (p.Gly925Cys)	rs139875974
NM_001457.4(FLNB):c.4515-24GT[4]	rs151085835
NM_001457.4(FLNB):c.5037C>T (p.Ala1679=)	rs770779551
NM_001457.4(FLNB):c.7770A>G (p.Glu2590=)

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.