ClinVar Miner

Variants in gene FLNB with conflicting interpretations

Y axis minimum submission review status: Y axis collection method:
X axis minimum submission review status: X axis collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than two submissions, it may have multiple conflicts and therefore be counted in more than one conflict column. If this is the case, the "Variants with any kind of conflict" cell will be less than the sum of the conflicted variants cells to its left.

Variants with only 1 submission per condition Variants with at least 2 submissions on the same condition and no conflicts Variants with a synonymous conflict
(e.g. benign vs non-pathogenic)
Variants with a confidence conflict
(e.g. benign vs likely benign)
Variants with a benign or likely benign vs uncertain conflict Variants with a category conflict
(e.g. benign vs affects)
Variants with a clinically significant conflict
(e.g. benign vs pathogenic)
Variants with any conflict
412 68 8 42 38 0 0 84

Significance breakdown #

In the table below, cells that correspond to a term paired with itself represent synonymous conflicts, i.e. variants that have been annotated with different terms that map to the same standard term. To compare the terms that were actually submitted, check the box in the filters section at the top of this page.

pathogenic likely pathogenic uncertain significance likely benign benign
pathogenic 8 1 0 0 0
likely pathogenic 1 0 0 0 0
uncertain significance 0 0 0 32 9
likely benign 0 0 32 0 41
benign 0 0 9 41 0

All variants with conflicting interpretations #

Total variants: 84
Download table as spreadsheet
HGVS dbSNP
NM_001457.4(FLNB):c.1044C>T (p.Asp348=) rs111996979
NM_001457.4(FLNB):c.107G>A (p.Arg36His) rs142568031
NM_001457.4(FLNB):c.1196A>G (p.Lys399Arg) rs145673747
NM_001457.4(FLNB):c.1278C>T (p.His426=) rs572259451
NM_001457.4(FLNB):c.1327G>C (p.Val443Leu) rs200902568
NM_001457.4(FLNB):c.1534G>A (p.Ala512Thr) rs201544295
NM_001457.4(FLNB):c.1559C>T (p.Pro520Leu) rs138220431
NM_001457.4(FLNB):c.1704G>A (p.Ala568=) rs139001948
NM_001457.4(FLNB):c.1868A>T (p.Asp623Val) rs145314043
NM_001457.4(FLNB):c.1919C>T (p.Thr640Met) rs62621999
NM_001457.4(FLNB):c.1945C>T (p.Arg649Ter) rs80356517
NM_001457.4(FLNB):c.1946G>A (p.Arg649Gln) rs145910735
NM_001457.4(FLNB):c.2136G>A (p.Lys712=) rs777288340
NM_001457.4(FLNB):c.2382C>T (p.Asp794=) rs146159035
NM_001457.4(FLNB):c.2452C>T (p.Arg818Ter) rs80356519
NM_001457.4(FLNB):c.2453G>A (p.Arg818Gln) rs151259375
NM_001457.4(FLNB):c.2493C>T (p.Pro831=) rs145952210
NM_001457.4(FLNB):c.2494G>A (p.Ala832Thr) rs114804033
NM_001457.4(FLNB):c.274A>G (p.Ile92Val) rs62622011
NM_001457.4(FLNB):c.2773G>T (p.Gly925Cys) rs139875974
NM_001457.4(FLNB):c.2931G>A (p.Leu977=) rs574484752
NM_001457.4(FLNB):c.3090C>T (p.Tyr1030=) rs112968165
NM_001457.4(FLNB):c.3163G>A (p.Val1055Met) rs9813235
NM_001457.4(FLNB):c.3240G>A (p.Pro1080=) rs77989135
NM_001457.4(FLNB):c.3264C>T (p.Ser1088=) rs112864468
NM_001457.4(FLNB):c.3288C>T (p.Ser1096=) rs77934864
NM_001457.4(FLNB):c.3522G>A (p.Ser1174=) rs140993979
NM_001457.4(FLNB):c.3594G>A (p.Thr1198=) rs143566075
NM_001457.4(FLNB):c.362A>T (p.Tyr121Phe) rs147846832
NM_001457.4(FLNB):c.3724+36del rs56147140
NM_001457.4(FLNB):c.3753T>C (p.Phe1251=) rs751650356
NM_001457.4(FLNB):c.3771G>A (p.Pro1257=) rs146851485
NM_001457.4(FLNB):c.3785G>C (p.Gly1262Ala) rs111330368
NM_001457.4(FLNB):c.420G>A (p.Thr140=) rs192491895
NM_001457.4(FLNB):c.4222+8A>G rs190025781
NM_001457.4(FLNB):c.4233C>G (p.Phe1411Leu) rs143831841
NM_001457.4(FLNB):c.4307G>A (p.Arg1436Gln) rs140018418
NM_001457.4(FLNB):c.4362G>A (p.Pro1454=) rs150844992
NM_001457.4(FLNB):c.4362G>C (p.Pro1454=) rs150844992
NM_001457.4(FLNB):c.4377T>C (p.Val1459=) rs149921907
NM_001457.4(FLNB):c.4390+8T>A rs377095569
NM_001457.4(FLNB):c.4495G>A (p.Asp1499Asn) rs150445941
NM_001457.4(FLNB):c.4590T>C (p.Tyr1530=) rs141477764
NM_001457.4(FLNB):c.4671+11G>A rs115346578
NM_001457.4(FLNB):c.4756G>A (p.Gly1586Arg) rs80356513
NM_001457.4(FLNB):c.4819C>T (p.Arg1607Ter) rs80356520
NM_001457.4(FLNB):c.482T>G (p.Phe161Cys) rs80356506
NM_001457.4(FLNB):c.4872C>T (p.Ile1624=) rs147426569
NM_001457.4(FLNB):c.5071G>A (p.Gly1691Ser) rs80356503
NM_001457.4(FLNB):c.5220C>T (p.Asn1740=) rs531970315
NM_001457.4(FLNB):c.5445C>T (p.Tyr1815=) rs755702006
NM_001457.4(FLNB):c.5646G>A (p.Pro1882=) rs114882667
NM_001457.4(FLNB):c.5769C>T (p.Ala1923=) rs201723447
NM_001457.4(FLNB):c.5785G>A (p.Asp1929Asn) rs146685642
NM_001457.4(FLNB):c.5887+8A>G rs143066905
NM_001457.4(FLNB):c.5916C>T (p.Gly1972=) rs112942586
NM_001457.4(FLNB):c.6000T>C (p.Gly2000=) rs140926445
NM_001457.4(FLNB):c.6003C>T (p.Asp2001=) rs184065600
NM_001457.4(FLNB):c.6017A>G (p.Lys2006Arg) rs62621996
NM_001457.4(FLNB):c.6028C>T (p.Arg2010Cys) rs138034708
NM_001457.4(FLNB):c.6047G>A (p.Arg2016Gln) rs137885421
NM_001457.4(FLNB):c.6154C>T (p.Leu2052=) rs372726521
NM_001457.4(FLNB):c.6173A>G (p.Lys2058Arg) rs141698427
NM_001457.4(FLNB):c.6210C>T (p.Ile2070=) rs538937637
NM_001457.4(FLNB):c.6231C>T (p.Asp2077=) rs145280904
NM_001457.4(FLNB):c.6408del (p.Ser2137fs) rs80356521
NM_001457.4(FLNB):c.6642C>T (p.Phe2214=) rs140786324
NM_001457.4(FLNB):c.6666C>T (p.Gly2222=) rs144628013
NM_001457.4(FLNB):c.6680C>G (p.Ser2227Cys) rs138327769
NM_001457.4(FLNB):c.6684C>T (p.Ile2228=) rs138416613
NM_001457.4(FLNB):c.669G>A (p.Pro223=) rs140815373
NM_001457.4(FLNB):c.6741G>A (p.Ser2247=) rs143400214
NM_001457.4(FLNB):c.679G>A (p.Glu227Lys) rs80356508
NM_001457.4(FLNB):c.6843C>T (p.Ile2281=) rs140332932
NM_001457.4(FLNB):c.6928A>G (p.Ile2310Val)
NM_001457.4(FLNB):c.6956T>C (p.Ile2319Thr) rs116826041
NM_001457.4(FLNB):c.7099G>A (p.Val2367Ile) rs115747856
NM_001457.4(FLNB):c.7164C>T (p.Ser2388=) rs757418085
NM_001457.4(FLNB):c.7198+20C>G rs201580886
NM_001457.4(FLNB):c.7254C>T (p.Ser2418=) rs563382903
NM_001457.4(FLNB):c.7255G>A (p.Val2419Ile) rs202143851
NM_001457.4(FLNB):c.762G>A (p.Pro254=) rs371715057
NM_001457.4(FLNB):c.7641C>T (p.Ile2547=) rs139582437
NM_001457.4(FLNB):c.9A>G (p.Val3=) rs199846967

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