ClinVar Miner

List of variants in gene FLNA reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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Gene type:
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Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_001110556.2(FLNA):c.1029C>T (p.Ser343=) rs199853721 0.00118
NM_001110556.2(FLNA):c.1239G>A (p.Thr413=) rs200278701 0.00098
NM_001110556.2(FLNA):c.1579C>T (p.Arg527Cys) rs202029322 0.00046
NM_001110556.2(FLNA):c.3717C>T (p.Pro1239=) rs372265042 0.00046
NM_001110556.2(FLNA):c.1691+7C>A rs199565118 0.00031
NM_001110556.2(FLNA):c.2023-8C>T rs587780335 0.00029
NM_001110556.2(FLNA):c.2178C>T (p.Asn726=) rs371501734 0.00028
NM_001110556.2(FLNA):c.237G>C (p.Ala79=) rs200626788 0.00023
NM_001110556.2(FLNA):c.2813C>T (p.Thr938Met) rs782180774 0.00014
NM_001110556.2(FLNA):c.3045G>A (p.Ala1015=) rs370868704 0.00014
NM_001110556.2(FLNA):c.2725G>A (p.Val909Ile) rs199911951 0.00013
NM_001110556.2(FLNA):c.1238C>T (p.Thr413Met) rs782549299 0.00011
NM_001110556.2(FLNA):c.6307A>G (p.Arg2103Gly) rs370277156 0.00010
NM_001110556.2(FLNA):c.2123G>A (p.Arg708Gln) rs371707134 0.00009
NM_001110556.2(FLNA):c.901C>T (p.Arg301Trp) rs192609440 0.00007
NM_001110556.2(FLNA):c.5710G>A (p.Gly1904Ser) rs782549964 0.00006
NM_001110556.2(FLNA):c.66C>T (p.Asp22=) rs782358007 0.00006
NM_001110556.2(FLNA):c.6394G>A (p.Val2132Met) rs201396725 0.00005
NM_001110556.2(FLNA):c.1964G>A (p.Arg655His) rs782563602 0.00004
NM_001110556.2(FLNA):c.4232C>T (p.Ser1411Leu) rs782426283 0.00004
NM_001110556.2(FLNA):c.1291G>C (p.Glu431Gln) rs781915319 0.00003
NM_001110556.2(FLNA):c.2538C>T (p.Tyr846=) rs782571710 0.00003
NM_001110556.2(FLNA):c.2613C>T (p.Asp871=) rs188212919 0.00003
NM_001110556.2(FLNA):c.4517C>T (p.Thr1506Ile) rs797045579 0.00003
NM_001110556.2(FLNA):c.6846G>A (p.Glu2282=) rs781972193 0.00003
NM_001110556.2(FLNA):c.6863G>A (p.Arg2288His) rs782275601 0.00003
NM_001110556.2(FLNA):c.1000G>A (p.Ala334Thr) rs886044859 0.00002
NM_001110556.2(FLNA):c.1580G>A (p.Arg527His) rs782450368 0.00002
NM_001110556.2(FLNA):c.461T>C (p.Met154Thr) rs782240483 0.00002
NM_001110556.2(FLNA):c.4899C>T (p.Arg1633=) rs781846478 0.00002
NM_001110556.2(FLNA):c.5451G>A (p.Gln1817=) rs782390251 0.00002
NM_001110556.2(FLNA):c.7389G>A (p.Ser2463=) rs373103712 0.00002
NM_001110556.2(FLNA):c.841C>G (p.Pro281Ala) rs2067770833 0.00002
NM_001110556.2(FLNA):c.1372G>A (p.Val458Ile) rs782791907 0.00001
NM_001110556.2(FLNA):c.1765G>A (p.Gly589Ser) rs782371876 0.00001
NM_001110556.2(FLNA):c.2671A>G (p.Lys891Glu) rs1459255199 0.00001
NM_001110556.2(FLNA):c.4222G>A (p.Gly1408Ser) rs797045578 0.00001
NM_001110556.2(FLNA):c.6719A>G (p.Lys2240Arg) rs797045581 0.00001
NM_001110556.2(FLNA):c.6725G>A (p.Arg2242Gln) rs781984274 0.00001
NM_001110556.2(FLNA):c.7051G>A (p.Ala2351Thr) rs1557175653 0.00001
NM_001110556.2(FLNA):c.25G>T (p.Gly9Cys) rs782292045
NM_001110556.2(FLNA):c.4818G>A (p.Val1606=) rs2148109762
NM_001110556.2(FLNA):c.5873T>G (p.Met1958Arg) rs587780336
NM_001110556.2(FLNA):c.6263G>A (p.Ser2088Asn) rs797045580
NM_001110556.2(FLNA):c.6875C>T (p.Ser2292Phe) rs1557175878

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