ClinVar Miner

List of variants in gene FLNA reported as uncertain significance by Eurofins NTD LLC (GA)

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Gene type:
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Total variants: 77
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HGVS dbSNP gnomAD frequency
NM_001110556.2(FLNA):c.1875C>T (p.Asp625=) rs200660642 0.00140
NM_001110556.2(FLNA):c.1191C>T (p.Ile397=) rs200048692 0.00071
NM_001110556.2(FLNA):c.1450C>T (p.Arg484Trp) rs61730768 0.00047
NM_001110556.2(FLNA):c.4179G>A (p.Glu1393=) rs182074603 0.00033
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.6412G>T (p.Gly2138Cys) rs200524526 0.00023
NM_001110556.2(FLNA):c.3285C>T (p.Ala1095=) rs199530601 0.00019
NM_001110556.2(FLNA):c.1812C>T (p.Asp604=) rs370735674 0.00015
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.1933G>A (p.Val645Ile) rs373286506 0.00012
NM_001110556.2(FLNA):c.5715G>A (p.Pro1905=) rs367674709 0.00012
NM_001110556.2(FLNA):c.6993C>T (p.Asp2331=) rs201153928 0.00011
NM_001110556.2(FLNA):c.3708C>T (p.Gly1236=) rs200363918 0.00010
NM_001110556.2(FLNA):c.4857C>T (p.Leu1619=) rs368536975 0.00010
NM_001110556.2(FLNA):c.6227-7C>T rs370491691 0.00010
NM_001110556.2(FLNA):c.6804T>C (p.Ala2268=) rs376461465 0.00010
NM_001110556.2(FLNA):c.7362G>A (p.Thr2454=) rs369179210 0.00010
NM_001110556.2(FLNA):c.3379G>A (p.Val1127Met) rs398123617 0.00007
NM_001110556.2(FLNA):c.7172G>A (p.Arg2391His) rs727503930 0.00007
NM_001110556.2(FLNA):c.901C>T (p.Arg301Trp) rs192609440 0.00007
NM_001110556.2(FLNA):c.5448G>A (p.Ala1816=) rs782806731 0.00006
NM_001110556.2(FLNA):c.3555C>T (p.Cys1185=) rs1477689141 0.00005
NM_001110556.2(FLNA):c.4237G>A (p.Glu1413Lys) rs886044833 0.00005
NM_001110556.2(FLNA):c.4263C>T (p.Thr1421=) rs398123618 0.00005
NM_001110556.2(FLNA):c.6770-5C>T rs370913359 0.00005
NM_001110556.2(FLNA):c.7052C>G (p.Ala2351Gly) rs782583650 0.00005
NM_001110556.2(FLNA):c.1964G>A (p.Arg655His) rs782563602 0.00004
NM_001110556.2(FLNA):c.3216G>A (p.Ala1072=) rs782006734 0.00004
NM_001110556.2(FLNA):c.3330G>A (p.Ala1110=) rs781917512 0.00004
NM_001110556.2(FLNA):c.5218-4G>A rs370196495 0.00004
NM_001110556.2(FLNA):c.6175G>A (p.Glu2059Lys) rs782779958 0.00004
NM_001110556.2(FLNA):c.1110C>T (p.Phe370=) rs886044869 0.00003
NM_001110556.2(FLNA):c.1242C>T (p.Gly414=) rs782598234 0.00003
NM_001110556.2(FLNA):c.3367T>G (p.Ser1123Ala) rs368441729 0.00003
NM_001110556.2(FLNA):c.4106C>T (p.Thr1369Ile) rs376774130 0.00003
NM_001110556.2(FLNA):c.6108G>A (p.Pro2036=) rs782221205 0.00003
NM_001110556.2(FLNA):c.627G>A (p.Leu209=) rs782118838 0.00003
NM_001110556.2(FLNA):c.6871G>A (p.Gly2291Ser) rs797044739 0.00003
NM_001110556.2(FLNA):c.6997C>T (p.Arg2333Cys) rs781984348 0.00003
NM_001110556.2(FLNA):c.1000G>A (p.Ala334Thr) rs886044859 0.00002
NM_001110556.2(FLNA):c.2162C>T (p.Ala721Val) rs781840723 0.00002
NM_001110556.2(FLNA):c.623-7G>A rs782670288 0.00002
NM_001110556.2(FLNA):c.7259T>C (p.Val2420Ala) rs782289803 0.00002
NM_001110556.2(FLNA):c.1287G>A (p.Thr429=) rs782263267 0.00001
NM_001110556.2(FLNA):c.2281-6C>T rs1248116977 0.00001
NM_001110556.2(FLNA):c.2472C>T (p.Phe824=) rs782669943 0.00001
NM_001110556.2(FLNA):c.2550C>T (p.Val850=) rs782623139 0.00001
NM_001110556.2(FLNA):c.3147C>T (p.Gly1049=) rs398123615 0.00001
NM_001110556.2(FLNA):c.3323G>A (p.Cys1108Tyr) rs371677498 0.00001
NM_001110556.2(FLNA):c.4474+3G>T rs1286863443 0.00001
NM_001110556.2(FLNA):c.5714C>T (p.Pro1905Leu) rs781794030 0.00001
NM_001110556.2(FLNA):c.6047C>T (p.Thr2016Met) rs781946802 0.00001
NM_001110556.2(FLNA):c.7013C>G (p.Ser2338Cys) rs781878646 0.00001
NM_001110556.2(FLNA):c.7245C>T (p.Pro2415=) rs886044822 0.00001
NM_001110556.2(FLNA):c.902G>T (p.Arg301Leu) rs371600068 0.00001
NM_001110556.2(FLNA):c.1107C>T (p.Pro369=) rs886044791
NM_001110556.2(FLNA):c.134A>G (p.Gln45Arg) rs398123613
NM_001110556.2(FLNA):c.2826+7A>G rs782545599
NM_001110556.2(FLNA):c.2952C>G (p.Asp984Glu) rs782513930
NM_001110556.2(FLNA):c.3054C>G (p.Cys1018Trp) rs886044871
NM_001110556.2(FLNA):c.3282C>G (p.Gly1094=) rs369583365
NM_001110556.2(FLNA):c.3348C>A (p.Asp1116Glu) rs797044684
NM_001110556.2(FLNA):c.3896A>G (p.Asn1299Ser) rs1569551645
NM_001110556.2(FLNA):c.3930G>A (p.Gln1310=) rs1557177599
NM_001110556.2(FLNA):c.586C>T (p.Arg196Trp) rs137853317
NM_001110556.2(FLNA):c.5938C>T (p.Leu1980Phe) rs886044866
NM_001110556.2(FLNA):c.623-3C>G rs398123622
NM_001110556.2(FLNA):c.6291G>A (p.Leu2097=) rs782667495
NM_001110556.2(FLNA):c.6691G>A (p.Gly2231Arg) rs797044738
NM_001110556.2(FLNA):c.687G>T (p.Met229Ile) rs886044820
NM_001110556.2(FLNA):c.7092C>A (p.Ile2364=) rs782591917
NM_001110556.2(FLNA):c.7103T>C (p.Val2368Ala) rs1557175620
NM_001110556.2(FLNA):c.733G>A (p.Glu245Lys) rs797044753

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