ClinVar Miner

List of variants in gene SLC26A4 reported as benign

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Gene type:
ClinVar version:
Total variants: 80
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HGVS dbSNP gnomAD frequency
NM_000441.2(SLC26A4):c.304+316C>T rs2701686 0.75222
NM_000441.2(SLC26A4):c.165-119A>T rs2248464 0.75124
NM_000441.2(SLC26A4):c.601-266T>G rs3817613 0.73053
NM_000441.2(SLC26A4):c.165-113C>T rs2248465 0.70026
NM_000441.2(SLC26A4):c.1264-187C>T rs2072065 0.45793
NM_000441.2(SLC26A4):c.2035-210C>T rs6955309 0.45116
NM_000441.2(SLC26A4):c.1264-335T>A rs2072064 0.20616
NM_000441.2(SLC26A4):c.*868G>A rs2712218 0.17928
NM_000441.2(SLC26A4):c.765+194A>G rs796938107 0.08403
NM_000441.2(SLC26A4):c.1150-135C>T rs2072063 0.05099
NM_000441.2(SLC26A4):c.-4+90T>G rs73191607 0.04621
NM_000441.2(SLC26A4):c.*1797G>C rs76820337 0.04454
NM_000441.2(SLC26A4):c.1826T>G (p.Val609Gly) rs17154335 0.04399
NM_000441.2(SLC26A4):c.1707+76G>C rs17154331 0.03636
NM_000441.2(SLC26A4):c.1707+211T>C rs76779706 0.03623
NM_000441.2(SLC26A4):c.1263+319T>C rs77056079 0.02613
NM_000441.2(SLC26A4):c.1708-18T>A rs55701254 0.02432
NM_000441.2(SLC26A4):c.2236-151G>T rs78318785 0.02406
NM_000441.2(SLC26A4):c.416-196C>T rs55943182 0.01761
NM_000441.2(SLC26A4):c.164+150T>A rs17154285 0.01613
NM_000441.2(SLC26A4):c.1437+187T>G rs74576945 0.01573
NM_000441.2(SLC26A4):c.1438-258G>T rs116496816 0.01573
NM_000441.2(SLC26A4):c.1001+168A>G rs28566998 0.01549
NM_000441.2(SLC26A4):c.*1302T>G rs112019874 0.01487
NM_000441.2(SLC26A4):c.2218G>A (p.Gly740Ser) rs17154353 0.01449
NM_000441.2(SLC26A4):c.970A>T (p.Asn324Tyr) rs36039758 0.01056
NM_000441.2(SLC26A4):c.1002-9A>C rs10234822 0.01002
NM_000441.2(SLC26A4):c.1438-14A>G rs79531981 0.00882
NM_000441.2(SLC26A4):c.*614C>T rs77315223 0.00874
NM_000441.2(SLC26A4):c.*11G>A rs113496951 0.00867
NM_000441.2(SLC26A4):c.1488C>T (p.Leu496=) rs77407094 0.00782
NM_000441.2(SLC26A4):c.15C>A (p.Gly5=) rs7811324 0.00669
NM_000441.2(SLC26A4):c.1790T>C (p.Leu597Ser) rs55638457 0.00545
NM_000441.2(SLC26A4):c.416-13T>C rs77553387 0.00455
NM_000441.2(SLC26A4):c.898A>C (p.Ile300Leu) rs111033304 0.00450
NM_000441.2(SLC26A4):c.565G>T (p.Ala189Ser) rs35045430 0.00378
NM_000441.2(SLC26A4):c.1341+47T>C rs17154326 0.00317
NM_000441.2(SLC26A4):c.601-17C>T rs78330939 0.00296
NM_000441.2(SLC26A4):c.849G>C (p.Met283Ile) rs146348818 0.00293
NM_000441.2(SLC26A4):c.1545-5T>G rs77944876 0.00234
NM_000441.1(SLC26A4):c.-103T>C rs60284988 0.00209
NM_000441.2(SLC26A4):c.416-7T>C rs111033387 0.00178
NM_000441.2(SLC26A4):c.1069G>A (p.Ala357Thr) rs145467740 0.00166
NM_000441.2(SLC26A4):c.*69C>A rs76894072 0.00061
NM_000441.2(SLC26A4):c.1614+7A>G rs199643344 0.00034
NM_000441.2(SLC26A4):c.1614+8C>T rs370184422 0.00032
NM_000441.2(SLC26A4):c.1001+30A>G rs556184448 0.00026
NM_000441.2(SLC26A4):c.2236-25T>A rs2301634 0.00026
NM_000441.2(SLC26A4):c.1544+9C>T rs368970459 0.00021
NM_000441.2(SLC26A4):c.919-18T>G rs767147359 0.00017
NM_000441.2(SLC26A4):c.1804-6G>A rs377713770 0.00016
NM_000441.2(SLC26A4):c.858G>A (p.Lys286=) rs746111836 0.00013
NM_000441.2(SLC26A4):c.17G>T (p.Gly6Val) rs111033423 0.00010
NM_000441.2(SLC26A4):c.841G>A (p.Val281Ile) rs727505080 0.00009
NM_000441.2(SLC26A4):c.1470C>T (p.Ile490=) rs140918297 0.00006
NM_000441.2(SLC26A4):c.147C>G (p.Ser49Arg) rs756969021 0.00004
NM_000441.2(SLC26A4):c.1363A>T (p.Ile455Phe) rs375576481 0.00003
NM_000441.2(SLC26A4):c.1740G>A (p.Lys580=) rs573894071 0.00003
NM_000441.2(SLC26A4):c.1983C>A (p.Asp661Glu) rs199588131 0.00002
NM_000441.2(SLC26A4):c.-66C>G rs17154282
NM_000441.2(SLC26A4):c.1001+131G>T rs2395911
NM_000441.2(SLC26A4):c.1438-105del rs367623525
NM_000441.2(SLC26A4):c.1438-320C>A rs2188561
NM_000441.2(SLC26A4):c.1438-7del rs753586849
NM_000441.2(SLC26A4):c.1438-7dup rs753586849
NM_000441.2(SLC26A4):c.1545-14_1545-12del rs397516419
NM_000441.2(SLC26A4):c.1615-140del rs35161285
NM_000441.2(SLC26A4):c.1615-141_1615-140del rs35161285
NM_000441.2(SLC26A4):c.1615-142_1615-140del rs35161285
NM_000441.2(SLC26A4):c.199A>C (p.Thr67Pro) rs1174526823
NM_000441.2(SLC26A4):c.2035-9del
NM_000441.2(SLC26A4):c.2235+135dup rs111316118
NM_000441.2(SLC26A4):c.2320-173_2320-172del rs369432913
NM_000441.2(SLC26A4):c.2320-173_2320-172dup rs369432913
NM_000441.2(SLC26A4):c.416-16G>T rs114992866
NM_000441.2(SLC26A4):c.416-7del rs765579453
NM_000441.2(SLC26A4):c.416-8_416-7del
NM_000441.2(SLC26A4):c.765+196_765+197del rs60022317
NM_000441.2(SLC26A4):c.765+197del rs60022317
NM_000441.2(SLC26A4):c.766-20A>C

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