ClinVar Miner

List of variants in gene SLC26A4 reported as likely benign by Invitae

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Total variants: 184
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HGVS dbSNP
NC_000007.14:g.107660799A>G rs545973091
NM_000441.2(SLC26A4):c.1003T>C (p.Phe335Leu) rs111033212
NM_000441.2(SLC26A4):c.1029G>A (p.Val343=) rs1224284451
NM_000441.2(SLC26A4):c.1040C>T (p.Ser347Leu) rs150946659
NM_000441.2(SLC26A4):c.1050G>A (p.Leu350=) rs727504993
NM_000441.2(SLC26A4):c.1068C>T (p.Ile356=) rs886061885
NM_000441.2(SLC26A4):c.1069G>A (p.Ala357Thr) rs145467740
NM_000441.2(SLC26A4):c.1101A>G (p.Val367=) rs774874269
NM_000441.2(SLC26A4):c.111G>A (p.Glu37=)
NM_000441.2(SLC26A4):c.1137C>T (p.Ile379=)
NM_000441.2(SLC26A4):c.1143G>A (p.Gly381=)
NM_000441.2(SLC26A4):c.1149+9G>T
NM_000441.2(SLC26A4):c.1150-9C>T
NM_000441.2(SLC26A4):c.1152A>G (p.Glu384=)
NM_000441.2(SLC26A4):c.117C>T (p.Arg39=)
NM_000441.2(SLC26A4):c.1194C>T (p.Phe398=) rs1584325099
NM_000441.2(SLC26A4):c.1212C>A (p.Thr404=)
NM_000441.2(SLC26A4):c.1215T>C (p.Thr405=)
NM_000441.2(SLC26A4):c.1224C>T (p.Ser408=)
NM_000441.2(SLC26A4):c.1233C>G (p.Ala411=)
NM_000441.2(SLC26A4):c.1233C>T (p.Ala411=) rs766572560
NM_000441.2(SLC26A4):c.1257G>A (p.Lys419=) rs747564818
NM_000441.2(SLC26A4):c.1264-4C>T rs1488973035
NM_000441.2(SLC26A4):c.1287G>A (p.Ala429=)
NM_000441.2(SLC26A4):c.1299C>T (p.Ile433=) rs397516415
NM_000441.2(SLC26A4):c.1305T>C (p.Ile435=) rs1299422209
NM_000441.2(SLC26A4):c.1312C>T (p.Leu438=)
NM_000441.2(SLC26A4):c.1342-6T>C
NM_000441.2(SLC26A4):c.1348T>C (p.Leu450=)
NM_000441.2(SLC26A4):c.1350G>A (p.Leu450=)
NM_000441.2(SLC26A4):c.135G>T (p.Thr45=) rs756029600
NM_000441.2(SLC26A4):c.1368C>A (p.Ala456=)
NM_000441.2(SLC26A4):c.1368C>T (p.Ala456=)
NM_000441.2(SLC26A4):c.1371C>T (p.Asn457=)
NM_000441.2(SLC26A4):c.1380G>A (p.Gly460=)
NM_000441.2(SLC26A4):c.1428G>A (p.Lys476=)
NM_000441.2(SLC26A4):c.1431T>C (p.Ile477=) rs1584330196
NM_000441.2(SLC26A4):c.1437+7C>A
NM_000441.2(SLC26A4):c.1455G>A (p.Thr485=)
NM_000441.2(SLC26A4):c.1464G>A (p.Val488=)
NM_000441.2(SLC26A4):c.1468A>C (p.Ile490Leu) rs200511789
NM_000441.2(SLC26A4):c.147C>G (p.Ser49Arg) rs756969021
NM_000441.2(SLC26A4):c.147C>T (p.Ser49=)
NM_000441.2(SLC26A4):c.1491T>C (p.Gly497=) rs150860491
NM_000441.2(SLC26A4):c.150G>C (p.Leu50=)
NM_000441.2(SLC26A4):c.1524T>C (p.Thr508=)
NM_000441.2(SLC26A4):c.1544+10G>A
NM_000441.2(SLC26A4):c.1545-5T>C
NM_000441.2(SLC26A4):c.1545-6T>C
NM_000441.2(SLC26A4):c.1545-7del rs727503427
NM_000441.2(SLC26A4):c.1545-8T>C
NM_000441.2(SLC26A4):c.1584T>C (p.Asp528=)
NM_000441.2(SLC26A4):c.1590C>T (p.Tyr530=)
NM_000441.2(SLC26A4):c.1599C>T (p.Thr533=)
NM_000441.2(SLC26A4):c.1608C>T (p.Tyr536=) rs181882513
NM_000441.2(SLC26A4):c.1614+8C>T rs370184422
NM_000441.2(SLC26A4):c.1614+9C>T
NM_000441.2(SLC26A4):c.1614C>T (p.Asn538=) rs111033193
NM_000441.2(SLC26A4):c.1615-4C>A
NM_000441.2(SLC26A4):c.1615-6T>C
NM_000441.2(SLC26A4):c.1615-8A>T
NM_000441.2(SLC26A4):c.1616T>C (p.Ile539Thr) rs146269871
NM_000441.2(SLC26A4):c.1635G>A (p.Val545=)
NM_000441.2(SLC26A4):c.1647A>G (p.Arg549=)
NM_000441.2(SLC26A4):c.1668T>C (p.Tyr556=)
NM_000441.2(SLC26A4):c.1677C>T (p.Val559=)
NM_000441.2(SLC26A4):c.1680T>C (p.Asp560=)
NM_000441.2(SLC26A4):c.1708-4A>G
NM_000441.2(SLC26A4):c.1708-6C>T
NM_000441.2(SLC26A4):c.1744C>T (p.Leu582=)
NM_000441.2(SLC26A4):c.1752G>A (p.Ala584=) rs771015634
NM_000441.2(SLC26A4):c.1752G>T (p.Ala584=)
NM_000441.2(SLC26A4):c.1785A>G (p.Gly595=)
NM_000441.2(SLC26A4):c.1796C>T (p.Ala599Val) rs201709908
NM_000441.2(SLC26A4):c.1803+10C>T
NM_000441.2(SLC26A4):c.1804-7C>T rs1298895017
NM_000441.2(SLC26A4):c.1804-9T>C rs746917249
NM_000441.2(SLC26A4):c.1821T>C (p.Asp607=)
NM_000441.2(SLC26A4):c.1827T>G (p.Val609=)
NM_000441.2(SLC26A4):c.183C>T (p.Ala61=) rs778574810
NM_000441.2(SLC26A4):c.1842T>C (p.Ala614=)
NM_000441.2(SLC26A4):c.1860T>C (p.Asp620=)
NM_000441.2(SLC26A4):c.1887C>A (p.Ile629=)
NM_000441.2(SLC26A4):c.1905G>A (p.Glu635=) rs541538556
NM_000441.2(SLC26A4):c.1923C>T (p.Asn641=)
NM_000441.2(SLC26A4):c.1924T>C (p.Ser642Pro) rs397516423
NM_000441.2(SLC26A4):c.1947C>T (p.Asn649=) rs761139326
NM_000441.2(SLC26A4):c.1965C>T (p.Ile655=)
NM_000441.2(SLC26A4):c.1971C>T (p.Ser657=)
NM_000441.2(SLC26A4):c.1995A>C (p.Ile665=) rs185493402
NM_000441.2(SLC26A4):c.2007C>T (p.Asp669=) rs749013429
NM_000441.2(SLC26A4):c.201T>G (p.Thr67=)
NM_000441.2(SLC26A4):c.2035-7T>C
NM_000441.2(SLC26A4):c.2040C>T (p.Val680=) rs909072667
NM_000441.2(SLC26A4):c.2067T>C (p.Asn689=)
NM_000441.2(SLC26A4):c.2070G>A (p.Val690=) rs374686650
NM_000441.2(SLC26A4):c.2079A>G (p.Ala693=) rs767770720
NM_000441.2(SLC26A4):c.2089+9A>C rs369504960
NM_000441.2(SLC26A4):c.2089+9A>G rs369504960
NM_000441.2(SLC26A4):c.2094T>C (p.Tyr698=)
NM_000441.2(SLC26A4):c.2151A>C (p.Thr717=)
NM_000441.2(SLC26A4):c.2163G>C (p.Thr721=) rs375151702
NM_000441.2(SLC26A4):c.2185C>T (p.Leu729=) rs758851434
NM_000441.2(SLC26A4):c.2190G>T (p.Gln730His) rs142723249
NM_000441.2(SLC26A4):c.21G>A (p.Arg7=)
NM_000441.2(SLC26A4):c.2205T>G (p.Ser735=) rs1387758666
NM_000441.2(SLC26A4):c.2211G>C (p.Glu737Asp) rs200664061
NM_000441.2(SLC26A4):c.2220T>A (p.Gly740=)
NM_000441.2(SLC26A4):c.2223C>T (p.Ser741=)
NM_000441.2(SLC26A4):c.2229A>G (p.Leu743=)
NM_000441.2(SLC26A4):c.2236-6T>C
NM_000441.2(SLC26A4):c.225C>G (p.Leu75=) rs187447337
NM_000441.2(SLC26A4):c.2265C>G (p.Thr755=) rs752928913
NM_000441.2(SLC26A4):c.2283A>G (p.Thr761=) rs202033028
NM_000441.2(SLC26A4):c.2291C>T (p.Thr764Met) rs150597240
NM_000441.2(SLC26A4):c.2292G>A (p.Thr764=) rs139556627
NM_000441.2(SLC26A4):c.2298A>G (p.Glu766=) rs771772382
NM_000441.2(SLC26A4):c.2310C>A (p.Val770=)
NM_000441.2(SLC26A4):c.2310C>T (p.Val770=)
NM_000441.2(SLC26A4):c.2320-4A>G rs727503432
NM_000441.2(SLC26A4):c.2326C>T (p.Arg776Cys) rs111033255
NM_000441.2(SLC26A4):c.258T>C (p.Ser86=)
NM_000441.2(SLC26A4):c.261C>T (p.Asp87=)
NM_000441.2(SLC26A4):c.273A>G (p.Gly91=) rs1365152873
NM_000441.2(SLC26A4):c.288A>C (p.Leu96=)
NM_000441.2(SLC26A4):c.297G>A (p.Thr99=) rs397516429
NM_000441.2(SLC26A4):c.297G>T (p.Thr99=)
NM_000441.2(SLC26A4):c.304+10T>C
NM_000441.2(SLC26A4):c.304+7T>A
NM_000441.2(SLC26A4):c.306G>A (p.Gly102=) rs1584304133
NM_000441.2(SLC26A4):c.312A>C (p.Ala104=)
NM_000441.2(SLC26A4):c.322C>T (p.Leu108=) rs374545905
NM_000441.2(SLC26A4):c.339C>T (p.Val113=) rs780236833
NM_000441.2(SLC26A4):c.33G>T (p.Pro11=)
NM_000441.2(SLC26A4):c.357T>C (p.Ser119=)
NM_000441.2(SLC26A4):c.39C>A (p.Leu13=) rs1562817215
NM_000441.2(SLC26A4):c.402A>G (p.Arg134=)
NM_000441.2(SLC26A4):c.415+10_415+15del
NM_000441.2(SLC26A4):c.426A>T (p.Pro142=) rs555657762
NM_000441.2(SLC26A4):c.441G>A (p.Met147Ile) rs201905280
NM_000441.2(SLC26A4):c.471C>G (p.Pro157=)
NM_000441.2(SLC26A4):c.471C>T (p.Pro157=)
NM_000441.2(SLC26A4):c.474C>T (p.Asp158=)
NM_000441.2(SLC26A4):c.486C>G (p.Leu162=)
NM_000441.2(SLC26A4):c.486C>T (p.Leu162=) rs370020280
NM_000441.2(SLC26A4):c.489A>G (p.Val163=)
NM_000441.2(SLC26A4):c.510A>G (p.Val170=)
NM_000441.2(SLC26A4):c.531C>T (p.Asp177=) rs1584306710
NM_000441.2(SLC26A4):c.535G>A (p.Ala179Thr) rs114473792
NM_000441.2(SLC26A4):c.594T>A (p.Ile198=)
NM_000441.2(SLC26A4):c.594T>C (p.Ile198=)
NM_000441.2(SLC26A4):c.601-4G>A
NM_000441.2(SLC26A4):c.601-5C>T rs546450643
NM_000441.2(SLC26A4):c.627A>G (p.Gly209=)
NM_000441.2(SLC26A4):c.636G>T (p.Val212=)
NM_000441.2(SLC26A4):c.657G>A (p.Leu219=)
NM_000441.2(SLC26A4):c.66G>T (p.Val22=)
NM_000441.2(SLC26A4):c.678T>C (p.Ala226=)
NM_000441.2(SLC26A4):c.684C>G (p.Ala228=)
NM_000441.2(SLC26A4):c.702A>T (p.Ser234=)
NM_000441.2(SLC26A4):c.708A>G (p.Leu236=) rs748961362
NM_000441.2(SLC26A4):c.714T>A (p.Ile238=)
NM_000441.2(SLC26A4):c.747A>C (p.Gly249=)
NM_000441.2(SLC26A4):c.753C>T (p.Leu251=)
NM_000441.2(SLC26A4):c.756T>C (p.Ser252=)
NM_000441.2(SLC26A4):c.75G>C (p.Pro25=) rs570668954
NM_000441.2(SLC26A4):c.75G>T (p.Pro25=)
NM_000441.2(SLC26A4):c.765+7del
NM_000441.2(SLC26A4):c.768G>A (p.Thr256=)
NM_000441.2(SLC26A4):c.801C>A (p.Thr267=)
NM_000441.2(SLC26A4):c.819T>C (p.Thr273=) rs1160800485
NM_000441.2(SLC26A4):c.840C>T (p.Val280=) rs759467038
NM_000441.2(SLC26A4):c.843C>G (p.Val281=) rs1584317556
NM_000441.2(SLC26A4):c.870T>C (p.Asp290=)
NM_000441.2(SLC26A4):c.873G>A (p.Arg291=) rs776517641
NM_000441.2(SLC26A4):c.879A>G (p.Arg293=)
NM_000441.2(SLC26A4):c.903T>C (p.Pro301=)
NM_000441.2(SLC26A4):c.90C>G (p.Leu30=) rs566715839
NM_000441.2(SLC26A4):c.948A>C (p.Gly316=) rs876657583
NM_000441.2(SLC26A4):c.957G>A (p.Leu319=)
NM_000441.2(SLC26A4):c.964A>G (p.Asn322Asp) rs143002265
NM_000441.2(SLC26A4):c.969C>T (p.Tyr323=)
NM_000441.2(SLC26A4):c.987A>G (p.Lys329=)
NM_000441.2(SLC26A4):c.990C>T (p.Ser330=)

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