ClinVar Miner

List of variants in gene SLC26A4 reported as likely benign for not specified

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Gene type:
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Total variants: 46
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HGVS dbSNP
NC_000007.14:g.107674234C>T
NC_000007.14:g.107701133G>A
NC_000007.14:g.107701894T>C
NM_000441.1(SLC26A4):c.-66C>T rs17154282
NM_000441.2(SLC26A4):c.1050G>A (p.Leu350=) rs727504993
NM_000441.2(SLC26A4):c.1061T>C (p.Phe354Ser) rs111033243
NM_000441.2(SLC26A4):c.1069G>A (p.Ala357Thr) rs145467740
NM_000441.2(SLC26A4):c.1299C>T (p.Ile433=) rs397516415
NM_000441.2(SLC26A4):c.1342-10C>T rs727503426
NM_000441.2(SLC26A4):c.1468A>C (p.Ile490Leu) rs200511789
NM_000441.2(SLC26A4):c.1470C>T (p.Ile490=) rs140918297
NM_000441.2(SLC26A4):c.147C>G (p.Ser49Arg) rs756969021
NM_000441.2(SLC26A4):c.1488C>T (p.Leu496=) rs77407094
NM_000441.2(SLC26A4):c.1545-14_1545-12del rs397516419
NM_000441.2(SLC26A4):c.1545-3T>C rs1449532089
NM_000441.2(SLC26A4):c.1545-5T>G rs77944876
NM_000441.2(SLC26A4):c.15C>A (p.Gly5=) rs7811324
NM_000441.2(SLC26A4):c.1608C>T (p.Tyr536=) rs181882513
NM_000441.2(SLC26A4):c.1614+7A>G
NM_000441.2(SLC26A4):c.1614C>T (p.Asn538=) rs111033193
NM_000441.2(SLC26A4):c.17G>T (p.Gly6Val) rs111033423
NM_000441.2(SLC26A4):c.1826T>G (p.Val609Gly) rs17154335
NM_000441.2(SLC26A4):c.183C>T (p.Ala61=) rs778574810
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.2007C>T (p.Asp669=) rs749013429
NM_000441.2(SLC26A4):c.200C>G (p.Thr67Ser) rs111033240
NM_000441.2(SLC26A4):c.2029C>A (p.Arg677=) rs397516426
NM_000441.2(SLC26A4):c.2100A>G (p.Ile700Met) rs1057520633
NM_000441.2(SLC26A4):c.2139T>G (p.Ile713Met) rs143708308
NM_000441.2(SLC26A4):c.2190G>T (p.Gln730His) rs142723249
NM_000441.2(SLC26A4):c.2218G>A (p.Gly740Ser) rs17154353
NM_000441.2(SLC26A4):c.2320-4A>C rs727503432
NM_000441.2(SLC26A4):c.2326C>T (p.Arg776Cys) rs111033255
NM_000441.2(SLC26A4):c.297G>A (p.Thr99=) rs397516429
NM_000441.2(SLC26A4):c.322C>T (p.Leu108=) rs374545905
NM_000441.2(SLC26A4):c.416-7T>C rs111033387
NM_000441.2(SLC26A4):c.565G>T (p.Ala189Ser) rs35045430
NM_000441.2(SLC26A4):c.61A>G (p.Met21Val) rs375716219
NM_000441.2(SLC26A4):c.75G>C (p.Pro25=) rs570668954
NM_000441.2(SLC26A4):c.796G>A (p.Asp266Asn) rs138462416
NM_000441.2(SLC26A4):c.841G>A (p.Val281Ile) rs727505080
NM_000441.2(SLC26A4):c.898A>C (p.Ile300Leu) rs111033304
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.964A>G (p.Asn322Asp) rs143002265

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