ClinVar Miner

List of variants in gene SLC26A4 reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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Total variants: 29
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HGVS dbSNP gnomAD frequency
NM_000441.2(SLC26A4):c.2326C>T (p.Arg776Cys) rs111033255 0.00183
NM_000441.2(SLC26A4):c.964A>G (p.Asn322Asp) rs143002265 0.00139
NM_000441.2(SLC26A4):c.1061T>C (p.Phe354Ser) rs111033243 0.00083
NM_000441.2(SLC26A4):c.1614C>T (p.Asn538=) rs111033193 0.00069
NM_000441.2(SLC26A4):c.1947C>T (p.Asn649=) rs761139326 0.00017
NM_000441.2(SLC26A4):c.90C>G (p.Leu30=) rs566715839 0.00013
NM_000441.2(SLC26A4):c.796G>A (p.Asp266Asn) rs138462416 0.00010
NM_000441.2(SLC26A4):c.61A>G (p.Met21Val) rs375716219 0.00009
NM_000441.2(SLC26A4):c.841G>A (p.Val281Ile) rs727505080 0.00009
NM_000441.2(SLC26A4):c.1468A>C (p.Ile490Leu) rs200511789 0.00006
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.322C>T (p.Leu108=) rs374545905 0.00004
NM_000441.2(SLC26A4):c.1740G>A (p.Lys580=) rs573894071 0.00003
NM_000441.2(SLC26A4):c.2007C>T (p.Asp669=) rs749013429 0.00002
NM_000441.2(SLC26A4):c.200C>G (p.Thr67Ser) rs111033240 0.00002
NM_000441.2(SLC26A4):c.1050G>A (p.Leu350=) rs727504993 0.00001
NM_000441.2(SLC26A4):c.1299C>T (p.Ile433=) rs397516415 0.00001
NM_000441.2(SLC26A4):c.1342-10C>T rs727503426 0.00001
NM_000441.2(SLC26A4):c.1608C>T (p.Tyr536=) rs181882513 0.00001
NM_000441.2(SLC26A4):c.1871T>C (p.Leu624Pro) rs1345776426 0.00001
NM_000441.2(SLC26A4):c.2320-4A>C rs727503432 0.00001
NM_000441.2(SLC26A4):c.297G>A (p.Thr99=) rs397516429 0.00001
NM_000441.2(SLC26A4):c.948A>C (p.Gly316=) rs876657583 0.00001
NM_000441.1(SLC26A4):c.-66C>T rs17154282
NM_000441.2(SLC26A4):c.1545-14_1545-12del rs397516419
NM_000441.2(SLC26A4):c.2029C>A (p.Arg677=) rs397516426
NM_000441.2(SLC26A4):c.486C>T (p.Leu162=) rs370020280
NM_000441.2(SLC26A4):c.75G>C (p.Pro25=) rs570668954

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