ClinVar Miner

List of variants in gene SLC26A4 reported as uncertain significance by Natera, Inc.

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Gene type:
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Total variants: 25
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HGVS dbSNP
NM_000441.1(SLC26A4):c.28C>A (p.Pro10Thr) rs200102493
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.1069G>A (p.Ala357Thr) rs145467740
NM_000441.2(SLC26A4):c.1234G>A (p.Val412Ile) rs111033527
NM_000441.2(SLC26A4):c.1264-4C>T rs1488973035
NM_000441.2(SLC26A4):c.1616T>C (p.Ile539Thr) rs146269871
NM_000441.2(SLC26A4):c.1696A>G (p.Ile566Val)
NM_000441.2(SLC26A4):c.187G>A (p.Gly63Ser)
NM_000441.2(SLC26A4):c.1969A>T (p.Ser657Cys) rs876658003
NM_000441.2(SLC26A4):c.1983C>A (p.Asp661Glu) rs199588131
NM_000441.2(SLC26A4):c.1996T>A (p.Ser666Thr) rs397516425
NM_000441.2(SLC26A4):c.2003T>C (p.Leu668Pro) rs727504303
NM_000441.2(SLC26A4):c.2070G>A (p.Val690=) rs374686650
NM_000441.2(SLC26A4):c.2089+9A>G rs369504960
NM_000441.2(SLC26A4):c.2151A>C (p.Thr717=)
NM_000441.2(SLC26A4):c.2219G>T (p.Gly740Val) rs111033310
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.2326C>T (p.Arg776Cys) rs111033255
NM_000441.2(SLC26A4):c.463A>G (p.Met155Val) rs201931861
NM_000441.2(SLC26A4):c.697G>C (p.Val233Leu) rs397516431
NM_000441.2(SLC26A4):c.871C>T (p.Arg291Trp) rs775610413
NM_000441.2(SLC26A4):c.964A>G (p.Asn322Asp) rs143002265
NM_000441.2(SLC26A4):c.977G>C (p.Gly326Ala)

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