ClinVar Miner

List of variants in gene SLC26A4 studied for Hearing impairment

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Total variants: 13
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HGVS dbSNP
NM_000441.2(SLC26A4):c.-103T>C rs60284988
NM_000441.2(SLC26A4):c.1146C>G (p.Asn382Lys)
NM_000441.2(SLC26A4):c.1489G>A (p.Gly497Ser) rs111033308
NM_000441.2(SLC26A4):c.1693T>G (p.Cys565Gly) rs767255075
NM_000441.2(SLC26A4):c.1730T>C (p.Val577Ala) rs56017519
NM_000441.2(SLC26A4):c.2211G>C (p.Glu737Asp) rs200664061
NM_000441.2(SLC26A4):c.2219G>T (p.Gly740Val) rs111033310
NM_000441.2(SLC26A4):c.225C>G (p.Leu75=) rs187447337
NM_000441.2(SLC26A4):c.299T>C (p.Leu100Pro) rs1057518810
NM_000441.2(SLC26A4):c.412G>T (p.Val138Phe) rs111033199
NM_000441.2(SLC26A4):c.445G>A (p.Gly149Arg) rs761210511
NM_000441.2(SLC26A4):c.530A>C (p.Asp177Ala)
NM_000441.2(SLC26A4):c.707T>C (p.Leu236Pro) rs80338848

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