ClinVar Miner

List of variants in gene SLC26A4 reported as uncertain significance by EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

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Total variants: 14
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HGVS dbSNP
NM_000441.1(SLC26A4):c.1040C>T (p.Ser347Leu) rs150946659
NM_000441.1(SLC26A4):c.1233C>T (p.Ala411=) rs766572560
NM_000441.1(SLC26A4):c.147C>G (p.Ser49Arg) rs756969021
NM_000441.1(SLC26A4):c.1572C>T (p.Ile524=)
NM_000441.1(SLC26A4):c.1614C>T (p.Asn538=) rs111033193
NM_000441.1(SLC26A4):c.1673A>G (p.Asn558Ser)
NM_000441.1(SLC26A4):c.1730T>C (p.Val577Ala) rs56017519
NM_000441.1(SLC26A4):c.1852G>A (p.Asp618Asn) rs886043208
NM_000441.1(SLC26A4):c.1905G>A (p.Glu635=) rs541538556
NM_000441.1(SLC26A4):c.2227T>G (p.Leu743Val) rs780626619
NM_000441.1(SLC26A4):c.2283A>G (p.Thr761=) rs202033028
NM_000441.1(SLC26A4):c.236G>A (p.Arg79Gln) rs200706874
NM_000441.1(SLC26A4):c.28C>A (p.Pro10Thr) rs200102493
NM_000441.1(SLC26A4):c.845G>A (p.Cys282Tyr) rs111033454

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