ClinVar Miner

List of variants in gene SALL4 reported as uncertain significance by Eurofins NTD LLC (GA)

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Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_020436.5(SALL4):c.2376T>C (p.Asn792=) rs143601538 0.00146
NM_020436.5(SALL4):c.1287T>G (p.Phe429Leu) rs143818932 0.00106
NM_020436.5(SALL4):c.2041G>A (p.Ala681Thr) rs147385529 0.00056
NM_020436.5(SALL4):c.24A>G (p.Lys8=) rs149430070 0.00039
NM_020436.5(SALL4):c.1630C>T (p.Pro544Ser) rs150402866 0.00031
NM_020436.5(SALL4):c.702G>A (p.Gln234=) rs146143890 0.00028
NM_020436.5(SALL4):c.1358A>G (p.Asn453Ser) rs146644204 0.00026
NM_020436.5(SALL4):c.1104G>A (p.Ala368=) rs142357063 0.00013
NM_020436.5(SALL4):c.1020C>T (p.Gly340=) rs142790611 0.00011
NM_020436.5(SALL4):c.1871C>T (p.Thr624Met) rs146604877 0.00011
NM_020436.5(SALL4):c.2036C>G (p.Thr679Ser) rs549741547 0.00006
NM_020436.5(SALL4):c.216C>T (p.His72=) rs138604469 0.00003
NM_020436.5(SALL4):c.2447G>A (p.Arg816His) rs747560279 0.00003
NM_020436.5(SALL4):c.3153G>A (p.Ala1051=) rs142551587 0.00003
NM_020436.5(SALL4):c.766A>G (p.Thr256Ala) rs139802240 0.00003
NM_020436.5(SALL4):c.1226C>G (p.Pro409Arg) rs1282224804 0.00002
NM_020436.5(SALL4):c.2277G>C (p.Leu759Phe) rs781770955 0.00002
NM_020436.5(SALL4):c.2349A>G (p.Thr783=) rs145820443 0.00002
NM_020436.5(SALL4):c.1005T>C (p.Leu335=) rs150350828 0.00001
NM_020436.5(SALL4):c.1567G>C (p.Gly523Arg) rs113920122 0.00001
NM_020436.5(SALL4):c.2386G>A (p.Glu796Lys) rs886044039 0.00001
NM_020436.5(SALL4):c.2409C>T (p.Pro803=) rs753647133 0.00001
NM_020436.5(SALL4):c.675G>A (p.Gln225=) rs771370612 0.00001
NM_020436.5(SALL4):c.-7T>G rs886042721
NM_020436.5(SALL4):c.2482A>T (p.Thr828Ser) rs764444344
NM_020436.5(SALL4):c.2977G>A (p.Gly993Arg) rs138891224
NM_020436.5(SALL4):c.3161A>G (p.Ter1054=) rs1555848961

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