ClinVar Miner

List of variants in gene combination LOC107982234, WT1 reported by PreventionGenetics, part of Exact Sciences

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Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_024426.6(WT1):c.213G>T (p.Pro71=) rs2234582 0.31689
NM_024426.6(WT1):c.345C>T (p.Pro115=) rs1799925 0.15374
NM_024426.6(WT1):c.609C>T (p.Asn203=) rs2234583 0.13287
NM_024426.6(WT1):c.662-1928_662-1927del rs71873106 0.02282
NM_024426.6(WT1):c.181C>A (p.Arg61=) rs2234581 0.00270
NM_024426.6(WT1):c.123G>C (p.Pro41=) rs555140661 0.00188
NM_024426.6(WT1):c.375C>T (p.Gly125=) rs776209354 0.00039
NM_024426.6(WT1):c.216G>T (p.Gln72His) rs5030135 0.00036
NM_024426.6(WT1):c.-106C>T rs867975105 0.00021
NM_024426.6(WT1):c.381C>G (p.Pro127=) rs771681406 0.00009
NM_024426.6(WT1):c.615C>G (p.Pro205=) rs769467940 0.00005
NM_024426.6(WT1):c.513C>A (p.Gly171=) rs536728682 0.00004
NM_024426.6(WT1):c.151del (p.Ala51fs) rs776155094 0.00003
NM_024426.6(WT1):c.27G>A (p.Pro9=) rs556835183 0.00001
NM_024426.6(WT1):c.286G>A (p.Gly96Ser) rs1060501254 0.00001
NM_024426.6(WT1):c.75C>T (p.Ser25=) rs1417997475 0.00001
NM_024426.6(WT1):c.145G>C (p.Gly49Arg)
NM_024426.6(WT1):c.174C>G (p.Leu58=) rs886048232
NM_024426.6(WT1):c.24C>T (p.Asp8=)
NM_024426.6(WT1):c.261C>A (p.Ala87=)
NM_024426.6(WT1):c.28G>T (p.Ala10Ser) rs1351753257
NM_024426.6(WT1):c.381del (p.Ala128fs)
NM_024426.6(WT1):c.390A>C (p.Pro130=)
NM_024426.6(WT1):c.456C>A (p.Gly152=) rs2133103187
NM_024426.6(WT1):c.543C>T (p.Arg181=) rs369870529
NM_024426.6(WT1):c.619del (p.Leu207fs)
NM_024426.6(WT1):c.99A>G (p.Pro33=) rs2133107306

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