ClinVar Miner

List of variants in gene combination LOC107982234, WT1 reported by GeneDx

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Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_024426.4(WT1):c.-247T>C rs2234580 0.51534
NM_024426.6(WT1):c.213G>T (p.Pro71=) rs2234582 0.31689
NM_024426.6(WT1):c.662-1785T>G rs11031778 0.19078
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.662-2310C>T rs3847590 0.01761
NM_024426.6(WT1):c.661+161G>T rs5030139 0.01255
NM_024426.6(WT1):c.661+58C>T rs5030138 0.00604
NM_024426.6(WT1):c.662-2299A>C rs192410368 0.00601
NM_024426.6(WT1):c.181C>A (p.Arg61=) rs2234581 0.00270
NM_024426.6(WT1):c.309C>A (p.Gly103=) rs547333427 0.00197
NM_024426.6(WT1):c.123G>C (p.Pro41=) rs555140661 0.00188
NM_024426.6(WT1):c.662-1873_662-1868dup rs1554945689 0.00091
NM_024426.6(WT1):c.216G>T (p.Gln72His) rs5030135 0.00036
NM_024426.6(WT1):c.124G>A (p.Gly42Ser) rs762288656 0.00019
NM_024426.6(WT1):c.193G>A (p.Gly65Arg) rs374404615 0.00019
NM_024426.6(WT1):c.343C>T (p.Pro115Ser) rs916583720 0.00011
NM_024426.6(WT1):c.381C>G (p.Pro127=) rs771681406 0.00009
NM_024426.6(WT1):c.421C>T (p.Pro141Ser) rs750548251 0.00009
NM_024426.6(WT1):c.121C>T (p.Pro41Ser) rs926668379 0.00006
NM_024426.6(WT1):c.513C>A (p.Gly171=) rs536728682 0.00004
NM_024426.6(WT1):c.70C>T (p.Arg24Cys) rs878855086 0.00004
NM_024426.6(WT1):c.151del (p.Ala51fs) rs776155094 0.00003
NM_024426.6(WT1):c.397C>A (p.Pro133Thr) rs1202603651 0.00003
NM_024426.6(WT1):c.475G>A (p.Glu159Lys) rs768165877 0.00003
NM_024426.6(WT1):c.218A>T (p.Gln73Leu) rs1036899554 0.00002
NM_024426.6(WT1):c.586G>A (p.Gly196Ser) rs756501972 0.00002
NM_024426.6(WT1):c.587G>A (p.Gly196Asp) rs753112302 0.00002
NM_024426.6(WT1):c.109G>A (p.Gly37Arg) rs1397886023 0.00001
NM_024426.6(WT1):c.133T>C (p.Trp45Arg) rs1186470250 0.00001
NM_024426.6(WT1):c.284G>T (p.Gly95Val) rs1454795891 0.00001
NM_024426.6(WT1):c.646G>A (p.Ala216Thr) rs778069787 0.00001
NM_024426.6(WT1):c.658C>A (p.Gln220Lys) rs373935628 0.00001
NM_024426.6(WT1):c.77G>A (p.Gly26Glu) rs1484558172 0.00001
NM_024426.6(WT1):c.114C>G (p.Val38=)
NM_024426.6(WT1):c.16_17delinsGG (p.Leu6Gly)
NM_024426.6(WT1):c.203G>A (p.Gly68Glu) rs1170323988
NM_024426.6(WT1):c.28_29delinsTA (p.Ala10Tyr) rs1554946803
NM_024426.6(WT1):c.305G>C (p.Ser102Thr)
NM_024426.6(WT1):c.358G>A (p.Ala120Thr) rs1590410151
NM_024426.6(WT1):c.384G>A (p.Ala128=)
NM_024426.6(WT1):c.405_416dup (p.Pro138_Pro141dup) rs1469499452
NM_024426.6(WT1):c.411GCC[5] (p.Pro141dup) rs760304811
NM_024426.6(WT1):c.500T>C (p.Val167Ala)
NM_024426.6(WT1):c.543_556del (p.Tyr182fs) rs1554946460
NM_024426.6(WT1):c.566C>G (p.Pro189Arg) rs745879965
NM_024426.6(WT1):c.636G>C (p.Glu212Asp)
NM_024426.6(WT1):c.661G>T (p.Gly221Cys)
NM_024426.6(WT1):c.662-1755A>C rs66798575
NM_024426.6(WT1):c.662-1756C>G rs72893517
NM_024426.6(WT1):c.662-1829_662-1828insCC rs1443702205
NM_024426.6(WT1):c.662-1831CT[8] rs370524588
NM_024426.6(WT1):c.662-1836_662-1835dup rs367920789
NM_024426.6(WT1):c.662-2076del rs76500597
NM_024426.6(WT1):c.662-2173G>A rs75870920
NM_024426.6(WT1):c.662-2359C>G rs12575247
NR_023920.2(WT1-AS):n.323C>A rs2234579

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