ClinVar Miner

List of variants in gene INSR studied for not specified

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Total variants: 47
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HGVS dbSNP
NM_000208.3(INSR):c.1080C>T (p.Cys360=) rs56066516
NM_000208.3(INSR):c.1084G>A (p.Val362Ile) rs72549237
NM_000208.3(INSR):c.151G>A (p.Glu51Lys) rs140852238
NM_000208.3(INSR):c.190T>C (p.Leu64=) rs144836032
NM_000208.3(INSR):c.2117C>A (p.Ala706Asp) rs142391704
NM_000208.3(INSR):c.2193G>A (p.Thr731=) rs6413501
NM_000208.3(INSR):c.2243C>T (p.Ser748Leu) rs143523271
NM_000208.3(INSR):c.225C>T (p.Asp75=) rs41352749
NM_000208.3(INSR):c.2293G>A (p.Gly765Ser) rs146698985
NM_000208.3(INSR):c.2295C>T (p.Gly765=) rs142654992
NM_000208.3(INSR):c.2355G>A (p.Ser785=) rs148137322
NM_000208.3(INSR):c.2598C>T (p.Val866=) rs797045625
NM_000208.3(INSR):c.2736G>A (p.Arg912=) rs147125937
NM_000208.3(INSR):c.2838C>G (p.Asp946Glu) rs146588336
NM_000208.3(INSR):c.2971C>A (p.Leu991Ile) rs150114699
NM_000208.3(INSR):c.3034G>A (p.Val1012Met) rs1799816
NM_000208.3(INSR):c.3410T>C (p.Ile1137Thr) rs775854644
NM_000208.3(INSR):c.3775G>A (p.Asp1259Asn) rs369102740
NM_000208.3(INSR):c.5C>G (p.Ala2Gly) rs7508518
NM_000208.3(INSR):c.653-5_653-4del rs3835070
NM_000208.3(INSR):c.653-5_653-4dupTC rs3835070
NM_000208.3(INSR):c.653-5_653-4insTC rs1555746859
NM_000208.3(INSR):c.653-7_653-4del rs3835070
NM_000208.3(INSR):c.653-7_653-6insTC rs1555746860
NM_000208.3(INSR):c.653-9_653-7delTCTinsC
NM_000208.3(INSR):c.687C>T (p.Thr229=) rs150568177
NM_000208.3(INSR):c.84C>A (p.His28Gln) rs755298967
NM_000208.3(INSR):c.959C>T (p.Thr320Met) rs138528064
NM_001079817.2(INSR):c.1123+13G>T rs72549236
NM_001079817.2(INSR):c.1483+31T>C rs2860178
NM_001079817.2(INSR):c.1610+23C>T rs9676400
NM_001079817.2(INSR):c.1610+28A>C rs2860177
NM_001079817.2(INSR):c.1638C>T (p.Asp546=) rs2229429
NM_001079817.2(INSR):c.1650G>A (p.Ala550=) rs2059806
NM_001079817.2(INSR):c.1861+27C>T rs3815902
NM_001079817.2(INSR):c.1862-20A>G rs2245648
NM_001079817.2(INSR):c.1862-4A>G rs2245649
NM_001079817.2(INSR):c.2231+20C>A rs6413502
NM_001079817.2(INSR):c.2806+33G>A rs35169098
NM_001079817.2(INSR):c.2807-5T>G rs1555736265
NM_001079817.2(INSR):c.2997C>T (p.Tyr999=) rs1799815
NM_001079817.2(INSR):c.3219C>T (p.His1073=) rs1799817
NM_001079817.2(INSR):c.3223-31C>T rs148813626
NM_001079817.2(INSR):c.3632G>A (p.Gly1211Asp) rs1555734564
NM_001079817.2(INSR):c.421C>T (p.Arg141Trp) rs1555689823
NM_001079817.2(INSR):c.783C>T (p.Asp261=) rs891087
NM_001079817.2(INSR):c.870C>T (p.His290=) rs74483718

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