ClinVar Miner

List of variants in gene INSR studied for not specified

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Total variants: 56
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HGVS dbSNP
NM_000208.4(INSR):c.1080C>T (p.Cys360=) rs56066516
NM_000208.4(INSR):c.1084G>A (p.Val362Ile) rs72549237
NM_000208.4(INSR):c.1123+13G>T rs72549236
NM_000208.4(INSR):c.1123+21G>A rs13306458
NM_000208.4(INSR):c.1483+31T>C rs2860178
NM_000208.4(INSR):c.151G>A (p.Glu51Lys) rs140852238
NM_000208.4(INSR):c.1610+23C>T rs9676400
NM_000208.4(INSR):c.1610+28A>C rs2860177
NM_000208.4(INSR):c.1638C>T (p.Asp546=) rs2229429
NM_000208.4(INSR):c.1650G>A (p.Ala550=) rs2059806
NM_000208.4(INSR):c.1861+27C>T rs3815902
NM_000208.4(INSR):c.1862-20A>G rs2245648
NM_000208.4(INSR):c.1862-4A>G rs2245649
NM_000208.4(INSR):c.190T>C (p.Leu64=) rs144836032
NM_000208.4(INSR):c.1918C>T (p.Leu640=) rs2963
NM_000208.4(INSR):c.1932A>C (p.Pro644=) rs2245655
NM_000208.4(INSR):c.2117C>A (p.Ala706Asp) rs142391704
NM_000208.4(INSR):c.2193G>A (p.Thr731=) rs6413501
NM_000208.4(INSR):c.2231+20C>A rs6413502
NM_000208.4(INSR):c.2243C>T (p.Ser748Leu) rs143523271
NM_000208.4(INSR):c.225C>T (p.Asp75=) rs41352749
NM_000208.4(INSR):c.2267+17C>T rs41509747
NM_000208.4(INSR):c.2293G>A (p.Gly765Ser) rs146698985
NM_000208.4(INSR):c.2295C>T (p.Gly765=) rs142654992
NM_000208.4(INSR):c.2355G>A (p.Ser785=) rs148137322
NM_000208.4(INSR):c.2595C>T (p.Asn865=) rs2229431
NM_000208.4(INSR):c.2598C>T (p.Val866=) rs797045625
NM_000208.4(INSR):c.262T>C (p.Leu88=) rs61736580
NM_000208.4(INSR):c.2736G>A (p.Arg912=) rs147125937
NM_000208.4(INSR):c.2774T>C (p.Ile925Thr) rs1599881881
NM_000208.4(INSR):c.2838C>G (p.Asp946Glu) rs146588336
NM_000208.4(INSR):c.2842+33G>A rs35169098
NM_000208.4(INSR):c.2843-5T>G rs1555736265
NM_000208.4(INSR):c.2971C>A (p.Leu991Ile) rs150114699
NM_000208.4(INSR):c.3033C>T (p.Tyr1011=) rs1799815
NM_000208.4(INSR):c.3034G>A (p.Val1012Met) rs1799816
NM_000208.4(INSR):c.3164C>T (p.Ala1055Val) rs1599874183
NM_000208.4(INSR):c.3255C>T (p.His1085=) rs1799817
NM_000208.4(INSR):c.3259-31C>T rs148813626
NM_000208.4(INSR):c.3410T>C (p.Ile1137Thr) rs775854644
NM_000208.4(INSR):c.3668G>A (p.Gly1223Asp) rs1555734564
NM_000208.4(INSR):c.3775G>A (p.Asp1259Asn) rs369102740
NM_000208.4(INSR):c.421C>T (p.Arg141Trp) rs1555689823
NM_000208.4(INSR):c.5C>G (p.Ala2Gly) rs7508518
NM_000208.4(INSR):c.653-23TC[11] rs3835070
NM_000208.4(INSR):c.653-23TC[8] rs3835070
NM_000208.4(INSR):c.653-23TC[9] rs3835070
NM_000208.4(INSR):c.653-5_653-4insTC rs1555746859
NM_000208.4(INSR):c.653-7_653-6insTC rs1555746860
NM_000208.4(INSR):c.653-9_653-7delinsC rs1568470641
NM_000208.4(INSR):c.687C>T (p.Thr229=) rs150568177
NM_000208.4(INSR):c.728G>A (p.Cys243Tyr) rs911809758
NM_000208.4(INSR):c.783C>T (p.Asp261=) rs891087
NM_000208.4(INSR):c.84C>A (p.His28Gln) rs755298967
NM_000208.4(INSR):c.870C>T (p.His290=) rs74483718
NM_000208.4(INSR):c.959C>T (p.Thr320Met) rs138528064

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