ClinVar Miner

List of variants in gene INSR reported as benign

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Gene type:
ClinVar version:
Total variants: 48
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HGVS dbSNP
NM_000208.3(INSR):c.*104A>G rs1051690
NM_000208.3(INSR):c.*1416delA rs3833238
NM_000208.3(INSR):c.*1494G>A rs3745550
NM_000208.3(INSR):c.*1974_*1975delAT rs148930499
NM_000208.3(INSR):c.*2010G>A rs55972112
NM_000208.3(INSR):c.*2779G>A rs3745551
NM_000208.3(INSR):c.*2793C>A rs9282760
NM_000208.3(INSR):c.*2854G>T rs1864193
NM_000208.3(INSR):c.*288delC rs35434645
NM_000208.3(INSR):c.*3592A>G rs75499056
NM_000208.3(INSR):c.*3623A>G rs77859571
NM_000208.3(INSR):c.*3857C>T rs114405975
NM_000208.3(INSR):c.*4186T>C rs1366600
NM_000208.3(INSR):c.*4195T>C rs1366601
NM_000208.3(INSR):c.*4218G>C rs10416396
NM_000208.3(INSR):c.*4270G>A rs74433419
NM_000208.3(INSR):c.*4422G>T rs12642
NM_000208.3(INSR):c.*4474C>T rs1052371
NM_000208.3(INSR):c.*4794T>C rs10415841
NM_000208.3(INSR):c.*4802C>T rs12150997
NM_000208.3(INSR):c.*784C>G rs1051651
NM_000208.3(INSR):c.*930dupA rs34045095
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.3795-5C>T rs78312382
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.653-9_653-7delTCTinsC
NM_000208.4(INSR):c.2007C>T (p.Phe669=) rs2962
NM_000208.4(INSR):c.2595C>T (p.Asn865=) rs2229431
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.1918C>T (p.Leu640=) rs2963
NM_001079817.2(INSR):c.1932A>C (p.Pro644=) rs2245655
NM_001079817.2(INSR):c.2231+20C>A rs6413502
NM_001079817.2(INSR):c.2806+33G>A rs35169098
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.783C>T (p.Asp261=) rs891087
NM_001079817.2(INSR):c.870C>T (p.His290=) rs74483718

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