ClinVar Miner

List of variants in gene INSR reported as benign

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Gene type:
ClinVar version:
Total variants: 91
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HGVS dbSNP
NM_000208.3(INSR):c.*4794T>C rs10415841
NM_000208.3(INSR):c.*4802C>T rs12150997
NM_000208.4(INSR):c.*104A>G rs1051690
NM_000208.4(INSR):c.*1089A>G rs116422284
NM_000208.4(INSR):c.*1416del rs3833238
NM_000208.4(INSR):c.*1432C>T rs111557734
NM_000208.4(INSR):c.*1494G>A rs3745550
NM_000208.4(INSR):c.*1974_*1975del rs148930499
NM_000208.4(INSR):c.*2010G>A rs55972112
NM_000208.4(INSR):c.*224C>T rs2860171
NM_000208.4(INSR):c.*2340A>G rs78987925
NM_000208.4(INSR):c.*2502A>G rs149795309
NM_000208.4(INSR):c.*2519G>A rs114982195
NM_000208.4(INSR):c.*2779G>A rs3745551
NM_000208.4(INSR):c.*2793C>A rs9282760
NM_000208.4(INSR):c.*2854G>T rs1864193
NM_000208.4(INSR):c.*288del rs35434645
NM_000208.4(INSR):c.*3029T>C rs72988602
NM_000208.4(INSR):c.*3463A>G rs115358150
NM_000208.4(INSR):c.*3541C>T rs116953519
NM_000208.4(INSR):c.*3592A>G rs75499056
NM_000208.4(INSR):c.*3623A>G rs77859571
NM_000208.4(INSR):c.*3786G>C
NM_000208.4(INSR):c.*3857C>T rs114405975
NM_000208.4(INSR):c.*4186T>C rs1366600
NM_000208.4(INSR):c.*4195T>C rs1366601
NM_000208.4(INSR):c.*4218G>C rs10416396
NM_000208.4(INSR):c.*4270G>A rs74433419
NM_000208.4(INSR):c.*4422G>T rs12642
NM_000208.4(INSR):c.*4474C>T rs1052371
NM_000208.4(INSR):c.*4602C>T rs10413914
NM_000208.4(INSR):c.*784C>G rs1051651
NM_000208.4(INSR):c.*930dup rs34045095
NM_000208.4(INSR):c.1080C>T (p.Cys360=) rs56066516
NM_000208.4(INSR):c.1098T>C (p.Ser366=) rs2229435
NM_000208.4(INSR):c.1123+13G>T rs72549236
NM_000208.4(INSR):c.1123+21G>A rs13306458
NM_000208.4(INSR):c.1179G>T (p.Gly393=) rs140573575
NM_000208.4(INSR):c.1483+31T>C rs2860178
NM_000208.4(INSR):c.1503A>G (p.Lys501=) rs9676819
NM_000208.4(INSR):c.1584G>A (p.Leu528=) rs145334760
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.1918C>T (p.Leu640=) rs2963
NM_000208.4(INSR):c.1932A>C (p.Pro644=) rs2245655
NM_000208.4(INSR):c.1989G>A (p.Ala663=) rs36081066
NM_000208.4(INSR):c.2007C>T (p.Phe669=) rs2962
NM_000208.4(INSR):c.2193G>A (p.Thr731=) rs6413501
NM_000208.4(INSR):c.2231+20C>A rs6413502
NM_000208.4(INSR):c.2267+17C>T rs41509747
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.2370G>A (p.Thr790=) rs16994210
NM_000208.4(INSR):c.2388G>C (p.Arg796Ser) rs78433961
NM_000208.4(INSR):c.2448G>A (p.Thr816=) rs2229434
NM_000208.4(INSR):c.2526G>C (p.Ala842=) rs2229430
NM_000208.4(INSR):c.2542+3A>G rs13306451
NM_000208.4(INSR):c.2595C>T (p.Asn865=) rs2229431
NM_000208.4(INSR):c.262T>C (p.Leu88=) rs61736580
NM_000208.4(INSR):c.2643C>T (p.Ile881=) rs2229432
NM_000208.4(INSR):c.2682+9C>G rs41398545
NM_000208.4(INSR):c.2683-5C>T rs41306363
NM_000208.4(INSR):c.2718T>C (p.Ala906=) rs2229433
NM_000208.4(INSR):c.2736G>A (p.Arg912=) rs147125937
NM_000208.4(INSR):c.2842+33G>A rs35169098
NM_000208.4(INSR):c.2970G>A (p.Pro990=) rs41304772
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.3255C>T (p.His1085=) rs1799817
NM_000208.4(INSR):c.3259-31C>T rs148813626
NM_000208.4(INSR):c.3795-5C>T rs78312382
NM_000208.4(INSR):c.489C>A (p.Ile163=) rs530955658
NM_000208.4(INSR):c.5C>G (p.Ala2Gly) rs7508518
NM_000208.4(INSR):c.618C>T (p.Val206=) rs56012021
NM_000208.4(INSR):c.653-23TC[11] rs3835070
NM_000208.4(INSR):c.653-23TC[14] rs3835070
NM_000208.4(INSR):c.653-23TC[8] rs3835070
NM_000208.4(INSR):c.653-23TC[9] rs3835070
NM_000208.4(INSR):c.653-7del rs766817873
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.783C>T (p.Asp261=) rs891087
NM_000208.4(INSR):c.870C>T (p.His290=) rs74483718
NM_000208.4(INSR):c.888G>A (p.Ser296=) rs2229428
NM_000208.4(INSR):c.909G>A (p.Gln303=) rs9282757

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