ClinVar Miner

List of variants in gene INSR reported as uncertain significance

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Gene type:
ClinVar version:
Total variants: 205
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HGVS dbSNP
GRCh37/hg19 19p13.2(chr19:7129708-7296452)x1
GRCh37/hg19 19p13.2(chr19:7184327-7184648)x1
NM_000208.4(INSR):c.*1001A>G
NM_000208.4(INSR):c.*1045C>T
NM_000208.4(INSR):c.*1067G>A
NM_000208.4(INSR):c.*1137A>G
NM_000208.4(INSR):c.*1190A>G
NM_000208.4(INSR):c.*1191T>C rs564677377
NM_000208.4(INSR):c.*12G>A rs375751275
NM_000208.4(INSR):c.*1525G>A rs886054674
NM_000208.4(INSR):c.*1573C>T
NM_000208.4(INSR):c.*1574G>A
NM_000208.4(INSR):c.*1584C>G
NM_000208.4(INSR):c.*1591C>T
NM_000208.4(INSR):c.*1592G>A rs886054673
NM_000208.4(INSR):c.*1831C>A
NM_000208.4(INSR):c.*1831C>T
NM_000208.4(INSR):c.*1909A>G
NM_000208.4(INSR):c.*1917G>C
NM_000208.4(INSR):c.*1967G>A rs886054672
NM_000208.4(INSR):c.*2023A>G
NM_000208.4(INSR):c.*2102T>C
NM_000208.4(INSR):c.*2136T>A rs886054671
NM_000208.4(INSR):c.*2145_*2146dup rs57473640
NM_000208.4(INSR):c.*2149C>T rs886054670
NM_000208.4(INSR):c.*214G>A
NM_000208.4(INSR):c.*2160G>T rs570523460
NM_000208.4(INSR):c.*2255T>G rs547131375
NM_000208.4(INSR):c.*2318G>A rs80330850
NM_000208.4(INSR):c.*2322G>A
NM_000208.4(INSR):c.*2405A>T rs886054669
NM_000208.4(INSR):c.*241G>A
NM_000208.4(INSR):c.*2464C>T rs181555180
NM_000208.4(INSR):c.*2475A>G
NM_000208.4(INSR):c.*2517A>G rs886054668
NM_000208.4(INSR):c.*2568G>A
NM_000208.4(INSR):c.*2633del rs532103296
NM_000208.4(INSR):c.*2752C>G
NM_000208.4(INSR):c.*2752C>T
NM_000208.4(INSR):c.*280G>A rs886054685
NM_000208.4(INSR):c.*2853T>C rs186288667
NM_000208.4(INSR):c.*289del rs886054684
NM_000208.4(INSR):c.*3008_*3009del rs1555733404
NM_000208.4(INSR):c.*3008del rs72149315
NM_000208.4(INSR):c.*3009del rs140355086
NM_000208.4(INSR):c.*3010del rs886054664
NM_000208.4(INSR):c.*3013C>G
NM_000208.4(INSR):c.*3019C>A
NM_000208.4(INSR):c.*302A>G
NM_000208.4(INSR):c.*3101C>G
NM_000208.4(INSR):c.*3298C>T rs184243377
NM_000208.4(INSR):c.*334C>T
NM_000208.4(INSR):c.*334del rs886054683
NM_000208.4(INSR):c.*3390_*3392CAA[4] rs886054663
NM_000208.4(INSR):c.*348_*355dup rs71177157
NM_000208.4(INSR):c.*349_*355dup rs71177157
NM_000208.4(INSR):c.*352_*355dup rs71177157
NM_000208.4(INSR):c.*355_*356del rs1491388964
NM_000208.4(INSR):c.*356G>T
NM_000208.4(INSR):c.*356_*357del rs1555733954
NM_000208.4(INSR):c.*358_*359insTTTTTT rs886054680
NM_000208.4(INSR):c.*3654G>A rs753611294
NM_000208.4(INSR):c.*3693G>A rs886054662
NM_000208.4(INSR):c.*3855C>G
NM_000208.4(INSR):c.*3858G>A
NM_000208.4(INSR):c.*3894G>A rs184154294
NM_000208.4(INSR):c.*4349C>T rs886054661
NM_000208.4(INSR):c.*4374G>A rs886054660
NM_000208.4(INSR):c.*4376G>C
NM_000208.4(INSR):c.*4379C>T rs886054659
NM_000208.4(INSR):c.*4380G>A
NM_000208.4(INSR):c.*442G>T
NM_000208.4(INSR):c.*4696T>C
NM_000208.4(INSR):c.*4712T>C
NM_000208.4(INSR):c.*4719dup rs543556010
NM_000208.4(INSR):c.*4736T>G rs886054658
NM_000208.4(INSR):c.*499G>T
NM_000208.4(INSR):c.*511del rs886054679
NM_000208.4(INSR):c.*541dup rs886054678
NM_000208.4(INSR):c.*613C>T rs779517721
NM_000208.4(INSR):c.*743A>G
NM_000208.4(INSR):c.*853A>C rs886054677
NM_000208.4(INSR):c.*87C>T
NM_000208.4(INSR):c.*926_*927insG rs886054676
NM_000208.4(INSR):c.*927_*928insG rs886054675
NM_000208.4(INSR):c.*959A>G
NM_000208.4(INSR):c.*973dup rs547421118
NM_000208.4(INSR):c.*97A>G
NM_000208.4(INSR):c.*999A>G rs372034184
NM_000208.4(INSR):c.-12G>C rs143135433
NM_000208.4(INSR):c.-62C>T
NM_000208.4(INSR):c.101-1G>A rs1568229439
NM_000208.4(INSR):c.1056G>A (p.Thr352=)
NM_000208.4(INSR):c.1084G>A (p.Val362Ile) rs72549237
NM_000208.4(INSR):c.1151A>G (p.Asn384Ser)
NM_000208.4(INSR):c.1179G>A (p.Gly393=) rs140573575
NM_000208.4(INSR):c.1195C>T (p.Arg399Ter) rs121913151
NM_000208.4(INSR):c.1284T>C (p.Tyr428=) rs794727776
NM_000208.4(INSR):c.1305A>G (p.Leu435=)
NM_000208.4(INSR):c.1433G>A (p.Arg478His) rs750676016
NM_000208.4(INSR):c.1459A>C (p.Lys487Gln)
NM_000208.4(INSR):c.14G>A (p.Gly5Asp) rs886054690
NM_000208.4(INSR):c.151G>A (p.Glu51Lys) rs140852238
NM_000208.4(INSR):c.1550A>G (p.Glu517Gly)
NM_000208.4(INSR):c.1628C>T (p.Thr543Met) rs767160876
NM_000208.4(INSR):c.1665T>C (p.Ser555=) rs149795690
NM_000208.4(INSR):c.169G>A (p.Glu57Lys) rs886044001
NM_000208.4(INSR):c.1741C>T (p.Arg581Trp) rs1555743340
NM_000208.4(INSR):c.1810C>T (p.Arg604Trp) rs777486535
NM_000208.4(INSR):c.1866C>T (p.Pro622=)
NM_000208.4(INSR):c.190T>C (p.Leu64=) rs144836032
NM_000208.4(INSR):c.1988C>T (p.Ala663Val)
NM_000208.4(INSR):c.2117C>A (p.Ala706Asp) rs142391704
NM_000208.4(INSR):c.2121C>T (p.Gly707=)
NM_000208.4(INSR):c.221G>A (p.Arg74Gln)
NM_000208.4(INSR):c.2243C>T (p.Ser748Leu) rs143523271
NM_000208.4(INSR):c.2245G>A (p.Gly749Ser) rs545885277
NM_000208.4(INSR):c.2256C>G (p.Ala752=) rs376497490
NM_000208.4(INSR):c.225C>T (p.Asp75=) rs41352749
NM_000208.4(INSR):c.2263C>T (p.Pro755Ser) rs148838377
NM_000208.4(INSR):c.2268-3C>T rs750201666
NM_000208.4(INSR):c.2276G>A (p.Arg759Gln)
NM_000208.4(INSR):c.2280A>G (p.Lys760=) rs373695282
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.2327C>T (p.Thr776Met) rs377048253
NM_000208.4(INSR):c.2355G>A (p.Ser785=) rs148137322
NM_000208.4(INSR):c.2380G>A (p.Glu794Lys)
NM_000208.4(INSR):c.2384_2387dup (p.Pro797fs) rs1568441899
NM_000208.4(INSR):c.2388G>C (p.Arg796Ser) rs78433961
NM_000208.4(INSR):c.2471C>T (p.Ala824Val) rs886054689
NM_000208.4(INSR):c.2498G>A (p.Arg833Gln) rs777565396
NM_000208.4(INSR):c.2522G>A (p.Ser841Asn)
NM_000208.4(INSR):c.2543-13C>T
NM_000208.4(INSR):c.2564G>A (p.Gly855Asp) rs201667363
NM_000208.4(INSR):c.2573C>T (p.Thr858Met) rs201466857
NM_000208.4(INSR):c.2596G>A (p.Val866Ile)
NM_000208.4(INSR):c.2598C>T (p.Val866=) rs797045625
NM_000208.4(INSR):c.2602C>T (p.His868Tyr)
NM_000208.4(INSR):c.261C>T (p.Tyr87=)
NM_000208.4(INSR):c.2665C>T (p.Arg889Trp) rs76077021
NM_000208.4(INSR):c.2666G>A (p.Arg889Gln) rs187282966
NM_000208.4(INSR):c.2682+7C>T
NM_000208.4(INSR):c.2698G>A (p.Val900Ile)
NM_000208.4(INSR):c.2736G>A (p.Arg912=) rs147125937
NM_000208.4(INSR):c.2739G>T (p.Leu913=)
NM_000208.4(INSR):c.2793G>A (p.Ala931=) rs111502197
NM_000208.4(INSR):c.2829C>T (p.Tyr943=)
NM_000208.4(INSR):c.2838C>G (p.Asp946Glu) rs146588336
NM_000208.4(INSR):c.2842+4A>T
NM_000208.4(INSR):c.2842+6T>A rs767138526
NM_000208.4(INSR):c.2843-5T>G rs1555736265
NM_000208.4(INSR):c.2848G>A (p.Val950Ile)
NM_000208.4(INSR):c.2853G>A (p.Pro951=) rs200564313
NM_000208.4(INSR):c.2933T>A (p.Phe978Tyr) rs886054688
NM_000208.4(INSR):c.2970G>A (p.Pro990=) rs41304772
NM_000208.4(INSR):c.3023G>C (p.Cys1008Ser)
NM_000208.4(INSR):c.3034G>A (p.Val1012Met) rs1799816
NM_000208.4(INSR):c.3042C>T (p.Asp1014=) rs369686949
NM_000208.4(INSR):c.3054G>A (p.Val1018=) rs886054687
NM_000208.4(INSR):c.3071C>T (p.Thr1024Ile) rs780301757
NM_000208.4(INSR):c.307T>C (p.Phe103Leu) rs1568229181
NM_000208.4(INSR):c.3111G>A (p.Val1037=) rs761203697
NM_000208.4(INSR):c.3143G>A (p.Gly1048Asp) rs200921389
NM_000208.4(INSR):c.3158G>A (p.Arg1053His) rs748109926
NM_000208.4(INSR):c.3165G>A (p.Ala1055=) rs201445608
NM_000208.4(INSR):c.3193C>G (p.Leu1065Val) rs56395521
NM_000208.4(INSR):c.3364G>A (p.Ala1122Thr) rs1250061465
NM_000208.4(INSR):c.3370-12T>G rs200201955
NM_000208.4(INSR):c.3383G>A (p.Arg1128His) rs202160383
NM_000208.4(INSR):c.3410T>C (p.Ile1137Thr) rs775854644
NM_000208.4(INSR):c.345C>T (p.Phe115=)
NM_000208.4(INSR):c.3501C>T (p.Val1167=)
NM_000208.4(INSR):c.3529+5G>A rs764083259
NM_000208.4(INSR):c.3571C>T (p.Arg1191Trp) rs886054686
NM_000208.4(INSR):c.3668G>A (p.Gly1223Asp) rs1555734564
NM_000208.4(INSR):c.3669C>T (p.Gly1223=) rs750713967
NM_000208.4(INSR):c.3775G>A (p.Asp1259Asn) rs369102740
NM_000208.4(INSR):c.3805A>T (p.Met1269Leu) rs375197837
NM_000208.4(INSR):c.3808C>T (p.Arg1270Cys)
NM_000208.4(INSR):c.3809G>A (p.Arg1270His) rs746000108
NM_000208.4(INSR):c.3844A>G (p.Thr1282Ala)
NM_000208.4(INSR):c.3863A>G (p.Asn1288Ser) rs756542405
NM_000208.4(INSR):c.3964G>C (p.Glu1322Gln)
NM_000208.4(INSR):c.39G>C (p.Pro13=) rs771984795
NM_000208.4(INSR):c.4028G>A (p.Arg1343Gln) rs753624268
NM_000208.4(INSR):c.4065C>A (p.Tyr1355Ter)
NM_000208.4(INSR):c.408G>A (p.Leu136=) rs1568229079
NM_000208.4(INSR):c.4133G>C (p.Arg1378Pro)
NM_000208.4(INSR):c.4139A>G (p.Asn1380Ser)
NM_000208.4(INSR):c.41T>C (p.Leu14Pro) rs745857330
NM_000208.4(INSR):c.421C>T (p.Arg141Trp) rs1555689823
NM_000208.4(INSR):c.474C>T (p.Ile158=)
NM_000208.4(INSR):c.575G>A (p.Gly192Asp) rs143919163
NM_000208.4(INSR):c.624A>G (p.Arg208=) rs759705666
NM_000208.4(INSR):c.653-23TC[12] rs3835070
NM_000208.4(INSR):c.653-5_653-4insTC rs1555746859
NM_000208.4(INSR):c.653-9T>C rs868296217
NM_000208.4(INSR):c.698T>G (p.Leu233Arg)
NM_000208.4(INSR):c.728G>A (p.Cys243Tyr) rs911809758
NM_000208.4(INSR):c.756C>T (p.Cys252=) rs769511771
NM_000208.4(INSR):c.783C>G (p.Asp261Glu)
NM_000208.4(INSR):c.84C>A (p.His28Gln) rs755298967
NM_000208.4(INSR):c.921CAA[2] (p.Asn309del) rs775724610
NM_000208.4(INSR):c.959C>T (p.Thr320Met) rs138528064

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