ClinVar Miner

List of variants in gene INSR reported as uncertain significance for Insulin-resistant diabetes mellitus AND acanthosis nigricans

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Gene type:
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Total variants: 53
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HGVS dbSNP
NM_000208.3(INSR):c.653-7_653-4dupTCTC rs3835070
NM_000208.4(INSR):c.*1525G>A rs886054674
NM_000208.4(INSR):c.*1592G>A rs886054673
NM_000208.4(INSR):c.*1967G>A rs886054672
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.*2405A>T rs886054669
NM_000208.4(INSR):c.*2517A>G rs886054668
NM_000208.4(INSR):c.*2633del rs532103296
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.*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.*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.*4349C>T rs886054661
NM_000208.4(INSR):c.*4374G>A rs886054660
NM_000208.4(INSR):c.*4379C>T rs886054659
NM_000208.4(INSR):c.*4719dup rs543556010
NM_000208.4(INSR):c.*4736T>G rs886054658
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.*853A>C rs886054677
NM_000208.4(INSR):c.*926_*927insG rs886054676
NM_000208.4(INSR):c.*927_*928insG rs886054675
NM_000208.4(INSR):c.*973dup rs547421118
NM_000208.4(INSR):c.*999A>G rs372034184
NM_000208.4(INSR):c.14G>A (p.Gly5Asp) rs886054690
NM_000208.4(INSR):c.1628C>T (p.Thr543Met) rs767160876
NM_000208.4(INSR):c.2268-3C>T rs750201666
NM_000208.4(INSR):c.2471C>T (p.Ala824Val) rs886054689
NM_000208.4(INSR):c.2573C>T (p.Thr858Met) rs201466857
NM_000208.4(INSR):c.2933T>A (p.Phe978Tyr) rs886054688
NM_000208.4(INSR):c.3054G>A (p.Val1018=) rs886054687
NM_000208.4(INSR):c.3143G>A (p.Gly1048Asp) rs200921389
NM_000208.4(INSR):c.3571C>T (p.Arg1191Trp) rs886054686
NM_000208.4(INSR):c.3669C>T (p.Gly1223=) rs750713967
NM_000208.4(INSR):c.4028G>A (p.Arg1343Gln) rs753624268
NM_000208.4(INSR):c.41T>C (p.Leu14Pro) rs745857330
NM_000208.4(INSR):c.756C>T (p.Cys252=) rs769511771

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