ClinVar Miner

List of variants in gene INSR reported as uncertain significance for not specified

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Gene type:
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Total variants: 18
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NM_000208.4(INSR):c.1084G>A (p.Val362Ile) rs72549237
NM_000208.4(INSR):c.1151A>G (p.Asn384Ser)
NM_000208.4(INSR):c.151G>A (p.Glu51Lys) rs140852238
NM_000208.4(INSR):c.2243C>T (p.Ser748Leu) rs143523271
NM_000208.4(INSR):c.2293G>A (p.Gly765Ser) rs146698985
NM_000208.4(INSR):c.2355G>A (p.Ser785=) rs148137322
NM_000208.4(INSR):c.2598C>T (p.Val866=) rs797045625
NM_000208.4(INSR):c.2736G>A (p.Arg912=) rs147125937
NM_000208.4(INSR):c.2838C>G (p.Asp946Glu) rs146588336
NM_000208.4(INSR):c.2843-5T>G rs1555736265
NM_000208.4(INSR):c.3034G>A (p.Val1012Met) rs1799816
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.653-5_653-4insTC rs1555746859
NM_000208.4(INSR):c.728G>A (p.Cys243Tyr) rs911809758
NM_000208.4(INSR):c.84C>A (p.His28Gln) rs755298967

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