ClinVar Miner

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

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Total variants: 34
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HGVS dbSNP
NM_000208.4(INSR):c.101-1G>A rs1568229439
NM_000208.4(INSR):c.1084G>A (p.Val362Ile) rs72549237
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.1433G>A (p.Arg478His) rs750676016
NM_000208.4(INSR):c.151G>A (p.Glu51Lys) rs140852238
NM_000208.4(INSR):c.1665T>C (p.Ser555=)
NM_000208.4(INSR):c.169G>A (p.Glu57Lys) rs886044001
NM_000208.4(INSR):c.1810C>T (p.Arg604Trp)
NM_000208.4(INSR):c.190T>C (p.Leu64=) rs144836032
NM_000208.4(INSR):c.2243C>T (p.Ser748Leu) rs143523271
NM_000208.4(INSR):c.2256C>G (p.Ala752=)
NM_000208.4(INSR):c.2327C>T (p.Thr776Met)
NM_000208.4(INSR):c.2384_2387dup (p.Pro797fs) rs1568441899
NM_000208.4(INSR):c.2498G>A (p.Arg833Gln) rs777565396
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.2736G>A (p.Arg912=) rs147125937
NM_000208.4(INSR):c.2838C>G (p.Asp946Glu) rs146588336
NM_000208.4(INSR):c.2970G>A (p.Pro990=) rs41304772
NM_000208.4(INSR):c.3042C>T (p.Asp1014=)
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.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.3805A>T (p.Met1269Leu) rs375197837
NM_000208.4(INSR):c.3863A>G (p.Asn1288Ser)
NM_000208.4(INSR):c.408G>A (p.Leu136=) rs1568229079
NM_000208.4(INSR):c.41T>C (p.Leu14Pro) rs745857330
NM_000208.4(INSR):c.653-9T>C
NM_000208.4(INSR):c.959C>T (p.Thr320Met) rs138528064

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