ClinVar Miner

List of variants in gene INSR studied for not provided

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Gene type:
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Total variants: 109
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HGVS dbSNP
GRCh37/hg19 19p13.2(chr19:7184327-7184648)x1
NM_000208.4(INSR):c.101-1G>A rs1568229439
NM_000208.4(INSR):c.1050G>A (p.Ser350=) rs751541632
NM_000208.4(INSR):c.1080C>T (p.Cys360=) rs56066516
NM_000208.4(INSR):c.1084G>A (p.Val362Ile) rs72549237
NM_000208.4(INSR):c.1092C>T (p.Asn364=) rs779479343
NM_000208.4(INSR):c.1098T>C (p.Ser366=) rs2229435
NM_000208.4(INSR):c.1179G>A (p.Gly393=) rs140573575
NM_000208.4(INSR):c.1179G>T (p.Gly393=) rs140573575
NM_000208.4(INSR):c.1191C>T (p.Ile397=) rs56135071
NM_000208.4(INSR):c.1195C>T (p.Arg399Ter) rs121913151
NM_000208.4(INSR):c.1203C>T (p.Tyr401=) rs76262811
NM_000208.4(INSR):c.1268+5G>A rs762359047
NM_000208.4(INSR):c.1284T>C (p.Tyr428=) rs794727776
NM_000208.4(INSR):c.1348C>T (p.Gln450Ter)
NM_000208.4(INSR):c.1433G>A (p.Arg478His) rs750676016
NM_000208.4(INSR):c.1503A>G (p.Lys501=) rs9676819
NM_000208.4(INSR):c.151G>A (p.Glu51Lys) rs140852238
NM_000208.4(INSR):c.1536C>A (p.Ile512=) rs1599937292
NM_000208.4(INSR):c.1550A>G (p.Glu517Gly)
NM_000208.4(INSR):c.1566C>T (p.Pro522=) rs546462100
NM_000208.4(INSR):c.1573C>T (p.Arg525Ter) rs1599937180
NM_000208.4(INSR):c.1584G>A (p.Leu528=) rs145334760
NM_000208.4(INSR):c.1665T>C (p.Ser555=) rs149795690
NM_000208.4(INSR):c.1671G>A (p.Thr557=) rs752643772
NM_000208.4(INSR):c.169G>A (p.Glu57Lys) rs886044001
NM_000208.4(INSR):c.1810C>T (p.Arg604Trp) rs777486535
NM_000208.4(INSR):c.190T>C (p.Leu64=) rs144836032
NM_000208.4(INSR):c.1989G>A (p.Ala663=) rs36081066
NM_000208.4(INSR):c.2030-3C>T rs766758560
NM_000208.4(INSR):c.2193G>A (p.Thr731=) rs6413501
NM_000208.4(INSR):c.2243C>T (p.Ser748Leu) rs143523271
NM_000208.4(INSR):c.2250T>C (p.Thr750=) rs1599907812
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.2275C>T (p.Arg759Trp) rs752552480
NM_000208.4(INSR):c.2295C>T (p.Gly765=) rs142654992
NM_000208.4(INSR):c.2319C>T (p.Ala773=) rs766008607
NM_000208.4(INSR):c.2325C>T (p.Pro775=) rs746508034
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.2361C>T (p.Ser787=) rs751613599
NM_000208.4(INSR):c.2370G>A (p.Thr790=) rs16994210
NM_000208.4(INSR):c.2376G>A (p.Pro792=) rs529869522
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.2517C>T (p.Tyr839=) rs769481102
NM_000208.4(INSR):c.2575C>T (p.His859Tyr) rs149536206
NM_000208.4(INSR):c.262T>C (p.Leu88=) rs61736580
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+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.2793G>A (p.Ala931=) rs111502197
NM_000208.4(INSR):c.2799C>T (p.Asn933=) rs113446125
NM_000208.4(INSR):c.2838C>G (p.Asp946Glu) rs146588336
NM_000208.4(INSR):c.2929_2932del (p.Leu977fs) rs1555736246
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.3034G>A (p.Val1012Met) rs1799816
NM_000208.4(INSR):c.3042C>T (p.Asp1014=) rs369686949
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.309C>T (p.Phe103=) rs1600111692
NM_000208.4(INSR):c.3102C>T (p.Phe1034=) rs143521418
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.3174G>A (p.Thr1058=) rs141582849
NM_000208.4(INSR):c.3193C>G (p.Leu1065Val) rs56395521
NM_000208.4(INSR):c.3228G>A (p.Ser1076=) rs768764179
NM_000208.4(INSR):c.3297G>A (p.Thr1099=) rs781555854
NM_000208.4(INSR):c.3324C>T (p.His1108=) rs202111071
NM_000208.4(INSR):c.350_353del (p.Asn117fs) rs1347163319
NM_000208.4(INSR):c.3615G>A (p.Pro1205=) rs146546375
NM_000208.4(INSR):c.3694T>C (p.Leu1232=) rs1599866174
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.3809G>A (p.Arg1270His) rs746000108
NM_000208.4(INSR):c.3863A>G (p.Asn1288Ser) rs756542405
NM_000208.4(INSR):c.3876C>T (p.Asp1292=) rs781656016
NM_000208.4(INSR):c.3964G>C (p.Glu1322Gln)
NM_000208.4(INSR):c.3999G>A (p.Ser1333=) rs746489788
NM_000208.4(INSR):c.3999G>T (p.Ser1333=) rs746489788
NM_000208.4(INSR):c.408G>A (p.Leu136=) rs1568229079
NM_000208.4(INSR):c.4134G>C (p.Arg1378=) rs763796481
NM_000208.4(INSR):c.41T>C (p.Leu14Pro) rs745857330
NM_000208.4(INSR):c.489C>A (p.Ile163=) rs530955658
NM_000208.4(INSR):c.575G>A (p.Gly192Asp) rs143919163
NM_000208.4(INSR):c.618C>T (p.Val206=) rs56012021
NM_000208.4(INSR):c.624A>G (p.Arg208=) rs759705666
NM_000208.4(INSR):c.653-23TC[14] rs3835070
NM_000208.4(INSR):c.653-23TC[16] rs3835070
NM_000208.4(INSR):c.653-23TC[20] rs3835070
NM_000208.4(INSR):c.653-23TC[8] rs3835070
NM_000208.4(INSR):c.653-7del rs766817873
NM_000208.4(INSR):c.653-9T>C rs868296217
NM_000208.4(INSR):c.653-9del rs754360103
NM_000208.4(INSR):c.687C>T (p.Thr229=) rs150568177
NM_000208.4(INSR):c.698T>G (p.Leu233Arg)
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.891G>A (p.Arg297=) rs1024295249
NM_000208.4(INSR):c.909G>A (p.Gln303=) rs9282757
NM_000208.4(INSR):c.936C>T (p.Ile312=) rs760555781
NM_000208.4(INSR):c.959C>T (p.Thr320Met) rs138528064

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