ClinVar Miner

List of variants in gene INSR reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 144
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HGVS dbSNP gnomAD frequency
NM_000208.4(INSR):c.653-9del rs754360103 0.01255
NM_000208.4(INSR):c.2683-5C>T rs41306363 0.00664
NM_000208.4(INSR):c.3370-15G>A rs41300628 0.00616
NM_000208.4(INSR):c.1123+13G>T rs72549236 0.00526
NM_000208.4(INSR):c.3034G>A (p.Val1012Met) rs1799816 0.00500
NM_000208.4(INSR):c.870C>T (p.His290=) rs74483718 0.00416
NM_000208.4(INSR):c.2193G>A (p.Thr731=) rs6413501 0.00350
NM_000208.4(INSR):c.2946-14T>C rs138585749 0.00347
NM_000208.4(INSR):c.2355G>A (p.Ser785=) rs148137322 0.00285
NM_000208.4(INSR):c.1080C>T (p.Cys360=) rs56066516 0.00183
NM_000208.4(INSR):c.2838C>G (p.Asp946Glu) rs146588336 0.00145
NM_000208.4(INSR):c.2736G>A (p.Arg912=) rs147125937 0.00134
NM_000208.4(INSR):c.2575C>T (p.His859Tyr) rs149536206 0.00123
NM_000208.4(INSR):c.2243C>T (p.Ser748Leu) rs143523271 0.00116
NM_000208.4(INSR):c.2793G>A (p.Ala931=) rs111502197 0.00088
NM_000208.4(INSR):c.959C>T (p.Thr320Met) rs138528064 0.00087
NM_000208.4(INSR):c.2970G>A (p.Pro990=) rs41304772 0.00085
NM_000208.4(INSR):c.2263C>T (p.Pro755Ser) rs148838377 0.00064
NM_000208.4(INSR):c.2295C>T (p.Gly765=) rs142654992 0.00058
NM_000208.4(INSR):c.2573C>T (p.Thr858Met) rs201466857 0.00048
NM_000208.4(INSR):c.*3359G>A rs146249924 0.00038
NM_000208.4(INSR):c.2388G>C (p.Arg796Ser) rs78433961 0.00036
NM_000208.4(INSR):c.151G>A (p.Glu51Lys) rs140852238 0.00035
NM_000208.4(INSR):c.1503A>G (p.Lys501=) rs9676819 0.00034
NM_000208.4(INSR):c.3530-15C>A rs201189144 0.00031
NM_000208.4(INSR):c.39G>C (p.Pro13=) rs771984795 0.00029
NM_000208.4(INSR):c.3258+16G>A rs372761756 0.00026
NM_000208.4(INSR):c.1179G>A (p.Gly393=) rs140573575 0.00025
NM_000208.4(INSR):c.888G>A (p.Ser296=) rs2229428 0.00024
NM_000208.4(INSR):c.2665C>T (p.Arg889Trp) rs76077021 0.00021
NM_000208.4(INSR):c.2698G>A (p.Val900Ile) rs144029037 0.00021
NM_000208.4(INSR):c.3615G>A (p.Pro1205=) rs146546375 0.00020
NM_000208.4(INSR):c.1191C>T (p.Ile397=) rs56135071 0.00015
NM_000208.4(INSR):c.3174G>A (p.Thr1058=) rs141582849 0.00015
NM_000208.4(INSR):c.3228G>A (p.Ser1076=) rs768764179 0.00014
NM_000208.4(INSR):c.690C>T (p.Ala230=) rs373720760 0.00014
NM_000208.4(INSR):c.3591G>C (p.Leu1197=) rs776228235 0.00012
NM_000208.4(INSR):c.225C>T (p.Asp75=) rs41352749 0.00011
NM_000208.4(INSR):c.2766C>T (p.Ser922=) rs145713001 0.00011
NM_000208.4(INSR):c.1665T>C (p.Ser555=) rs149795690 0.00010
NM_000208.4(INSR):c.894G>A (p.Arg298=) rs757999365 0.00010
NM_000208.4(INSR):c.2117C>A (p.Ala706Asp) rs142391704 0.00009
NM_000208.4(INSR):c.3102C>T (p.Phe1034=) rs143521418 0.00009
NM_000208.4(INSR):c.575G>A (p.Gly192Asp) rs143919163 0.00009
NM_000208.4(INSR):c.2256C>G (p.Ala752=) rs376497490 0.00008
NM_000208.4(INSR):c.2517C>T (p.Tyr839=) rs769481102 0.00008
NM_000208.4(INSR):c.2598C>T (p.Val866=) rs797045625 0.00008
NM_000208.4(INSR):c.2754G>A (p.Pro918=) rs148994508 0.00008
NM_000208.4(INSR):c.2829C>T (p.Tyr943=) rs376766937 0.00008
NM_000208.4(INSR):c.881A>G (p.Lys294Arg) rs201147780 0.00007
NM_000208.4(INSR):c.1092C>T (p.Asn364=) rs779479343 0.00006
NM_000208.4(INSR):c.1203C>T (p.Tyr401=) rs76262811 0.00006
NM_000208.4(INSR):c.1268+5G>A rs762359047 0.00006
NM_000208.4(INSR):c.2799C>T (p.Asn933=) rs113446125 0.00006
NM_000208.4(INSR):c.2853G>A (p.Pro951=) rs200564313 0.00006
NM_000208.4(INSR):c.2361C>T (p.Ser787=) rs751613599 0.00005
NM_000208.4(INSR):c.3143G>A (p.Gly1048Asp) rs200921389 0.00005
NM_000208.4(INSR):c.1566C>T (p.Pro522=) rs546462100 0.00004
NM_000208.4(INSR):c.1671G>A (p.Thr557=) rs752643772 0.00004
NM_000208.4(INSR):c.2376G>A (p.Pro792=) rs529869522 0.00004
NM_000208.4(INSR):c.1050G>A (p.Ser350=) rs751541632 0.00003
NM_000208.4(INSR):c.3876C>T (p.Asp1292=) rs781656016 0.00003
NM_000208.4(INSR):c.2030-3C>T rs766758560 0.00002
NM_000208.4(INSR):c.2319C>T (p.Ala773=) rs766008607 0.00002
NM_000208.4(INSR):c.261C>T (p.Tyr87=) rs145884847 0.00002
NM_000208.4(INSR):c.3324C>T (p.His1108=) rs202111071 0.00002
NM_000208.4(INSR):c.2325C>T (p.Pro775=) rs746508034 0.00001
NM_000208.4(INSR):c.3297G>A (p.Thr1099=) rs781555854 0.00001
NM_000208.4(INSR):c.3321T>C (p.Ala1107=) rs1337155856 0.00001
NM_000208.4(INSR):c.3501C>T (p.Val1167=) rs373794054 0.00001
NM_000208.4(INSR):c.3999G>A (p.Ser1333=) rs746489788 0.00001
NM_000208.4(INSR):c.474C>T (p.Ile158=) rs752803584 0.00001
NM_000208.4(INSR):c.624A>G (p.Arg208=) rs759705666 0.00001
NM_000208.4(INSR):c.*130A>T rs571448308
NM_000208.4(INSR):c.101-19T>C
NM_000208.4(INSR):c.1123+19G>A
NM_000208.4(INSR):c.1237C>T (p.Arg413Cys)
NM_000208.4(INSR):c.1245T>A (p.Ile415=)
NM_000208.4(INSR):c.1377C>G (p.Pro459=)
NM_000208.4(INSR):c.1536C>A (p.Ile512=) rs1599937292
NM_000208.4(INSR):c.15C>G (p.Gly5=)
NM_000208.4(INSR):c.1917T>C (p.Ile639=)
NM_000208.4(INSR):c.1988C>T (p.Ala663Val) rs201034510
NM_000208.4(INSR):c.2029+17G>T
NM_000208.4(INSR):c.2034G>A (p.Leu678=)
NM_000208.4(INSR):c.2084A>G (p.Gln695Arg)
NM_000208.4(INSR):c.2115G>A (p.Ser705=)
NM_000208.4(INSR):c.2184T>C (p.Phe728=)
NM_000208.4(INSR):c.2199G>A (p.Glu733=)
NM_000208.4(INSR):c.2214C>T (p.Asn738=)
NM_000208.4(INSR):c.2223C>T (p.Phe741=)
NM_000208.4(INSR):c.2250T>C (p.Thr750=) rs1599907812
NM_000208.4(INSR):c.2267+8T>A
NM_000208.4(INSR):c.2313G>A (p.Thr771=)
NM_000208.4(INSR):c.2328G>A (p.Thr776=)
NM_000208.4(INSR):c.2354C>T (p.Ser785Leu)
NM_000208.4(INSR):c.2362G>A (p.Val788Met)
NM_000208.4(INSR):c.2375C>T (p.Pro792Leu)
NM_000208.4(INSR):c.2542+17G>A
NM_000208.4(INSR):c.2543-9T>C
NM_000208.4(INSR):c.2574G>A (p.Thr858=)
NM_000208.4(INSR):c.2682+16C>G
NM_000208.4(INSR):c.2697C>T (p.Cys899=)
NM_000208.4(INSR):c.270C>T (p.Leu90=)
NM_000208.4(INSR):c.2775C>A (p.Ile925=) rs1423085867
NM_000208.4(INSR):c.2877C>T (p.Ile959=)
NM_000208.4(INSR):c.2946-15G>A
NM_000208.4(INSR):c.2946-20G>A
NM_000208.4(INSR):c.309C>T (p.Phe103=) rs1600111692
NM_000208.4(INSR):c.3165G>A (p.Ala1055=) rs201445608
NM_000208.4(INSR):c.3370-16C>G
NM_000208.4(INSR):c.3370-16C>T
NM_000208.4(INSR):c.3435C>T (p.Asp1145=)
NM_000208.4(INSR):c.3465T>C (p.Phe1155=)
NM_000208.4(INSR):c.3615G>C (p.Pro1205=)
NM_000208.4(INSR):c.3694T>C (p.Leu1232=) rs1599866174
NM_000208.4(INSR):c.3918C>T (p.Ser1306=)
NM_000208.4(INSR):c.3999G>T (p.Ser1333=) rs746489788
NM_000208.4(INSR):c.4044G>C (p.Ser1348=) rs551853926
NM_000208.4(INSR):c.4058G>A (p.Arg1353Gln)
NM_000208.4(INSR):c.4086A>G (p.Thr1362=)
NM_000208.4(INSR):c.4134G>C (p.Arg1378=) rs763796481
NM_000208.4(INSR):c.498C>T (p.Ser166=)
NM_000208.4(INSR):c.561G>A (p.Pro187=)
NM_000208.4(INSR):c.652+19G>T
NM_000208.4(INSR):c.653-23TC[11] rs3835070
NM_000208.4(INSR):c.653-23TC[12] rs3835070
NM_000208.4(INSR):c.653-23TC[13] rs3835070
NM_000208.4(INSR):c.653-23TC[15] rs3835070
NM_000208.4(INSR):c.653-23TC[16] rs3835070
NM_000208.4(INSR):c.653-23TC[19]
NM_000208.4(INSR):c.653-23TC[20] rs3835070
NM_000208.4(INSR):c.653-23TC[21]
NM_000208.4(INSR):c.653-23TC[5]
NM_000208.4(INSR):c.653-23TC[9] rs3835070
NM_000208.4(INSR):c.653-7T>C
NM_000208.4(INSR):c.653-9T>C rs868296217
NM_000208.4(INSR):c.741C>T (p.Asp247=)
NM_000208.4(INSR):c.891G>A (p.Arg297=) rs1024295249
NM_000208.4(INSR):c.936C>T (p.Ile312=) rs760555781
NM_000208.4(INSR):c.951C>T (p.Ser317=)
NM_000208.4(INSR):c.975-25CT[4]
NM_000208.4(INSR):c.975-25CT[7]
NM_000208.4(INSR):c.975-9C>T

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