ClinVar Miner

List of variants in gene INSR reported as likely benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 87
Download table as spreadsheet
HGVS dbSNP
NM_000208.3(INSR):c.*4803G>A rs138569451
NM_000208.4(INSR):c.*1116G>A rs146905190
NM_000208.4(INSR):c.*1171C>T rs188386673
NM_000208.4(INSR):c.*1192G>A rs142596192
NM_000208.4(INSR):c.*130A>T
NM_000208.4(INSR):c.*1799C>T rs147080388
NM_000208.4(INSR):c.*1870C>G rs41315072
NM_000208.4(INSR):c.*2014C>T rs556567528
NM_000208.4(INSR):c.*2456C>T rs145777450
NM_000208.4(INSR):c.*2565C>T rs117532686
NM_000208.4(INSR):c.*2820G>A rs139376149
NM_000208.4(INSR):c.*3359G>A rs146249924
NM_000208.4(INSR):c.*3365C>A rs561270909
NM_000208.4(INSR):c.*3685T>C rs143409422
NM_000208.4(INSR):c.*3877T>C rs148660410
NM_000208.4(INSR):c.*394del rs140291876
NM_000208.4(INSR):c.*4760G>A rs574836227
NM_000208.4(INSR):c.*498_*499insTT rs71775166
NM_000208.4(INSR):c.*501T>G rs562228680
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.1092C>T (p.Asn364=) rs779479343
NM_000208.4(INSR):c.1123+13G>T rs72549236
NM_000208.4(INSR):c.1179G>A (p.Gly393=) rs140573575
NM_000208.4(INSR):c.1191C>T (p.Ile397=) rs56135071
NM_000208.4(INSR):c.1203C>T (p.Tyr401=) rs76262811
NM_000208.4(INSR):c.1268+5G>A rs762359047
NM_000208.4(INSR):c.1513A>G (p.Ile505Val) rs1599937384
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.1566C>T (p.Pro522=) rs546462100
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.190T>C (p.Leu64=) rs144836032
NM_000208.4(INSR):c.2030-3C>T rs766758560
NM_000208.4(INSR):c.2117C>A (p.Ala706Asp) rs142391704
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.224A>G (p.Asp75Gly)
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.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.2361C>T (p.Ser787=) rs751613599
NM_000208.4(INSR):c.2376G>A (p.Pro792=) rs529869522
NM_000208.4(INSR):c.2517C>T (p.Tyr839=) rs769481102
NM_000208.4(INSR):c.2572A>G (p.Thr858Ala) rs182552223
NM_000208.4(INSR):c.2575C>T (p.His859Tyr) rs149536206
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.2946-14T>C rs138585749
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.309C>T (p.Phe103=) rs1600111692
NM_000208.4(INSR):c.3102C>T (p.Phe1034=) rs143521418
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.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.3370-15G>A rs41300628
NM_000208.4(INSR):c.3615G>A (p.Pro1205=) rs146546375
NM_000208.4(INSR):c.3661T>G (p.Ser1221Ala) rs201979105
NM_000208.4(INSR):c.3694T>C (p.Leu1232=) rs1599866174
NM_000208.4(INSR):c.3876C>T (p.Asp1292=) rs781656016
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.4082A>G (p.Tyr1361Cys) rs13306449
NM_000208.4(INSR):c.4134G>C (p.Arg1378=) rs763796481
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.624A>G (p.Arg208=) rs759705666
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.653-7_653-6insTC rs1555746860
NM_000208.4(INSR):c.653-9del rs754360103
NM_000208.4(INSR):c.687C>T (p.Thr229=) rs150568177
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.936C>T (p.Ile312=) rs760555781
NM_000208.4(INSR):c.959C>T (p.Thr320Met) rs138528064

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.