ClinVar Miner

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

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Gene type:
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Total variants: 48
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HGVS dbSNP
NM_000208.4(INSR):c.1050G>A (p.Ser350=) rs751541632
NM_000208.4(INSR):c.1092C>T (p.Asn364=) rs779479343
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.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.2030-3C>T rs766758560
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.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.2575C>T (p.His859Tyr) rs149536206
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.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.3615G>A (p.Pro1205=) rs146546375
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.4134G>C (p.Arg1378=) rs763796481
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.653-9del rs754360103
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

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