ClinVar Miner

List of variants in gene IGF1R reported as uncertain significance by Invitae

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Gene type:
ClinVar version:
Total variants: 152
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HGVS dbSNP gnomAD frequency
NM_000875.5(IGF1R):c.4058G>A (p.Arg1353His) rs149470389 0.00031
NM_000875.5(IGF1R):c.4069C>T (p.Arg1357Trp) rs143940675 0.00028
NM_000875.5(IGF1R):c.1679A>G (p.Lys560Arg) rs148974751 0.00014
NM_000875.5(IGF1R):c.850A>T (p.Asn284Tyr) rs144675711 0.00013
NM_000875.5(IGF1R):c.4066G>A (p.Glu1356Lys) rs746562843 0.00011
NM_000875.5(IGF1R):c.1963G>A (p.Gly655Ser) rs143193096 0.00010
NM_000875.5(IGF1R):c.4096A>C (p.Thr1366Pro) rs773129173 0.00010
NM_000875.5(IGF1R):c.2077G>A (p.Gly693Ser) rs375617925 0.00006
NM_000875.5(IGF1R):c.2258G>A (p.Arg753Gln) rs987303175 0.00006
NM_000875.5(IGF1R):c.3852G>T (p.Glu1284Asp) rs746049391 0.00005
NM_000875.5(IGF1R):c.1573G>A (p.Val525Ile) rs201778894 0.00004
NM_000875.5(IGF1R):c.2815G>A (p.Ala939Thr) rs755569322 0.00004
NM_000875.5(IGF1R):c.3979A>G (p.Asn1327Asp) rs374710491 0.00004
NM_000875.5(IGF1R):c.721G>A (p.Ala241Thr) rs775630539 0.00004
NM_000875.5(IGF1R):c.2042A>G (p.Glu681Gly) rs200059469 0.00002
NM_000875.5(IGF1R):c.1537C>T (p.Arg513Trp) rs760388654 0.00001
NM_000875.5(IGF1R):c.1868C>G (p.Ser623Cys) rs886051560 0.00001
NM_000875.5(IGF1R):c.3685G>A (p.Gly1229Ser) rs368518102 0.00001
NM_000875.5(IGF1R):c.3932C>T (p.Ser1311Leu) rs771642071 0.00001
NC_000015.9:g.(?_99192811)_(99251356_?)dup
NC_000015.9:g.(?_99434534)_(99505828_?)dup
NM_000875.5(IGF1R):c.100G>C (p.Gly34Arg)
NM_000875.5(IGF1R):c.1171C>T (p.Arg391Cys)
NM_000875.5(IGF1R):c.1217G>A (p.Arg406His)
NM_000875.5(IGF1R):c.1248-3T>C
NM_000875.5(IGF1R):c.1289A>G (p.Gln430Arg) rs2151670129
NM_000875.5(IGF1R):c.1299C>G (p.Asp433Glu)
NM_000875.5(IGF1R):c.1303G>A (p.Asp435Asn)
NM_000875.5(IGF1R):c.1321A>G (p.Ile441Val)
NM_000875.5(IGF1R):c.1338G>A (p.Met446Ile)
NM_000875.5(IGF1R):c.1372G>C (p.Glu458Gln)
NM_000875.5(IGF1R):c.1382G>A (p.Arg461His)
NM_000875.5(IGF1R):c.1412G>A (p.Arg471His)
NM_000875.5(IGF1R):c.1480C>T (p.His494Tyr)
NM_000875.5(IGF1R):c.1487C>T (p.Thr496Ile)
NM_000875.5(IGF1R):c.1513A>G (p.Ile505Val)
NM_000875.5(IGF1R):c.1519A>G (p.Ile507Val)
NM_000875.5(IGF1R):c.1531C>T (p.Arg511Trp)
NM_000875.5(IGF1R):c.1576T>C (p.Tyr526His)
NM_000875.5(IGF1R):c.1590-20_1590-19inv
NM_000875.5(IGF1R):c.1660G>A (p.Val554Met)
NM_000875.5(IGF1R):c.1670C>T (p.Pro557Leu)
NM_000875.5(IGF1R):c.1687G>A (p.Glu563Lys)
NM_000875.5(IGF1R):c.1693G>A (p.Gly565Ser)
NM_000875.5(IGF1R):c.1735G>A (p.Val579Ile)
NM_000875.5(IGF1R):c.1764G>T (p.Met588Ile)
NM_000875.5(IGF1R):c.1829-4C>T
NM_000875.5(IGF1R):c.1848C>T (p.Asp616=)
NM_000875.5(IGF1R):c.1882A>G (p.Ile628Val)
NM_000875.5(IGF1R):c.1885G>A (p.Val629Met)
NM_000875.5(IGF1R):c.1913A>G (p.Asn638Ser)
NM_000875.5(IGF1R):c.1915G>A (p.Gly639Ser)
NM_000875.5(IGF1R):c.1948C>T (p.Arg650Trp)
NM_000875.5(IGF1R):c.1964G>T (p.Gly655Val)
NM_000875.5(IGF1R):c.1975C>T (p.Arg659Trp)
NM_000875.5(IGF1R):c.2032A>G (p.Ile678Val)
NM_000875.5(IGF1R):c.212G>A (p.Arg71His)
NM_000875.5(IGF1R):c.2246C>T (p.Thr749Ile)
NM_000875.5(IGF1R):c.2265G>T (p.Arg755Ser)
NM_000875.5(IGF1R):c.2273C>T (p.Thr758Met)
NM_000875.5(IGF1R):c.2288A>G (p.Tyr763Cys)
NM_000875.5(IGF1R):c.2362A>G (p.Thr788Ala)
NM_000875.5(IGF1R):c.2363C>G (p.Thr788Ser)
NM_000875.5(IGF1R):c.2374A>G (p.Asn792Asp)
NM_000875.5(IGF1R):c.2425G>A (p.Glu809Lys)
NM_000875.5(IGF1R):c.2449G>A (p.Ala817Thr)
NM_000875.5(IGF1R):c.245C>T (p.Thr82Ile)
NM_000875.5(IGF1R):c.2485+3A>G
NM_000875.5(IGF1R):c.2486-3C>A rs2151693329
NM_000875.5(IGF1R):c.2494G>A (p.Asp832Asn)
NM_000875.5(IGF1R):c.2524C>T (p.Pro842Ser)
NM_000875.5(IGF1R):c.2542A>G (p.Ile848Val)
NM_000875.5(IGF1R):c.2579G>A (p.Gly860Glu) rs2151693458
NM_000875.5(IGF1R):c.2615A>G (p.Gln872Arg)
NM_000875.5(IGF1R):c.2649G>T (p.Gln883His)
NM_000875.5(IGF1R):c.2668G>A (p.Gly890Arg)
NM_000875.5(IGF1R):c.2693C>T (p.Pro898Leu)
NM_000875.5(IGF1R):c.2710C>T (p.Arg904Trp)
NM_000875.5(IGF1R):c.2786G>A (p.Gly929Glu)
NM_000875.5(IGF1R):c.2795A>G (p.Asn932Ser)
NM_000875.5(IGF1R):c.2824G>A (p.Val942Ile)
NM_000875.5(IGF1R):c.2827G>A (p.Ala943Thr)
NM_000875.5(IGF1R):c.2876A>G (p.His959Arg)
NM_000875.5(IGF1R):c.2882A>G (p.Lys961Arg)
NM_000875.5(IGF1R):c.2898G>T (p.Arg966Ser)
NM_000875.5(IGF1R):c.289G>A (p.Gly97Arg)
NM_000875.5(IGF1R):c.2962G>A (p.Val988Ile)
NM_000875.5(IGF1R):c.2969A>G (p.Asp990Gly)
NM_000875.5(IGF1R):c.296T>A (p.Leu99His)
NM_000875.5(IGF1R):c.3049G>T (p.Val1017Phe)
NM_000875.5(IGF1R):c.3064G>A (p.Val1022Met)
NM_000875.5(IGF1R):c.3094A>G (p.Ile1032Val)
NM_000875.5(IGF1R):c.3115G>A (p.Ala1039Thr)
NM_000875.5(IGF1R):c.3115G>T (p.Ala1039Ser)
NM_000875.5(IGF1R):c.3187-3C>T
NM_000875.5(IGF1R):c.320G>A (p.Arg107His)
NM_000875.5(IGF1R):c.3302A>C (p.Asn1101Thr)
NM_000875.5(IGF1R):c.3304C>T (p.Pro1102Ser)
NM_000875.5(IGF1R):c.3330C>G (p.Ser1110Arg)
NM_000875.5(IGF1R):c.3342G>T (p.Gln1114His)
NM_000875.5(IGF1R):c.3458-3C>T
NM_000875.5(IGF1R):c.3595G>A (p.Gly1199Arg) rs886044448
NM_000875.5(IGF1R):c.3616G>A (p.Ala1206Thr)
NM_000875.5(IGF1R):c.3676A>C (p.Met1226Leu)
NM_000875.5(IGF1R):c.3709T>A (p.Cys1237Ser)
NM_000875.5(IGF1R):c.370A>C (p.Asn124His)
NM_000875.5(IGF1R):c.3722+4C>T
NM_000875.5(IGF1R):c.3723-6C>T
NM_000875.5(IGF1R):c.3735G>A (p.Met1245Ile)
NM_000875.5(IGF1R):c.3736C>T (p.Arg1246Cys)
NM_000875.5(IGF1R):c.3751T>C (p.Tyr1251His)
NM_000875.5(IGF1R):c.3758C>A (p.Pro1253His)
NM_000875.5(IGF1R):c.3763A>G (p.Met1255Val) rs149148921
NM_000875.5(IGF1R):c.3785T>C (p.Ile1262Thr)
NM_000875.5(IGF1R):c.3786C>G (p.Ile1262Met)
NM_000875.5(IGF1R):c.3802GAG[1] (p.Glu1269del)
NM_000875.5(IGF1R):c.3811G>C (p.Glu1271Gln)
NM_000875.5(IGF1R):c.3814C>G (p.Pro1272Ala)
NM_000875.5(IGF1R):c.3823C>T (p.Arg1275Trp)
NM_000875.5(IGF1R):c.3824G>A (p.Arg1275Gln) rs556294716
NM_000875.5(IGF1R):c.3829G>A (p.Val1277Ile)
NM_000875.5(IGF1R):c.382A>G (p.Ile128Val)
NM_000875.5(IGF1R):c.3863C>T (p.Pro1288Leu)
NM_000875.5(IGF1R):c.3865G>A (p.Glu1289Lys)
NM_000875.5(IGF1R):c.3868C>G (p.Pro1290Ala)
NM_000875.5(IGF1R):c.3907G>A (p.Val1303Ile)
NM_000875.5(IGF1R):c.3935C>T (p.Ser1312Phe)
NM_000875.5(IGF1R):c.3943C>T (p.Pro1315Ser)
NM_000875.5(IGF1R):c.3952G>A (p.Asp1318Asn)
NM_000875.5(IGF1R):c.3962C>T (p.Ser1321Leu)
NM_000875.5(IGF1R):c.3986C>G (p.Pro1329Arg)
NM_000875.5(IGF1R):c.3988G>A (p.Gly1330Ser) rs200870187
NM_000875.5(IGF1R):c.4010G>A (p.Arg1337His)
NM_000875.5(IGF1R):c.4010G>T (p.Arg1337Leu)
NM_000875.5(IGF1R):c.4012G>A (p.Ala1338Thr)
NM_000875.5(IGF1R):c.4012G>C (p.Ala1338Pro)
NM_000875.5(IGF1R):c.4021G>A (p.Asp1341Asn)
NM_000875.5(IGF1R):c.404A>G (p.Asn135Ser)
NM_000875.5(IGF1R):c.4070G>A (p.Arg1357Gln)
NM_000875.5(IGF1R):c.4082T>G (p.Leu1361Arg)
NM_000875.5(IGF1R):c.515A>G (p.Asn172Ser)
NM_000875.5(IGF1R):c.526A>G (p.Lys176Glu)
NM_000875.5(IGF1R):c.607T>C (p.Tyr203His)
NM_000875.5(IGF1R):c.628C>T (p.Arg210Cys)
NM_000875.5(IGF1R):c.629G>A (p.Arg210His)
NM_000875.5(IGF1R):c.722C>T (p.Ala241Val)
NM_000875.5(IGF1R):c.728A>G (p.Asp243Gly)
NM_000875.5(IGF1R):c.736A>G (p.Thr246Ala)
NM_000875.5(IGF1R):c.784C>T (p.Pro262Ser)
NM_000875.5(IGF1R):c.854T>C (p.Ile285Thr)
NM_000875.5(IGF1R):c.929G>A (p.Gly310Asp)
NM_000875.5(IGF1R):c.943G>A (p.Gly315Ser)

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