ClinVar Miner

List of variants in gene FREM1 reported as likely benign by Invitae

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Gene type:
ClinVar version:
Total variants: 195
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HGVS dbSNP gnomAD frequency
NM_001379081.2(FREM1):c.4963G>A (p.Val1655Met) rs114410606 0.00315
NM_001379081.2(FREM1):c.5212C>A (p.Leu1738Met) rs138267253 0.00314
NM_001379081.2(FREM1):c.4711G>A (p.Asp1571Asn) rs115421185 0.00244
NM_001379081.2(FREM1):c.4564G>A (p.Val1522Met) rs61735747 0.00226
NM_001379081.2(FREM1):c.3485A>G (p.Gln1162Arg) rs113555227 0.00160
NM_001379081.2(FREM1):c.795C>A (p.Asp265Glu) rs140222993 0.00128
NM_001379081.2(FREM1):c.1184A>C (p.Glu395Ala) rs150070740 0.00126
NM_001379081.2(FREM1):c.4442+3G>A rs181859461 0.00119
NM_001379081.2(FREM1):c.1493G>A (p.Arg498Gln) rs184394424 0.00107
NM_001379081.2(FREM1):c.1520G>A (p.Arg507His) rs202115210 0.00089
NM_001379081.2(FREM1):c.5622G>C (p.Trp1874Cys) rs61745612 0.00087
NM_001379081.2(FREM1):c.3874C>T (p.Arg1292Cys) rs199806592 0.00078
NM_001379081.2(FREM1):c.3331C>T (p.His1111Tyr) rs200339767 0.00068
NM_001379081.2(FREM1):c.3631C>T (p.Pro1211Ser) rs76714828 0.00064
NM_001379081.2(FREM1):c.4867T>C (p.Leu1623=) rs369101934 0.00064
NM_001379081.2(FREM1):c.541C>T (p.Arg181Trp) rs200482899 0.00052
NM_001379081.2(FREM1):c.2169+11A>C rs377670533 0.00051
NM_001379081.2(FREM1):c.5448C>T (p.Asp1816=) rs374311778 0.00050
NM_001379081.2(FREM1):c.4995C>T (p.Asp1665=) rs372941168 0.00049
NM_001379081.2(FREM1):c.6465A>G (p.Gln2155=) rs368790874 0.00039
NM_001379081.2(FREM1):c.4945A>G (p.Ile1649Val) rs199891537 0.00030
NM_001379081.2(FREM1):c.6021C>G (p.Pro2007=) rs200987019 0.00030
NM_001379081.2(FREM1):c.4412G>A (p.Ser1471Asn) rs200650442 0.00025
NM_001379081.2(FREM1):c.3756A>G (p.Gln1252=) rs373197206 0.00022
NM_001379081.2(FREM1):c.546G>T (p.Leu182=) rs369937228 0.00019
NM_001379081.2(FREM1):c.3404T>C (p.Ile1135Thr) rs187388944 0.00016
NM_001379081.2(FREM1):c.2450G>A (p.Arg817Gln) rs200495440 0.00015
NM_001379081.2(FREM1):c.324T>A (p.Leu108=) rs781396064 0.00013
NM_001379081.2(FREM1):c.329+10A>C rs369341108 0.00013
NM_001379081.2(FREM1):c.3471+9C>T rs377668876 0.00013
NM_001379081.2(FREM1):c.3552G>A (p.Leu1184=) rs371506251 0.00011
NM_001379081.2(FREM1):c.5155G>A (p.Val1719Met) rs201617511 0.00011
NM_001379081.2(FREM1):c.6189C>T (p.Tyr2063=) rs779712053 0.00011
NM_001379081.2(FREM1):c.3340A>T (p.Ile1114Leu) rs369645961 0.00010
NM_001379081.2(FREM1):c.6222C>T (p.Thr2074=) rs370887201 0.00008
NM_001379081.2(FREM1):c.329+12G>A rs552377277 0.00007
NM_001379081.2(FREM1):c.2640+16C>G rs779202191 0.00006
NM_001379081.2(FREM1):c.3573A>G (p.Pro1191=) rs375774862 0.00006
NM_001379081.2(FREM1):c.3789C>T (p.Thr1263=) rs369457169 0.00006
NM_001379081.2(FREM1):c.4879G>T (p.Ala1627Ser) rs370198850 0.00006
NM_001379081.2(FREM1):c.4983T>A (p.Pro1661=) rs111333359 0.00006
NM_001379081.2(FREM1):c.1038T>C (p.Thr346=) rs773920119 0.00004
NM_001379081.2(FREM1):c.1882-14C>G rs201311456 0.00004
NM_001379081.2(FREM1):c.2226C>A (p.Pro742=) rs373535650 0.00004
NM_001379081.2(FREM1):c.3378A>G (p.Thr1126=) rs202213402 0.00004
NM_001379081.2(FREM1):c.3932T>C (p.Ile1311Thr) rs182527895 0.00004
NM_001379081.2(FREM1):c.4476C>T (p.His1492=) rs368796043 0.00004
NM_001379081.2(FREM1):c.246C>T (p.Cys82=) rs766485109 0.00003
NM_001379081.2(FREM1):c.4263C>T (p.Asp1421=) rs773027758 0.00003
NM_001379081.2(FREM1):c.5205-4A>G rs746001376 0.00003
NM_001379081.2(FREM1):c.329+7G>A rs180917208 0.00002
NM_001379081.2(FREM1):c.1053C>T (p.His351=) rs371463084 0.00001
NM_001379081.2(FREM1):c.2640+7A>G rs772475006 0.00001
NM_001379081.2(FREM1):c.3813T>A (p.Val1271=) rs745782166 0.00001
NM_001379081.2(FREM1):c.396T>C (p.Cys132=) rs1040244120 0.00001
NM_001379081.2(FREM1):c.4542G>C (p.Gly1514=) rs545742838 0.00001
NM_001379081.2(FREM1):c.4801C>A (p.Gln1601Lys) rs550726565 0.00001
NM_001379081.2(FREM1):c.1020G>A (p.Pro340=)
NM_001379081.2(FREM1):c.1104C>T (p.Ile368=)
NM_001379081.2(FREM1):c.1153-14_1153-13del
NM_001379081.2(FREM1):c.1173C>T (p.Asp391=)
NM_001379081.2(FREM1):c.1262-4A>G
NM_001379081.2(FREM1):c.1296C>T (p.Ile432=)
NM_001379081.2(FREM1):c.1320C>T (p.Val440=)
NM_001379081.2(FREM1):c.1325A>G (p.Asn442Ser)
NM_001379081.2(FREM1):c.1393+17G>T
NM_001379081.2(FREM1):c.1518C>T (p.Ile506=)
NM_001379081.2(FREM1):c.1539C>T (p.Asn513=)
NM_001379081.2(FREM1):c.1578C>A (p.Thr526=)
NM_001379081.2(FREM1):c.1875G>A (p.Val625=)
NM_001379081.2(FREM1):c.1875G>T (p.Val625=)
NM_001379081.2(FREM1):c.1902T>C (p.Thr634=)
NM_001379081.2(FREM1):c.2079-4T>G
NM_001379081.2(FREM1):c.2127A>G (p.Val709=)
NM_001379081.2(FREM1):c.2208C>T (p.Pro736=)
NM_001379081.2(FREM1):c.2212C>G (p.Gln738Glu) rs182946445
NM_001379081.2(FREM1):c.2223T>G (p.Gly741=)
NM_001379081.2(FREM1):c.2337+17A>G
NM_001379081.2(FREM1):c.2337+18T>C
NM_001379081.2(FREM1):c.234+10A>T
NM_001379081.2(FREM1):c.234+12C>T
NM_001379081.2(FREM1):c.2340G>T (p.Ala780=)
NM_001379081.2(FREM1):c.2385C>A (p.Ile795=)
NM_001379081.2(FREM1):c.2478G>A (p.Glu826=)
NM_001379081.2(FREM1):c.2547-15del
NM_001379081.2(FREM1):c.2604T>C (p.Asp868=) rs2130638517
NM_001379081.2(FREM1):c.2640+11A>C
NM_001379081.2(FREM1):c.2894-11G>T
NM_001379081.2(FREM1):c.2898C>T (p.Gly966=)
NM_001379081.2(FREM1):c.3021C>G (p.Ser1007=)
NM_001379081.2(FREM1):c.3045C>T (p.Ile1015=)
NM_001379081.2(FREM1):c.3088+18T>C
NM_001379081.2(FREM1):c.3093C>T (p.Pro1031=)
NM_001379081.2(FREM1):c.3114C>G (p.Gly1038=) rs765109399
NM_001379081.2(FREM1):c.3138C>T (p.Asn1046=)
NM_001379081.2(FREM1):c.3267A>C (p.Ile1089=)
NM_001379081.2(FREM1):c.329+11C>T
NM_001379081.2(FREM1):c.329+7G>T rs180917208
NM_001379081.2(FREM1):c.330-18G>T
NM_001379081.2(FREM1):c.3300C>T (p.Asn1100=)
NM_001379081.2(FREM1):c.3339G>A (p.Arg1113=)
NM_001379081.2(FREM1):c.3378A>T (p.Thr1126=)
NM_001379081.2(FREM1):c.3399G>A (p.Leu1133=)
NM_001379081.2(FREM1):c.3420A>T (p.Ile1140=)
NM_001379081.2(FREM1):c.342A>G (p.Arg114=)
NM_001379081.2(FREM1):c.3471+18A>G
NM_001379081.2(FREM1):c.3585C>T (p.Leu1195=)
NM_001379081.2(FREM1):c.3600G>C (p.Gly1200=)
NM_001379081.2(FREM1):c.3681A>G (p.Glu1227=)
NM_001379081.2(FREM1):c.36G>C (p.Val12=)
NM_001379081.2(FREM1):c.3723C>T (p.Asp1241=)
NM_001379081.2(FREM1):c.3802G>T (p.Val1268Phe) rs554857144
NM_001379081.2(FREM1):c.3839+11T>G
NM_001379081.2(FREM1):c.3839+17G>T
NM_001379081.2(FREM1):c.3981+7G>A
NM_001379081.2(FREM1):c.3982-22_3982-19del
NM_001379081.2(FREM1):c.4038G>T (p.Val1346=)
NM_001379081.2(FREM1):c.4056A>G (p.Arg1352=)
NM_001379081.2(FREM1):c.4068C>T (p.Thr1356=)
NM_001379081.2(FREM1):c.4119T>C (p.Asp1373=)
NM_001379081.2(FREM1):c.4128C>T (p.Asn1376=)
NM_001379081.2(FREM1):c.4177+11G>A
NM_001379081.2(FREM1):c.4178-17C>A
NM_001379081.2(FREM1):c.4206C>A (p.Leu1402=)
NM_001379081.2(FREM1):c.4326C>T (p.Ile1442=)
NM_001379081.2(FREM1):c.4353C>T (p.Pro1451=)
NM_001379081.2(FREM1):c.4365C>T (p.Phe1455=)
NM_001379081.2(FREM1):c.4392A>C (p.Thr1464=)
NM_001379081.2(FREM1):c.4410G>A (p.Lys1470=)
NM_001379081.2(FREM1):c.4413C>T (p.Ser1471=)
NM_001379081.2(FREM1):c.447C>G (p.Gly149=)
NM_001379081.2(FREM1):c.4482G>A (p.Val1494=)
NM_001379081.2(FREM1):c.4500G>A (p.Glu1500=) rs561131255
NM_001379081.2(FREM1):c.4578C>G (p.Ser1526=)
NM_001379081.2(FREM1):c.4599C>T (p.Thr1533=) rs540319616
NM_001379081.2(FREM1):c.4665C>G (p.Leu1555=)
NM_001379081.2(FREM1):c.4665C>T (p.Leu1555=)
NM_001379081.2(FREM1):c.4677G>A (p.Gly1559=)
NM_001379081.2(FREM1):c.4686A>G (p.Leu1562=)
NM_001379081.2(FREM1):c.4692A>G (p.Gln1564=)
NM_001379081.2(FREM1):c.4738C>T (p.Arg1580Trp)
NM_001379081.2(FREM1):c.483C>T (p.Phe161=) rs540878376
NM_001379081.2(FREM1):c.4848C>T (p.Phe1616=)
NM_001379081.2(FREM1):c.4858-17C>T
NM_001379081.2(FREM1):c.4962C>T (p.Arg1654=)
NM_001379081.2(FREM1):c.5028A>G (p.Pro1676=)
NM_001379081.2(FREM1):c.5059+18C>G
NM_001379081.2(FREM1):c.5157G>A (p.Val1719=)
NM_001379081.2(FREM1):c.5204+8C>G rs376644135
NM_001379081.2(FREM1):c.5205-5C>A
NM_001379081.2(FREM1):c.5232A>G (p.Glu1744=)
NM_001379081.2(FREM1):c.5244C>G (p.Thr1748=) rs150403611
NM_001379081.2(FREM1):c.5268G>A (p.Val1756=)
NM_001379081.2(FREM1):c.5313C>T (p.Asp1771=)
NM_001379081.2(FREM1):c.5316G>A (p.Ser1772=)
NM_001379081.2(FREM1):c.5316G>T (p.Ser1772=) rs775863172
NM_001379081.2(FREM1):c.5335-11T>C
NM_001379081.2(FREM1):c.5335-7T>C
NM_001379081.2(FREM1):c.5335-8C>A
NM_001379081.2(FREM1):c.5361A>G (p.Gly1787=)
NM_001379081.2(FREM1):c.5373C>T (p.Thr1791=)
NM_001379081.2(FREM1):c.5403C>T (p.Asp1801=)
NM_001379081.2(FREM1):c.5532A>G (p.Ala1844=) rs1249507655
NM_001379081.2(FREM1):c.5670T>C (p.Phe1890=) rs756654353
NM_001379081.2(FREM1):c.5796+19T>C
NM_001379081.2(FREM1):c.5797-7A>T
NM_001379081.2(FREM1):c.5800C>T (p.Arg1934Cys)
NM_001379081.2(FREM1):c.5808C>T (p.Ser1936=)
NM_001379081.2(FREM1):c.5877T>C (p.Asp1959=)
NM_001379081.2(FREM1):c.5892T>C (p.Thr1964=)
NM_001379081.2(FREM1):c.5934A>G (p.Gln1978=)
NM_001379081.2(FREM1):c.6010-11C>T
NM_001379081.2(FREM1):c.6039C>T (p.Cys2013=)
NM_001379081.2(FREM1):c.6138+14T>C
NM_001379081.2(FREM1):c.6138+15G>A
NM_001379081.2(FREM1):c.6139-15A>G
NM_001379081.2(FREM1):c.6144G>A (p.Val2048=)
NM_001379081.2(FREM1):c.6186C>T (p.Gly2062=)
NM_001379081.2(FREM1):c.6222C>G (p.Thr2074=)
NM_001379081.2(FREM1):c.6231G>A (p.Ala2077=) rs148735553
NM_001379081.2(FREM1):c.6231G>T (p.Ala2077=) rs148735553
NM_001379081.2(FREM1):c.624A>G (p.Pro208=)
NM_001379081.2(FREM1):c.632-11G>A
NM_001379081.2(FREM1):c.632-14G>A
NM_001379081.2(FREM1):c.6340+9C>T rs562121209
NM_001379081.2(FREM1):c.6408T>C (p.Asn2136=)
NM_001379081.2(FREM1):c.672C>G (p.Thr224=) rs1588406105
NM_001379081.2(FREM1):c.693A>G (p.Gly231=)
NM_001379081.2(FREM1):c.6C>T (p.Asn2=)
NM_001379081.2(FREM1):c.738T>C (p.Arg246=)
NM_001379081.2(FREM1):c.828+13G>A
NM_001379081.2(FREM1):c.828+15T>G
NM_001379081.2(FREM1):c.829-18T>C
NM_001379081.2(FREM1):c.873G>A (p.Pro291=)
NM_001379081.2(FREM1):c.897C>T (p.Phe299=)

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