ClinVar Miner

List of variants in gene FREM2 reported by PreventionGenetics, part of Exact Sciences

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Total variants: 114
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HGVS dbSNP gnomAD frequency
NM_207361.6(FREM2):c.2233= (p.Pro745=) rs2496423 0.99994
NM_207361.6(FREM2):c.576G>A (p.Glu192=) rs1868464 0.99992
NM_207361.6(FREM2):c.6977C>T (p.Thr2326Ile) rs9548509 0.73365
NM_207361.6(FREM2):c.7398A>G (p.Thr2466=) rs9532292 0.39041
NM_207361.6(FREM2):c.2250C>T (p.Asp750=) rs41292755 0.07615
NM_207361.6(FREM2):c.5003G>A (p.Arg1668His) rs1868463 0.05268
NM_207361.6(FREM2):c.8226C>T (p.Ala2742=) rs17058710 0.02172
NM_207361.6(FREM2):c.6036C>T (p.Phe2012=) rs115455037 0.00893
NM_207361.6(FREM2):c.4901C>T (p.Thr1634Met) rs74781600 0.00872
NM_207361.6(FREM2):c.3753C>T (p.Ser1251=) rs78099370 0.00823
NM_207361.6(FREM2):c.6396C>T (p.Phe2132=) rs61745902 0.00525
NM_207361.6(FREM2):c.2600C>T (p.Thr867Ile) rs61995710 0.00520
NM_207361.6(FREM2):c.4031G>A (p.Arg1344His) rs143044921 0.00430
NM_207361.6(FREM2):c.4730T>C (p.Ile1577Thr) rs114798977 0.00408
NM_207361.6(FREM2):c.4726C>G (p.Pro1576Ala) rs116742938 0.00406
NM_207361.6(FREM2):c.8902G>A (p.Val2968Ile) rs116099212 0.00379
NM_207361.6(FREM2):c.4319C>A (p.Thr1440Lys) rs79048205 0.00348
NM_207361.6(FREM2):c.7335T>C (p.Gly2445=) rs141921562 0.00276
NM_207361.6(FREM2):c.2128C>T (p.Arg710Cys) rs41292753 0.00274
NM_207361.6(FREM2):c.9113T>C (p.Val3038Ala) rs114688149 0.00204
NM_207361.6(FREM2):c.595G>T (p.Ala199Ser) rs151296346 0.00134
NM_207361.6(FREM2):c.2740T>G (p.Cys914Gly) rs146685625 0.00127
NM_207361.6(FREM2):c.9038C>T (p.Thr3013Met) rs114400765 0.00118
NM_207361.6(FREM2):c.7429C>T (p.Arg2477Trp) rs143571375 0.00115
NM_207361.6(FREM2):c.5417G>A (p.Gly1806Asp) rs145208009 0.00101
NM_207361.6(FREM2):c.2367G>A (p.Pro789=) rs140101984 0.00095
NM_207361.6(FREM2):c.8671+14A>G rs182974545 0.00088
NM_207361.6(FREM2):c.1580C>T (p.Ser527Leu) rs139804851 0.00084
NM_207361.6(FREM2):c.9010G>A (p.Ala3004Thr) rs145461540 0.00084
NM_207361.6(FREM2):c.109C>T (p.Leu37Phe) rs183560588 0.00081
NM_207361.6(FREM2):c.177T>C (p.Gly59=) rs370018440 0.00079
NM_207361.6(FREM2):c.2823C>T (p.Pro941=) rs150154438 0.00079
NM_207361.6(FREM2):c.2133G>A (p.Met711Ile) rs115446826 0.00052
NM_207361.6(FREM2):c.7966A>T (p.Ile2656Phe) rs150007765 0.00035
NM_207361.6(FREM2):c.8196C>T (p.Ser2732=) rs151062281 0.00034
NM_207361.6(FREM2):c.2432G>A (p.Gly811Glu) rs147293913 0.00031
NM_207361.6(FREM2):c.2480A>C (p.Asn827Thr) rs190810317 0.00029
NM_207361.6(FREM2):c.9009C>T (p.Val3003=) rs145657148 0.00026
NM_207361.6(FREM2):c.5279C>T (p.Thr1760Met) rs114171443 0.00022
NM_207361.6(FREM2):c.1191C>T (p.Pro397=) rs199831729 0.00021
NM_207361.6(FREM2):c.9007-8C>T rs374741888 0.00021
NM_207361.6(FREM2):c.2987T>A (p.Val996Asp) rs138416277 0.00016
NM_207361.6(FREM2):c.9337A>G (p.Thr3113Ala) rs202106776 0.00014
NM_207361.6(FREM2):c.5767+8G>A rs372938184 0.00013
NM_207361.6(FREM2):c.6743-9C>T rs749834830 0.00013
NM_207361.6(FREM2):c.7332C>T (p.Asp2444=) rs773197293 0.00013
NM_207361.6(FREM2):c.4150C>T (p.His1384Tyr) rs192340937 0.00012
NM_207361.6(FREM2):c.6669A>G (p.Gln2223=) rs114333791 0.00012
NM_207361.6(FREM2):c.3143A>G (p.Asn1048Ser) rs115192563 0.00011
NM_207361.6(FREM2):c.6273G>A (p.Ala2091=) rs769687764 0.00011
NM_207361.6(FREM2):c.4702C>T (p.Leu1568=) rs558845582 0.00010
NM_207361.6(FREM2):c.5790G>A (p.Pro1930=) rs114346379 0.00010
NM_207361.6(FREM2):c.6333C>T (p.Gly2111=) rs116763572 0.00010
NM_207361.6(FREM2):c.4038G>A (p.Gly1346=) rs139044304 0.00009
NM_207361.6(FREM2):c.8160A>C (p.Pro2720=) rs200528879 0.00009
NM_207361.6(FREM2):c.6108C>T (p.Asp2036=) rs200508468 0.00006
NM_207361.6(FREM2):c.6807G>A (p.Ser2269=) rs752080876 0.00005
NM_207361.6(FREM2):c.383C>T (p.Pro128Leu) rs114864077 0.00004
NM_207361.6(FREM2):c.8509C>T (p.Pro2837Ser) rs766715445 0.00004
NM_207361.6(FREM2):c.111C>T (p.Leu37=) rs765770038 0.00001
NM_207361.6(FREM2):c.2608C>T (p.Gln870Ter) rs750020230 0.00001
NM_207361.6(FREM2):c.4674C>T (p.Val1558=) rs769015024 0.00001
NM_207361.6(FREM2):c.9184G>T (p.Ala3062Ser) rs140456319 0.00001
NM_207361.6(FREM2):c.1122T>A (p.Asp374Glu)
NM_207361.6(FREM2):c.176G>A (p.Gly59Asp) rs115327344
NM_207361.6(FREM2):c.1824G>T (p.Gly608=)
NM_207361.6(FREM2):c.1854C>G (p.Pro618=)
NM_207361.6(FREM2):c.1959G>T (p.Leu653=)
NM_207361.6(FREM2):c.2097C>G (p.Leu699=)
NM_207361.6(FREM2):c.2149C>T (p.Gln717Ter)
NM_207361.6(FREM2):c.2250C>A (p.Asp750Glu)
NM_207361.6(FREM2):c.2625C>T (p.Gly875=)
NM_207361.6(FREM2):c.2977dup (p.Glu993fs)
NM_207361.6(FREM2):c.3035_3040dup (p.Gly1012_Ser1013dup) rs570476408
NM_207361.6(FREM2):c.305G>C (p.Gly102Ala)
NM_207361.6(FREM2):c.3266A>T (p.His1089Leu)
NM_207361.6(FREM2):c.3297dup (p.Asp1100Ter)
NM_207361.6(FREM2):c.3909G>A (p.Thr1303=)
NM_207361.6(FREM2):c.4074T>C (p.Thr1358=)
NM_207361.6(FREM2):c.4329A>G (p.Leu1443=)
NM_207361.6(FREM2):c.4378A>G (p.Ile1460Val)
NM_207361.6(FREM2):c.4442C>T (p.Ser1481Phe)
NM_207361.6(FREM2):c.4575C>T (p.Ser1525=)
NM_207361.6(FREM2):c.4584T>C (p.Asp1528=)
NM_207361.6(FREM2):c.4629C>T (p.Val1543=)
NM_207361.6(FREM2):c.5208A>G (p.Leu1736=)
NM_207361.6(FREM2):c.5263+10C>T rs781240147
NM_207361.6(FREM2):c.5460C>G (p.Gly1820=)
NM_207361.6(FREM2):c.5538G>A (p.Glu1846=)
NM_207361.6(FREM2):c.5676C>T (p.Ser1892=)
NM_207361.6(FREM2):c.567C>T (p.Val189=) rs370371340
NM_207361.6(FREM2):c.5714G>A (p.Arg1905Lys)
NM_207361.6(FREM2):c.5767+5C>G
NM_207361.6(FREM2):c.5768-7C>T
NM_207361.6(FREM2):c.5790G>C (p.Pro1930=)
NM_207361.6(FREM2):c.5991A>G (p.Gln1997=)
NM_207361.6(FREM2):c.6078G>A (p.Val2026=)
NM_207361.6(FREM2):c.6273G>T (p.Ala2091=)
NM_207361.6(FREM2):c.6379+5G>A
NM_207361.6(FREM2):c.6506G>A (p.Gly2169Glu)
NM_207361.6(FREM2):c.6925+1G>T
NM_207361.6(FREM2):c.7301G>T (p.Arg2434Leu) rs775757680
NM_207361.6(FREM2):c.7365C>T (p.Phe2455=)
NM_207361.6(FREM2):c.7440C>T (p.Cys2480=)
NM_207361.6(FREM2):c.7520-3A>C
NM_207361.6(FREM2):c.7548T>G (p.Val2516=)
NM_207361.6(FREM2):c.7663G>T (p.Val2555Leu) rs200997496
NM_207361.6(FREM2):c.8055C>T (p.Pro2685=)
NM_207361.6(FREM2):c.8166T>C (p.Ala2722=)
NM_207361.6(FREM2):c.8280C>T (p.Pro2760=)
NM_207361.6(FREM2):c.8344_8345delinsA (p.Leu2782fs)
NM_207361.6(FREM2):c.87G>C (p.Arg29=)
NM_207361.6(FREM2):c.87GCT[8] (p.Leu38_Ser39insLeu)
NM_207361.6(FREM2):c.9441G>A (p.Pro3147=)

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