ClinVar Miner

List of variants in gene FREM1 studied for not specified

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Total variants: 29
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HGVS dbSNP gnomAD frequency
NM_001379081.2(FREM1):c.4791T>C (p.Asp1597=) rs1032474 0.85601
NM_001379081.2(FREM1):c.6428A>C (p.Gln2143Pro) rs10961689 0.74114
NM_001379081.2(FREM1):c.829-12A>G rs2818940 0.72914
NM_001379081.2(FREM1):c.1315G>C (p.Val439Leu) rs2779500 0.56393
NM_001379081.2(FREM1):c.4785C>T (p.Ala1595=) rs10733289 0.50486
NM_001379081.2(FREM1):c.5004C>A (p.Ile1668=) rs17219005 0.34768
NM_001379081.2(FREM1):c.3634G>T (p.Ala1212Ser) rs35870000 0.27977
NM_001379081.2(FREM1):c.4857+8T>C rs1874108 0.19884
NM_001379081.2(FREM1):c.2408C>A (p.Ser803Tyr) rs7023244 0.19696
NM_001379081.2(FREM1):c.3089-4G>T rs10810249 0.18577
NM_001379081.2(FREM1):c.3657A>G (p.Ala1219=) rs10738380 0.17766
NM_001379081.2(FREM1):c.4617G>A (p.Ala1539=) rs2131880 0.14595
NM_001379081.2(FREM1):c.5859T>C (p.Val1953=) rs4741426 0.14468
NM_001379081.2(FREM1):c.2587C>G (p.Leu863Val) rs7041710 0.12780
NM_001379081.2(FREM1):c.3819T>A (p.Asp1273Glu) rs7025814 0.06135
NM_001379081.2(FREM1):c.4466G>A (p.Arg1489Gln) rs61732355 0.01493
NM_001379081.2(FREM1):c.4727A>T (p.Asn1576Ile) rs2101770 0.00620
NM_001379081.2(FREM1):c.3575G>A (p.Arg1192His) rs79023327 0.00551
NM_001379081.2(FREM1):c.2274C>A (p.Gly758=) rs12235714 0.00497
NM_001379081.2(FREM1):c.4711G>A (p.Asp1571Asn) rs115421185 0.00244
NM_001379081.2(FREM1):c.3485A>G (p.Gln1162Arg) rs113555227 0.00160
NM_001379081.2(FREM1):c.1464C>T (p.Ser488=) rs200064797 0.00155
NM_001379081.2(FREM1):c.3147C>T (p.Ser1049=) rs200894045 0.00092
NM_001379081.2(FREM1):c.5622G>C (p.Trp1874Cys) rs61745612 0.00087
NM_001379081.2(FREM1):c.4499A>T (p.Glu1500Val) rs281875280 0.00038
NM_001379081.2(FREM1):c.4412G>A (p.Ser1471Asn) rs200650442 0.00025
NM_001379081.2(FREM1):c.1394G>C (p.Gly465Ala) rs41298151
NM_001379081.2(FREM1):c.3236C>T (p.Ser1079Phe)
NM_001379081.2(FREM1):c.5335-11dup rs140882884

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