ClinVar Miner

List of variants in gene FANCM studied for Hereditary breast ovarian cancer syndrome

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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_020937.4(FANCM):c.2996C>T (p.Pro999Leu) rs148304968 0.00044
NM_020937.4(FANCM):c.4709G>A (p.Arg1570His) rs201803784 0.00016
NM_020937.4(FANCM):c.1741C>T (p.Arg581Cys) rs202171930 0.00014
NM_020937.4(FANCM):c.5026G>A (p.Glu1676Lys) rs769919966 0.00006
NM_020937.4(FANCM):c.2311G>A (p.Glu771Lys) rs760204880 0.00004
NM_020937.4(FANCM):c.2240A>G (p.His747Arg) rs181827583 0.00003
NM_020937.4(FANCM):c.2444C>T (p.Ser815Leu) rs371688801 0.00002
NM_020937.4(FANCM):c.2696G>A (p.Arg899Lys) rs755241883 0.00001
NM_020937.4(FANCM):c.424C>T (p.Pro142Ser) rs771875070 0.00001
NM_020937.4(FANCM):c.4793A>G (p.Asp1598Gly) rs1405769485 0.00001
NM_020937.4(FANCM):c.1025G>A (p.Arg342Lys) rs1886815609
NM_020937.4(FANCM):c.173T>G (p.Leu58Arg) rs1885482402
NM_020937.4(FANCM):c.2201_2202dup (p.Glu735fs) rs762570903
NM_020937.4(FANCM):c.2525_2528del (p.Gln842fs) rs752136594
NM_020937.4(FANCM):c.3931C>T (p.Pro1311Ser) rs143997277
NM_020937.4(FANCM):c.4378A>C (p.Ile1460Leu) rs78211950
NM_020937.4(FANCM):c.4396T>A (p.Ser1466Thr) rs762757612
NM_020937.4(FANCM):c.4771T>A (p.Phe1591Ile) rs773152045
NM_020937.4(FANCM):c.4859AAG[2] (p.Glu1622del) rs765421461
NM_020937.4(FANCM):c.5068G>C (p.Val1690Leu) rs752352756
NM_020937.4(FANCM):c.5282C>T (p.Pro1761Leu) rs1395216158
NM_020937.4(FANCM):c.5306A>G (p.Gln1769Arg) rs1889621092
NM_020937.4(FANCM):c.5872G>T (p.Gly1958Cys) rs1441113303
NM_020937.4(FANCM):c.6008+1G>A rs984955481

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