ClinVar Miner

List of variants in gene FANCM reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_020937.4(FANCM):c.527C>T (p.Thr176Ile) rs77374493 0.00371
NM_020937.4(FANCM):c.5577T>C (p.Asn1859=) rs113831595 0.00300
NM_020937.4(FANCM):c.4260C>T (p.Asp1420=) rs113819179 0.00254
NM_020937.4(FANCM):c.171G>C (p.Leu57Phe) rs142007602 0.00161
NM_020937.4(FANCM):c.2268C>A (p.Arg756=) rs146061601 0.00128
NM_020937.4(FANCM):c.2859A>C (p.Lys953Asn) rs142864437 0.00064
NM_020937.4(FANCM):c.5067G>A (p.Ala1689=) rs148900115 0.00051
NM_020937.4(FANCM):c.4366C>T (p.Arg1456Cys) rs200360968 0.00027
NM_020937.4(FANCM):c.30G>A (p.Gln10=) rs145745979 0.00014
NM_020937.4(FANCM):c.4776G>A (p.Ser1592=) rs964884247 0.00005
NM_020937.4(FANCM):c.3513T>C (p.Pro1171=) rs771150480 0.00002
NM_020937.4(FANCM):c.2721T>G (p.Ala907=) rs150172333 0.00001
NM_020937.4(FANCM):c.4464C>T (p.Asn1488=) rs376583120 0.00001
NM_020937.4(FANCM):c.4465G>A (p.Gly1489Arg) rs183784665 0.00001
NM_020937.4(FANCM):c.1648T>C (p.Leu550=) rs776733099
NM_020937.4(FANCM):c.3297T>G (p.Arg1099=)
NM_020937.4(FANCM):c.4161T>C (p.Ser1387=)
NM_020937.4(FANCM):c.4839T>A (p.Ser1613=)
NM_020937.4(FANCM):c.5628T>C (p.Asn1876=) rs1039452790
NM_020937.4(FANCM):c.876G>T (p.Pro292=) rs150757891

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