ClinVar Miner

List of variants in gene FANCM reported as likely benign by PreventionGenetics, part of Exact Sciences

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Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_020937.4(FANCM):c.2749A>G (p.Ile917Val) rs148871932 0.00268
NM_020937.4(FANCM):c.5808C>T (p.Ser1936=) rs142333130 0.00178
NM_020937.4(FANCM):c.491A>C (p.His164Pro) rs144278051 0.00176
NM_020937.4(FANCM):c.1041G>A (p.Pro347=) rs140998495 0.00147
NM_020937.4(FANCM):c.1576C>G (p.Leu526Val) rs144215747 0.00147
NM_020937.4(FANCM):c.4147T>G (p.Tyr1383Asp) rs144104545 0.00118
NM_020937.4(FANCM):c.926A>C (p.Glu309Ala) rs143006771 0.00091
NM_020937.4(FANCM):c.3296G>A (p.Arg1099His) rs139382267 0.00083
NM_020937.4(FANCM):c.2517T>G (p.Ile839Met) rs61744648 0.00076
NM_020937.4(FANCM):c.2859A>C (p.Lys953Asn) rs142864437 0.00064
NM_020937.4(FANCM):c.3681A>G (p.Leu1227=) rs61749475 0.00047
NM_020937.4(FANCM):c.159C>T (p.Asp53=) rs147559750 0.00046
NM_020937.4(FANCM):c.2127G>A (p.Gln709=) rs141452622 0.00039
NM_020937.4(FANCM):c.2267G>A (p.Arg756His) rs142763060 0.00020
NM_020937.4(FANCM):c.4709G>A (p.Arg1570His) rs201803784 0.00016
NM_020937.4(FANCM):c.30G>A (p.Gln10=) rs145745979 0.00014
NM_020937.4(FANCM):c.1396+10A>G rs371211104 0.00009
NM_020937.4(FANCM):c.1996A>G (p.Arg666Gly) rs78437454 0.00006
NM_020937.4(FANCM):c.2330A>G (p.Tyr777Cys) rs200173413 0.00006
NM_020937.4(FANCM):c.3096T>C (p.Asp1032=) rs199507375 0.00006
NM_020937.4(FANCM):c.523T>C (p.Ser175Pro) rs779858649 0.00005
NM_020937.4(FANCM):c.5409T>C (p.Ala1803=) rs141214060 0.00003
NM_020937.4(FANCM):c.2628T>C (p.Asp876=) rs374313777 0.00002
NM_020937.4(FANCM):c.3513T>C (p.Pro1171=) rs771150480 0.00002
NM_020937.4(FANCM):c.6099A>G (p.Gln2033=) rs757734261 0.00002
NM_020937.4(FANCM):c.840T>C (p.Tyr280=) rs777422576 0.00002
NM_020937.4(FANCM):c.111C>T (p.Ser37=) rs763486658 0.00001
NM_020937.4(FANCM):c.2002+5A>G rs1888042696 0.00001
NM_020937.4(FANCM):c.2745T>C (p.Asn915=) rs915093857 0.00001
NM_020937.4(FANCM):c.4905T>C (p.Phe1635=) rs886038662 0.00001
NM_020937.4(FANCM):c.2002+11T>C
NM_020937.4(FANCM):c.2212C>T (p.Leu738=) rs2139234741
NM_020937.4(FANCM):c.2859A>G (p.Lys953=) rs142864437
NM_020937.4(FANCM):c.3141G>A (p.Gln1047=)
NM_020937.4(FANCM):c.3321A>G (p.Ala1107=) rs2139247556
NM_020937.4(FANCM):c.3810T>C (p.Ser1270=)
NM_020937.4(FANCM):c.3879T>G (p.Thr1293=)
NM_020937.4(FANCM):c.4005A>G (p.Lys1335=) rs1888735204
NM_020937.4(FANCM):c.4308C>T (p.Asn1436=)
NM_020937.4(FANCM):c.4473C>T (p.Ala1491=)
NM_020937.4(FANCM):c.4623A>G (p.Ser1541=)
NM_020937.4(FANCM):c.5151G>A (p.Lys1717=)
NM_020937.4(FANCM):c.5889A>G (p.Thr1963=)
NM_020937.4(FANCM):c.6090T>C (p.Phe2030=)
NM_020937.4(FANCM):c.639T>C (p.Ile213=)

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