ClinVar Miner

List of variants in gene FANCM reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_020937.4(FANCM):c.5791C>T (p.Arg1931Ter) rs144567652 0.00088
NM_020937.4(FANCM):c.2859A>C (p.Lys953Asn) rs142864437 0.00064
NM_020937.4(FANCM):c.2996C>T (p.Pro999Leu) rs148304968 0.00044
NM_020937.4(FANCM):c.269C>T (p.Pro90Leu) rs142904668 0.00032
NM_020937.4(FANCM):c.1597C>T (p.Arg533Cys) rs146151355 0.00029
NM_020937.4(FANCM):c.3235A>T (p.Ser1079Cys) rs146065064 0.00026
NM_020937.4(FANCM):c.4627C>T (p.Leu1543Phe) rs139536545 0.00020
NM_020937.4(FANCM):c.5284C>A (p.Pro1762Thr) rs376197752 0.00015
NM_020937.4(FANCM):c.5832G>T (p.Leu1944Phe) rs201017015 0.00012
NM_020937.4(FANCM):c.4523C>G (p.Ala1508Gly) rs561723791 0.00009
NM_020937.4(FANCM):c.547A>C (p.Ser183Arg) rs368937236 0.00009
NM_020937.4(FANCM):c.1706G>A (p.Arg569His) rs754308821 0.00003
NM_020937.4(FANCM):c.3407T>C (p.Leu1136Ser) rs770989272 0.00003
NM_020937.4(FANCM):c.2244A>G (p.Gln748=) rs751605791 0.00001
NM_020937.4(FANCM):c.5681T>C (p.Ile1894Thr) rs1308170151 0.00001
NM_020937.4(FANCM):c.6129A>T (p.Arg2043Ser) rs772632630 0.00001
NM_020937.4(FANCM):c.1658_1660del (p.Gly553del) rs866897480
NM_020937.4(FANCM):c.174T>G (p.Leu58=) rs1178326678
NM_020937.4(FANCM):c.2258A>G (p.Asp753Gly) rs756438082
NM_020937.4(FANCM):c.3037A>G (p.Lys1013Glu) rs1888643453
NM_020937.4(FANCM):c.3490A>C (p.Lys1164Gln)
NM_020937.4(FANCM):c.36G>T (p.Trp12Cys) rs2139099472
NM_020937.4(FANCM):c.4005A>G (p.Lys1335=) rs1888735204
NM_020937.4(FANCM):c.5068G>A (p.Val1690Ile) rs752352756
NM_020937.4(FANCM):c.5107C>G (p.His1703Asp) rs367653310
NM_020937.4(FANCM):c.5196A>T (p.Lys1732Asn) rs2139297724
NM_020937.4(FANCM):c.5219A>G (p.Asp1740Gly) rs2139297887
NM_020937.4(FANCM):c.5434C>A (p.Pro1812Thr) rs3736772

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