ClinVar Miner

List of variants in gene FMN1 reported by Eurofins NTD LLC (GA)

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_001277313.2(FMN1):c.3714+12T>C rs173224 0.65169
NM_001277313.2(FMN1):c.2717C>T (p.Pro906Leu) rs117804335 0.03499
NM_001277313.2(FMN1):c.2826T>G (p.Pro942=) rs74012406 0.02663
NM_001277313.2(FMN1):c.2652A>G (p.Gly884=) rs61739379 0.02473
NM_001277313.2(FMN1):c.2462A>G (p.Lys821Arg) rs61732708 0.02366
NM_001277313.2(FMN1):c.2374G>A (p.Asp792Asn) rs61736694 0.01476
NM_001277313.2(FMN1):c.2929G>A (p.Glu977Lys) rs150962800 0.01444
NM_001277313.2(FMN1):c.2044-1818A>G rs74655292 0.00784
NM_001277313.2(FMN1):c.2752A>G (p.Ser918Gly) rs57378148 0.00693
NM_001277313.2(FMN1):c.2614C>T (p.Pro872Ser) rs77531455 0.00363
NM_001277313.2(FMN1):c.2583A>G (p.Ala861=) rs61740952 0.00310
NM_001277313.2(FMN1):c.2697T>C (p.Ala899=) rs377621176 0.00310
NM_001277313.2(FMN1):c.2044-1683C>T rs73378526 0.00270
NM_001277313.2(FMN1):c.2044-2701C>A rs111822533 0.00226
NM_001277313.2(FMN1):c.3001C>T (p.Pro1001Ser) rs199592529 0.00205
NM_001277313.2(FMN1):c.4051G>A (p.Val1351Met) rs76835557 0.00136
NM_001277313.2(FMN1):c.3271G>A (p.Ala1091Thr) rs139446870 0.00123
NM_001277313.2(FMN1):c.2314G>A (p.Glu772Lys) rs144234543 0.00082
NM_001277313.2(FMN1):c.3974A>G (p.Gln1325Arg) rs147769257 0.00078
NM_001277313.2(FMN1):c.2044-1437T>C rs200868344 0.00077
NM_001277313.2(FMN1):c.2718G>A (p.Pro906=) rs370019638 0.00077
NM_001277313.2(FMN1):c.2044-1493G>T rs201555719 0.00073
NM_001277313.2(FMN1):c.2044-2686C>T rs202063843 0.00065
NM_001277313.2(FMN1):c.2044-1461G>A rs183013008 0.00063
NM_001277313.2(FMN1):c.2949G>A (p.Lys983=) rs80089865 0.00062
NM_001277313.2(FMN1):c.2044-2284C>T rs138694930 0.00038
NM_001277313.2(FMN1):c.2044-1807C>T rs199944520 0.00034
NM_001277313.2(FMN1):c.3528C>T (p.Ser1176=) rs369636169 0.00016
NM_001277313.2(FMN1):c.2044-1910A>G rs375235978 0.00014
NM_001277313.2(FMN1):c.2044-1924C>T rs201609721 0.00011
NM_001277313.2(FMN1):c.2044-1533T>G rs200018358 0.00009
NM_001277313.2(FMN1):c.2071G>C (p.Asp691His) rs1331356865 0.00006
NM_001277313.2(FMN1):c.2562C>G (p.Leu854=) rs200081244 0.00006
NM_001277313.2(FMN1):c.2799C>T (p.Ser933=) rs765680279 0.00005
NM_001277313.2(FMN1):c.3110C>T (p.Thr1037Ile) rs199988791 0.00004
NM_001277313.2(FMN1):c.2044-1917T>A rs754767298 0.00001
NM_001277313.2(FMN1):c.2044-2757A>G rs794726894 0.00001
NM_001277313.2(FMN1):c.3708T>C (p.Tyr1236=) rs370853923 0.00001
NM_001277313.2(FMN1):c.2044-1579G>A rs369308582
NM_001277313.2(FMN1):c.2044-1788C>T rs202171796
NM_001277313.2(FMN1):c.2517C>A (p.Ser839Arg) rs866847726
NM_001277313.2(FMN1):c.3139-10C>A rs200905611
NM_001277313.2(FMN1):c.3343GAA[2] (p.Glu1117del) rs535428264
NM_001277313.2(FMN1):c.4030_4032del (p.Lys1344del) rs145013933

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