ClinVar Miner

List of variants in gene FANCA reported as likely benign for not specified

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Total variants: 28
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HGVS dbSNP
NM_000135.4(FANCA):c.115A>C (p.Arg39=) rs17232091
NM_000135.4(FANCA):c.1359+10C>T rs34159559
NM_000135.4(FANCA):c.1359+123C>G rs17232609
NM_000135.4(FANCA):c.1471-12A>G rs9282684
NM_000135.4(FANCA):c.1620T>C (p.Ile540=) rs1200375986
NM_000135.4(FANCA):c.1626+15G>C rs886038246
NM_000135.4(FANCA):c.1626+16C>T rs1800333
NM_000135.4(FANCA):c.1626+29C>T rs1800334
NM_000135.4(FANCA):c.1826+12C>T rs183513839
NM_000135.4(FANCA):c.1830A>G (p.Ala610=) rs1800338
NM_000135.4(FANCA):c.1874G>C (p.Cys625Ser) rs139235751
NM_000135.4(FANCA):c.1928C>G (p.Pro643Arg) rs34592408
NM_000135.4(FANCA):c.2015-5C>T rs780349960
NM_000135.4(FANCA):c.2021C>T (p.Ser674Leu) rs17232973
NM_000135.4(FANCA):c.2216C>T (p.Pro739Leu) rs45441106
NM_000135.4(FANCA):c.2391G>A (p.Ala797=) rs147882314
NM_000135.4(FANCA):c.2574C>G (p.Ser858Arg) rs17233141
NM_000135.4(FANCA):c.2602-19G>C rs17233225
NM_000135.4(FANCA):c.3348+29C>T rs1800348
NM_000135.4(FANCA):c.3408+42G>A rs886038247
NM_000135.4(FANCA):c.342C>T (p.Ala114=) rs777989691
NM_000135.4(FANCA):c.3468G>A (p.Leu1156=) rs1057520822
NM_000135.4(FANCA):c.3538G>A (p.Val1180Met) rs372706571
NM_000135.4(FANCA):c.3591G>A (p.Leu1197=) rs55773634
NM_000135.4(FANCA):c.754G>A (p.Asp252Asn) rs111944585
NM_000135.4(FANCA):c.80-13C>T rs189841793
NM_000135.4(FANCA):c.857A>G (p.Gln286Arg) rs13336566
NM_000135.4(FANCA):c.918G>A (p.Thr306=) rs199634699

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