ClinVar Miner

List of variants in gene FANCA studied for not specified

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Gene type:
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Total variants: 109
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HGVS dbSNP
NM_000135.2(FANCA):c.1084-29A>G rs6500452
NM_000135.2(FANCA):c.1084-49G>C rs1800287
NM_000135.2(FANCA):c.1143G>T (p.Thr381=) rs1800331
NM_000135.2(FANCA):c.115A>C (p.Arg39=) rs17232091
NM_000135.2(FANCA):c.1226-20A>G rs1800330
NM_000135.2(FANCA):c.1235C>T (p.Ala412Val) rs11646374
NM_000135.2(FANCA):c.1290G>A (p.Ala430=) rs1800332
NM_000135.2(FANCA):c.1359+10C>T rs34159559
NM_000135.2(FANCA):c.1359+123C>G rs17232609
NM_000135.2(FANCA):c.1471-12A>G rs9282684
NM_000135.2(FANCA):c.1501G>A (p.Gly501Ser) rs2239359
NM_000135.2(FANCA):c.1626+15G>C rs886038246
NM_000135.2(FANCA):c.1626+16C>T rs1800333
NM_000135.2(FANCA):c.1626+29C>T rs1800334
NM_000135.2(FANCA):c.1627-32T>C rs17226337
NM_000135.2(FANCA):c.1777-29T>C rs2302162
NM_000135.2(FANCA):c.1777-41_1777-38delTTTC rs56163653
NM_000135.2(FANCA):c.1826+12C>T rs183513839
NM_000135.2(FANCA):c.1826+15T>C rs1800337
NM_000135.2(FANCA):c.1826+30_1826+31insGT rs36204974
NM_000135.2(FANCA):c.1830A>G (p.Ala610=) rs1800338
NM_000135.2(FANCA):c.1874G>C (p.Cys625Ser) rs139235751
NM_000135.2(FANCA):c.1927C>G (p.Pro643Ala) rs17232910
NM_000135.2(FANCA):c.1928C>G (p.Pro643Arg) rs34592408
NM_000135.2(FANCA):c.1941G>A (p.Glu647=) rs17232917
NM_000135.2(FANCA):c.2015-5C>T rs780349960
NM_000135.2(FANCA):c.2021C>T (p.Ser674Leu) rs17232973
NM_000135.2(FANCA):c.2101A>G (p.Lys701Glu) rs56369086
NM_000135.2(FANCA):c.2151+8T>C rs1800340
NM_000135.2(FANCA):c.2151G>T (p.Met717Ile) rs1131660
NM_000135.2(FANCA):c.2216C>T (p.Pro739Leu) rs45441106
NM_000135.2(FANCA):c.2391G>A (p.Ala797=) rs147882314
NM_000135.2(FANCA):c.2426G>A (p.Gly809Asp) rs7195066
NM_000135.2(FANCA):c.2567T>C (p.Leu856Ser) rs370085403
NM_000135.2(FANCA):c.2574C>G (p.Ser858Arg) rs17233141
NM_000135.2(FANCA):c.2602-19G>C rs17233225
NM_000135.2(FANCA):c.2602-36G>T rs2159116
NM_000135.2(FANCA):c.2602-46T>A rs11076620
NM_000135.2(FANCA):c.2779-7T>C rs17233253
NM_000135.2(FANCA):c.2901C>T (p.Ser967=) rs17226980
NM_000135.2(FANCA):c.3067-23G>A rs17227057
NM_000135.2(FANCA):c.3067-4T>C rs17227064
NM_000135.2(FANCA):c.3240-42G>A rs1800345
NM_000135.2(FANCA):c.3263C>T (p.Ser1088Phe) rs17233497
NM_000135.2(FANCA):c.3348+18A>G rs1800347
NM_000135.2(FANCA):c.3348+29C>T rs1800348
NM_000135.2(FANCA):c.3408+33T>C rs17227191
NM_000135.2(FANCA):c.3408+42G>A rs886038247
NM_000135.2(FANCA):c.3408+45G>A rs1800355
NM_000135.2(FANCA):c.3412C>G (p.Leu1138Val) rs138417003
NM_000135.2(FANCA):c.3427C>G (p.Leu1143Val) rs61753269
NM_000135.2(FANCA):c.3430C>T (p.Arg1144Trp) rs143671872
NM_000135.2(FANCA):c.3468G>A (p.Leu1156=) rs1057520822
NM_000135.2(FANCA):c.3524C>T (p.Pro1175Leu) rs147017625
NM_000135.2(FANCA):c.3583C>T (p.Arg1195Trp) rs143642304
NM_000135.2(FANCA):c.3591G>A (p.Leu1197=) rs55773634
NM_000135.2(FANCA):c.3654A>G (p.Pro1218=) rs1800358
NM_000135.2(FANCA):c.3765+37G>A rs34420680
NM_000135.2(FANCA):c.377C>G (p.Thr126Arg) rs139160837
NM_000135.2(FANCA):c.427-25T>A rs9282685
NM_000135.2(FANCA):c.480G>A (p.Met160Ile) rs200603300
NM_000135.2(FANCA):c.542C>T (p.Ala181Val) rs17232246
NM_000135.2(FANCA):c.623C>T (p.Ser208Leu) rs144420697
NM_000135.2(FANCA):c.710-12A>G rs1800286
NM_000135.2(FANCA):c.755A>G (p.Asp252Gly) rs17225943
NM_000135.2(FANCA):c.793-9T>C rs757500718
NM_000135.2(FANCA):c.796A>G (p.Thr266Ala) rs7190823
NM_000135.2(FANCA):c.80-13C>T rs189841793
NM_000135.2(FANCA):c.827-156G>A rs797045571
NM_000135.2(FANCA):c.857A>G (p.Gln286Arg) rs13336566
NM_000135.2(FANCA):c.862G>T (p.Glu288Ter) rs148100796
NM_000135.2(FANCA):c.894-8A>G rs11648881
NM_000135.2(FANCA):c.918G>A (p.Thr306=) rs199634699
NM_000135.2(FANCA):c.932T>C (p.Ile311Thr) rs75501942
NM_000135.3(FANCA):c.1048C>T (p.Arg350Trp) rs150290184
NM_000135.3(FANCA):c.1049G>A (p.Arg350Gln) rs199967286
NM_000135.3(FANCA):c.1049G>T (p.Arg350Leu) rs199967286
NM_000135.3(FANCA):c.1226-2A>G rs773906241
NM_000135.3(FANCA):c.1245G>A (p.Met415Ile) rs1555561439
NM_000135.3(FANCA):c.1549C>T (p.Arg517Trp) rs587778309
NM_000135.3(FANCA):c.1620T>C (p.Ile540=) rs1200375986
NM_000135.3(FANCA):c.1625A>T (p.Glu542Val) rs587778310
NM_000135.3(FANCA):c.1811T>C (p.Ile604Thr) rs1555551989
NM_000135.3(FANCA):c.1861delT (p.Tyr621Thrfs) rs587778311
NM_000135.3(FANCA):c.2008C>T (p.Arg670Cys) rs587778312
NM_000135.3(FANCA):c.2072A>G (p.Asn691Ser) rs367880372
NM_000135.3(FANCA):c.2222+7G>A rs374312736
NM_000135.3(FANCA):c.2519C>G (p.Ala840Gly) rs587778313
NM_000135.3(FANCA):c.2568G>C (p.Leu856Phe) rs587778314
NM_000135.3(FANCA):c.2601+9A>T rs771837383
NM_000135.3(FANCA):c.2681G>A (p.Arg894Lys) rs587778316
NM_000135.3(FANCA):c.2706C>G (p.Asp902Glu) rs587778315
NM_000135.3(FANCA):c.2859C>A (p.Asp953Glu) rs149112292
NM_000135.3(FANCA):c.2942G>C (p.Cys981Ser) rs1555542910
NM_000135.3(FANCA):c.2944A>G (p.Thr982Ala) rs587778317
NM_000135.3(FANCA):c.2977C>A (p.Gln993Lys) rs140823801
NM_000135.3(FANCA):c.301C>G (p.Gln101Glu) rs140412064
NM_000135.3(FANCA):c.308C>T (p.Ser103Leu) rs147176389
NM_000135.3(FANCA):c.3422C>A (p.Ala1141Asp) rs587778318
NM_000135.3(FANCA):c.342C>T (p.Ala114=) rs777989691
NM_000135.3(FANCA):c.3538G>A (p.Val1180Met) rs372706571
NM_000135.3(FANCA):c.3584G>A (p.Arg1195Gln) rs138013482
NM_000135.3(FANCA):c.370A>T (p.Ile124Phe) rs553656166
NM_000135.3(FANCA):c.553C>A (p.Leu185Ile) rs587778323
NM_000135.3(FANCA):c.679C>G (p.His227Asp) rs142580507
NM_000135.3(FANCA):c.754G>A (p.Asp252Asn) rs111944585
NM_000135.3(FANCA):c.754_755delGAinsAG (p.Asp252Ser) rs587778324
NM_000135.3(FANCA):c.764_766del (p.Arg255del) rs555210441
NM_000135.3(FANCA):c.805G>T (p.Val269Leu) rs1555566973

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