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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 99

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HGVS	dbSNP	gnomAD frequency
NM_000135.4(FANCA):c.2574C>G (p.Ser858Arg)	rs17233141	0.00567
NM_000135.4(FANCA):c.1826+12C>T	rs183513839	0.00518
NM_000135.4(FANCA):c.3348+29C>T	rs1800348	0.00360
NM_000135.4(FANCA):c.2216C>T (p.Pro739Leu)	rs45441106	0.00341
NM_000135.4(FANCA):c.1626+16C>T	rs1800333	0.00322
NM_000135.4(FANCA):c.857A>G (p.Gln286Arg)	rs13336566	0.00303
NM_000135.4(FANCA):c.3591G>A (p.Leu1197=)	rs55773634	0.00282
NM_000135.4(FANCA):c.1874G>C (p.Cys625Ser)	rs139235751	0.00230
NM_000135.4(FANCA):c.1830A>G (p.Ala610=)	rs1800338	0.00201
NM_000135.4(FANCA):c.3198T>C (p.Ala1066=)	rs17227071	0.00172
NM_000135.4(FANCA):c.3584G>A (p.Arg1195Gln)	rs138013482	0.00166
NM_000135.4(FANCA):c.1360-10C>G	rs150836356	0.00165
NM_000135.4(FANCA):c.1471-12A>G	rs9282684	0.00163
NM_000135.4(FANCA):c.754G>A (p.Asp252Asn)	rs111944585	0.00158
NM_000135.4(FANCA):c.2977C>A (p.Gln993Lys)	rs140823801	0.00137
NM_000135.4(FANCA):c.2859C>G (p.Asp953Glu)	rs149112292	0.00125
NM_000135.4(FANCA):c.115A>C (p.Arg39=)	rs17232091	0.00116
NM_000135.4(FANCA):c.80-13C>T	rs189841793	0.00110
NM_000135.4(FANCA):c.237C>T (p.Asp79=)	rs144151341	0.00089
NM_000135.4(FANCA):c.3524C>T (p.Pro1175Leu)	rs147017625	0.00083
NM_000135.4(FANCA):c.1626+29C>T	rs1800334	0.00081
NM_000135.4(FANCA):c.2391G>A (p.Ala797=)	rs147882314	0.00076
NM_000135.4(FANCA):c.2364C>T (p.Ala788=)	rs149754397	0.00064
NM_000135.4(FANCA):c.1047G>A (p.Ala349=)	rs144900606	0.00053
NM_000135.4(FANCA):c.3183C>T (p.Ser1061=)	rs1800346	0.00053
NM_000135.4(FANCA):c.3427C>G (p.Leu1143Val)	rs61753269	0.00048
NM_000135.4(FANCA):c.1904C>T (p.Ala635Val)	rs142217479	0.00037
NM_000135.4(FANCA):c.3583C>T (p.Arg1195Trp)	rs143642304	0.00035
NM_000135.4(FANCA):c.543G>A (p.Ala181=)	rs143314367	0.00035
NM_000135.4(FANCA):c.2478G>A (p.Thr826=)	rs147283549	0.00030
NM_000135.4(FANCA):c.801T>C (p.Val267=)	rs55660936	0.00028
NM_000135.4(FANCA):c.2101A>G (p.Lys701Glu)	rs56369086	0.00025
NM_000135.4(FANCA):c.399C>T (p.His133=)	rs56190097	0.00025
NM_000135.4(FANCA):c.2589C>A (p.Gly863=)	rs72807571	0.00024
NM_000135.4(FANCA):c.3723C>T (p.Asn1241=)	rs202107465	0.00021
NM_000135.4(FANCA):c.3348+7G>T	rs185527578	0.00016
NM_000135.4(FANCA):c.3409-9C>G	rs368943794	0.00016
NM_000135.4(FANCA):c.688G>A (p.Val230Ile)	rs144560850	0.00016
NM_000135.4(FANCA):c.1413C>T (p.Val471=)	rs201561753	0.00015
NM_000135.4(FANCA):c.105T>C (p.Tyr35=)	rs747928827	0.00011
NM_000135.4(FANCA):c.2236G>T (p.Ala746Ser)	rs575108446	0.00011
NM_000135.4(FANCA):c.1755C>G (p.Pro585=)	rs144704750	0.00010
NM_000135.4(FANCA):c.634A>C (p.Arg212=)	rs754839730	0.00010
NM_000135.4(FANCA):c.924C>T (p.Gly308=)	rs143255238	0.00010
NM_000135.4(FANCA):c.1567-6C>T	rs377706883	0.00009
NM_000135.4(FANCA):c.1900+7T>A	rs377401016	0.00009
NM_000135.4(FANCA):c.2376T>C (p.Gly792=)	rs756138062	0.00009
NM_000135.4(FANCA):c.2222+7G>A	rs374312736	0.00007
NM_000135.4(FANCA):c.2820A>G (p.Gln940=)	rs776686639	0.00007
NM_000135.4(FANCA):c.2981+4dup	rs75004096	0.00007
NM_000135.4(FANCA):c.3420C>T (p.Asn1140=)	rs369765552	0.00007
NM_000135.4(FANCA):c.918G>A (p.Thr306=)	rs199634699	0.00007
NM_000135.4(FANCA):c.3279C>T (p.Ser1093=)	rs575863400	0.00006
NM_000135.4(FANCA):c.2015-5C>T	rs780349960	0.00005
NM_000135.4(FANCA):c.2317-8C>T	rs753766357	0.00005
NM_000135.4(FANCA):c.1007-6C>T	rs770125368	0.00004
NM_000135.4(FANCA):c.189+7G>A	rs369985388	0.00004
NM_000135.4(FANCA):c.2088C>T (p.Ser696=)	rs150917432	0.00004
NM_000135.4(FANCA):c.3669C>T (p.Asp1223=)	rs187074190	0.00004
NM_000135.4(FANCA):c.3693C>T (p.His1231=)	rs144524132	0.00004
NM_000135.4(FANCA):c.2222+9G>C	rs774316742	0.00003
NM_000135.4(FANCA):c.522+9G>C	rs113051956	0.00003
NM_000135.4(FANCA):c.1007-7C>G	rs111271660	0.00001
NM_000135.4(FANCA):c.1068C>G (p.Thr356=)	rs1161525939	0.00001
NM_000135.4(FANCA):c.1419G>C (p.Leu473=)	rs1337670144	0.00001
NM_000135.4(FANCA):c.1471-8A>G	rs374717514	0.00001
NM_000135.4(FANCA):c.169C>T (p.Leu57=)	rs368828271	0.00001
NM_000135.4(FANCA):c.2010T>C (p.Arg670=)	rs1335322113	0.00001
NM_000135.4(FANCA):c.207T>C (p.Cys69=)	rs941660593	0.00001
NM_000135.4(FANCA):c.2481G>A (p.Arg827=)	rs749895479	0.00001
NM_000135.4(FANCA):c.2487C>T (p.Ser829=)	rs776013293	0.00001
NM_000135.4(FANCA):c.2502G>A (p.Leu834=)	rs770993950	0.00001
NM_000135.4(FANCA):c.2700T>G (p.Ser900=)	rs755783870	0.00001
NM_000135.4(FANCA):c.283+9T>C	rs779593295	0.00001
NM_000135.4(FANCA):c.2994T>C (p.Tyr998=)	rs758384536	0.00001
NM_000135.4(FANCA):c.3612G>A (p.Arg1204=)	rs762402959	0.00001
NM_000135.4(FANCA):c.3626+4C>T	rs772166806	0.00001
NM_000135.4(FANCA):c.675C>T (p.Cys225=)	rs367717307	0.00001
NM_000135.4(FANCA):c.1290G>T (p.Ala430=)	rs1800332
NM_000135.4(FANCA):c.1437A>G (p.Glu479=)	rs2143476678
NM_000135.4(FANCA):c.1471-21C>T
NM_000135.4(FANCA):c.1626+15G>C	rs886038246
NM_000135.4(FANCA):c.1701C>A (p.Thr567=)	rs745466726
NM_000135.4(FANCA):c.1901-8T>A
NM_000135.4(FANCA):c.2133G>A (p.Leu711=)
NM_000135.4(FANCA):c.213A>G (p.Lys71=)
NM_000135.4(FANCA):c.2223-133T>G
NM_000135.4(FANCA):c.2602-19G>C	rs17233225
NM_000135.4(FANCA):c.2859C>T (p.Asp953=)	rs149112292
NM_000135.4(FANCA):c.3165G>A (p.Arg1055=)
NM_000135.4(FANCA):c.3265G>A (p.Val1089Ile)	rs536839082
NM_000135.4(FANCA):c.336C>G (p.Leu112=)	rs774843944
NM_000135.4(FANCA):c.3456C>T (p.Val1152=)
NM_000135.4(FANCA):c.426+10C>T
NM_000135.4(FANCA):c.426+9C>T
NM_000135.4(FANCA):c.826+10T>C	rs536052530
NM_000135.4(FANCA):c.893+83C>A
NM_000135.4(FANCA):c.893+910A>C
NM_000135.4(FANCA):c.893+922G>A

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