List of variants in gene FANCA reported as uncertain significance for not specified

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: 84

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HGVS	dbSNP	gnomAD frequency
NM_000135.4(FANCA):c.1874G>C (p.Cys625Ser)	rs139235751	0.00230
NM_000135.4(FANCA):c.3584G>A (p.Arg1195Gln)	rs138013482	0.00166
NM_000135.4(FANCA):c.2977C>A (p.Gln993Lys)	rs140823801	0.00137
NM_000135.4(FANCA):c.3524C>T (p.Pro1175Leu)	rs147017625	0.00083
NM_000135.4(FANCA):c.3427C>G (p.Leu1143Val)	rs61753269	0.00048
NM_000135.4(FANCA):c.3430C>T (p.Arg1144Trp)	rs143671872	0.00047
NM_000135.4(FANCA):c.3583C>T (p.Arg1195Trp)	rs143642304	0.00035
NM_000135.4(FANCA):c.480G>A (p.Met160Ile)	rs200603300	0.00031
NM_000135.4(FANCA):c.2390C>T (p.Ala797Val)	rs138248569	0.00026
NM_000135.4(FANCA):c.2949T>G (p.Ile983Met)	rs188695241	0.00014
NM_000135.4(FANCA):c.1640C>T (p.Ala547Val)	rs550821697	0.00012
NM_000135.4(FANCA):c.2266C>T (p.Arg756Cys)	rs556748657	0.00012
NM_000135.4(FANCA):c.3157C>T (p.Arg1053Cys)	rs376103033	0.00011
NM_000135.4(FANCA):c.2309G>A (p.Arg770His)	rs145552439	0.00009
NM_000135.4(FANCA):c.2072A>G (p.Asn691Ser)	rs367880372	0.00008
NM_000135.4(FANCA):c.2856G>C (p.Gln952His)	rs200093209	0.00008
NM_000135.4(FANCA):c.3644C>A (p.Ala1215Asp)	rs199601218	0.00008
NM_000135.4(FANCA):c.2222+7G>A	rs374312736	0.00007
NM_000135.4(FANCA):c.1018G>A (p.Val340Ile)	rs774948790	0.00006
NM_000135.4(FANCA):c.2735C>T (p.Thr912Ile)	rs376302719	0.00005
NM_000135.4(FANCA):c.3536C>G (p.Pro1179Arg)	rs141422170	0.00005
NM_000135.4(FANCA):c.1951G>A (p.Gly651Arg)	rs140785340	0.00004
NM_000135.4(FANCA):c.2706C>G (p.Asp902Glu)	rs587778315	0.00004
NM_000135.4(FANCA):c.2982-8C>G	rs781331325	0.00004
NM_000135.4(FANCA):c.3032G>A (p.Arg1011His)	rs200022826	0.00004
NM_000135.4(FANCA):c.793-9T>C	rs757500718	0.00004
NM_000135.4(FANCA):c.1048C>T (p.Arg350Trp)	rs150290184	0.00003
NM_000135.4(FANCA):c.1209G>A (p.Ala403=)	rs773318145	0.00003
NM_000135.4(FANCA):c.1445C>G (p.Pro482Arg)	rs768676657	0.00003
NM_000135.4(FANCA):c.2308C>T (p.Arg770Cys)	rs1354855145	0.00003
NM_000135.4(FANCA):c.3000C>G (p.His1000Gln)	rs750421982	0.00003
NM_000135.4(FANCA):c.301C>G (p.Gln101Glu)	rs140412064	0.00003
NM_000135.4(FANCA):c.3184G>A (p.Gly1062Arg)	rs142379991	0.00003
NM_000135.4(FANCA):c.522+9G>C	rs113051956	0.00003
NM_000135.4(FANCA):c.553C>A (p.Leu185Ile)	rs587778323	0.00003
NM_000135.4(FANCA):c.596+12A>G	rs377151927	0.00003
NM_000135.4(FANCA):c.827-156G>A	rs797045571	0.00003
NM_000135.4(FANCA):c.1558G>C (p.Asp520His)	rs754123446	0.00002
NM_000135.4(FANCA):c.1822A>G (p.Lys608Glu)	rs938278864	0.00002
NM_000135.4(FANCA):c.2967G>A (p.Met989Ile)	rs1178389035	0.00002
NM_000135.4(FANCA):c.2968G>A (p.Asp990Asn)	rs1060501883	0.00002
NM_000135.4(FANCA):c.3181A>G (p.Ser1061Gly)	rs369878171	0.00002
NM_000135.4(FANCA):c.1211A>G (p.Gln404Arg)	rs769664248	0.00001
NM_000135.4(FANCA):c.1808T>C (p.Phe603Ser)	rs766939940	0.00001
NM_000135.4(FANCA):c.1835A>G (p.Lys612Arg)	rs777736014	0.00001
NM_000135.4(FANCA):c.1859C>T (p.Thr620Ile)	rs558276772	0.00001
NM_000135.4(FANCA):c.220C>G (p.Leu74Val)	rs770294560	0.00001
NM_000135.4(FANCA):c.2420C>T (p.Ala807Val)	rs144570744	0.00001
NM_000135.4(FANCA):c.3109C>A (p.Pro1037Thr)	rs771174892	0.00001
NM_000135.4(FANCA):c.3457G>A (p.Asp1153Asn)	rs753036862	0.00001
NM_000135.4(FANCA):c.3550C>T (p.Arg1184Trp)	rs201492940	0.00001
NM_000135.4(FANCA):c.3556A>G (p.Arg1186Gly)	rs748713183	0.00001
NM_000135.4(FANCA):c.3733C>A (p.Gln1245Lys)	rs745665658	0.00001
NM_000135.4(FANCA):c.521A>G (p.Gln174Arg)	rs1378106123	0.00001
NC_000016.9:g.(89818631_89824984)_(89883066_?)dup
NC_000016.9:g.(89877480_89880927)_(89883066_?)dup
NM_000135.4(FANCA):c.1049G>T (p.Arg350Leu)	rs199967286
NM_000135.4(FANCA):c.116G>C (p.Arg39Thr)	rs151089298
NM_000135.4(FANCA):c.1245G>A (p.Met415Ile)	rs1555561439
NM_000135.4(FANCA):c.1247C>T (p.Ala416Val)	rs750689577
NM_000135.4(FANCA):c.1715+8G>A	rs1209332039
NM_000135.4(FANCA):c.1811T>C (p.Ile604Thr)	rs1555551989
NM_000135.4(FANCA):c.1871C>T (p.Ala624Val)	rs146491000
NM_000135.4(FANCA):c.1942G>A (p.Glu648Lys)	rs1427276212
NM_000135.4(FANCA):c.199C>A (p.Pro67Thr)	rs575469396
NM_000135.4(FANCA):c.2070C>T (p.His690=)	rs1422723344
NM_000135.4(FANCA):c.2140C>G (p.Arg714Gly)	rs200284845
NM_000135.4(FANCA):c.2222+6G>A	rs2143339557
NM_000135.4(FANCA):c.2265A>T (p.Gly755=)	rs2143336208
NM_000135.4(FANCA):c.2316+12C>T	rs768355887
NM_000135.4(FANCA):c.2316+9C>T	rs776301232
NM_000135.4(FANCA):c.2601+9A>T	rs771837383
NM_000135.4(FANCA):c.2827G>C (p.Ala943Pro)	rs2143260822
NM_000135.4(FANCA):c.2853-7G>T	rs1244691285
NM_000135.4(FANCA):c.2927A>G (p.Asp976Gly)	rs2143224701
NM_000135.4(FANCA):c.2942G>C (p.Cys981Ser)	rs1555542910
NM_000135.4(FANCA):c.3212G>A (p.Arg1071Lys)	rs924918296
NM_000135.4(FANCA):c.3315C>T (p.Cys1105=)	rs749550737
NM_000135.4(FANCA):c.3540G>A (p.Val1180=)	rs1423399664
NM_000135.4(FANCA):c.3547T>G (p.Cys1183Gly)	rs763856094
NM_000135.4(FANCA):c.377C>G (p.Thr126Arg)	rs139160837
NM_000135.4(FANCA):c.668C>T (p.Ala223Val)	rs749362808
NM_000135.4(FANCA):c.775C>G (p.Pro259Ala)	rs200988394
NM_000135.4(FANCA):c.805G>T (p.Val269Leu)	rs1555566973

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