List of variants reported as benign for Fanconi anemia complementation group I by KCCC/NGS Laboratory, Kuwait Cancer Control Center

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Total variants: 27

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HGVS	dbSNP	gnomAD frequency
NM_001113378.2(FANCI):c.288+37G>A	rs16942918	0.47622
NM_001113378.2(FANCI):c.1698+15C>T	rs9806604	0.46880
NM_001113378.2(FANCI):c.3906T>C (p.Gly1302=)	rs1138465	0.41848
NM_001113378.2(FANCI):c.3006+15A>C	rs2159081	0.37877
NM_001113378.2(FANCI):c.545+19C>T	rs1981623	0.37220
NM_001113378.2(FANCI):c.545+30G>A	rs1981624	0.37206
NM_001113378.2(FANCI):c.257C>T (p.Ala86Val)	rs17803620	0.31885
NM_001113378.2(FANCI):c.2225G>C (p.Cys742Ser)	rs2283432	0.29667
NM_001113378.2(FANCI):c.2367G>T (p.Ala789=)	rs11857960	0.07285
NM_001113378.2(FANCI):c.2629A>T (p.Ile877Leu)	rs35875311	0.07245
NM_001113378.2(FANCI):c.164C>T (p.Pro55Leu)	rs62020347	0.04602
NM_001113378.2(FANCI):c.1294-8C>T	rs16942931	0.03299
NM_001113378.2(FANCI):c.2028C>T (p.Ala676=)	rs16942969	0.03295
NM_001113378.2(FANCI):c.3651+19G>A	rs73472624	0.01789
NM_001113378.2(FANCI):c.1114G>A (p.Val372Ile)	rs76788798	0.01679
NM_001113378.2(FANCI):c.868G>A (p.Val290Met)	rs113772230	0.01634
NM_001113378.2(FANCI):c.3846C>T (p.Ser1282=)	rs34557339	0.01219
NM_001113378.2(FANCI):c.1813C>T (p.Leu605Phe)	rs117125761	0.00708
NM_001113378.2(FANCI):c.3525C>A (p.Ala1175=)	rs114810692	0.00625
NM_001113378.2(FANCI):c.1699-7C>A	rs28446881	0.00498
NM_001113378.2(FANCI):c.2056C>A (p.Gln686Lys)	rs28378332	0.00462
NM_001113378.2(FANCI):c.1211T>C (p.Ile404Thr)	rs79080874	0.00400
NM_001113378.2(FANCI):c.2883A>G (p.Gln961=)	rs11556721	0.00322
NM_001113378.2(FANCI):c.1179T>C (p.Tyr393=)	rs3743377	0.00228
NM_001113378.2(FANCI):c.3592-8T>C	rs185599057	0.00200
NM_001113378.2(FANCI):c.2487T>G (p.Leu829=)	rs145762491	0.00155
NM_001113378.2(FANCI):c.286G>A (p.Glu96Lys)	rs149243307	0.00063

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