List of variants reported as uncertain significance for Fanconi anemia complementation group F by Fulgent Genetics, Fulgent Genetics

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Total variants: 43

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HGVS	dbSNP	gnomAD frequency
NM_022725.4(FANCF):c.385C>G (p.Leu129Val)	rs61753271	0.00051
NM_022725.4(FANCF):c.241G>T (p.Ala81Ser)	rs145057187	0.00048
NM_022725.4(FANCF):c.633G>T (p.Gln211His)	rs146975768	0.00045
NM_022725.4(FANCF):c.637C>T (p.Pro213Ser)	rs201382399	0.00039
NM_022725.4(FANCF):c.91G>A (p.Val31Met)	rs11556562	0.00034
NM_022725.4(FANCF):c.573C>G (p.Ser191Arg)	rs146219377	0.00024
NM_022725.4(FANCF):c.647G>C (p.Arg216Pro)	rs192534185	0.00022
NM_022725.4(FANCF):c.452A>T (p.Tyr151Phe)	rs952309844	0.00017
NM_022725.4(FANCF):c.1087C>T (p.Gln363Ter)	rs201285915	0.00010
NM_022725.4(FANCF):c.860A>G (p.Tyr287Cys)	rs750623273	0.00009
NM_022725.4(FANCF):c.617C>T (p.Ala206Val)	rs756213451	0.00007
NM_022725.4(FANCF):c.446A>G (p.Asn149Ser)	rs377309460	0.00004
NM_022725.3(FANCF):c.-21A>G	rs751857151	0.00003
NM_022725.4(FANCF):c.101C>T (p.Ala34Val)	rs780228540	0.00003
NM_022725.4(FANCF):c.149G>C (p.Arg50Pro)	rs371420932	0.00003
NM_022725.4(FANCF):c.302G>C (p.Arg101Pro)	rs1423734778	0.00003
NM_022725.4(FANCF):c.364C>G (p.Arg122Gly)	rs759470099	0.00003
NM_022725.4(FANCF):c.67G>T (p.Val23Phe)	rs777143902	0.00003
NM_022725.4(FANCF):c.58A>G (p.Thr20Ala)	rs1328802237	0.00002
NM_022725.4(FANCF):c.14T>C (p.Leu5Pro)	rs1159900858	0.00001
NM_022725.4(FANCF):c.332T>C (p.Leu111Pro)	rs373385251	0.00001
NM_022725.4(FANCF):c.380A>G (p.Glu127Gly)	rs1216924776	0.00001
NM_022725.4(FANCF):c.583C>A (p.Arg195Ser)	rs1231820160	0.00001
NM_022725.4(FANCF):c.680A>G (p.His227Arg)	rs1248152779	0.00001
NM_022725.4(FANCF):c.705A>C (p.Gln235His)	rs768107677	0.00001
NM_022725.4(FANCF):c.83C>G (p.Pro28Arg)	rs374063561	0.00001
NM_022725.4(FANCF):c.936A>T (p.Gln312His)	rs371631248	0.00001
NM_022725.4(FANCF):c.104T>G (p.Leu35Trp)	rs2133798660
NM_022725.4(FANCF):c.1063C>T (p.Arg355Cys)	rs1858614312
NM_022725.4(FANCF):c.119A>G (p.Tyr40Cys)	rs1359473267
NM_022725.4(FANCF):c.211G>A (p.Gly71Ser)	rs1590542146
NM_022725.4(FANCF):c.318_319delinsCC (p.Ala107Pro)	rs1565055434
NM_022725.4(FANCF):c.370G>T (p.Ala124Ser)	rs201357673
NM_022725.4(FANCF):c.419G>A (p.Arg140Gln)	rs868692458
NM_022725.4(FANCF):c.433A>G (p.Met145Val)	rs766160698
NM_022725.4(FANCF):c.489G>C (p.Met163Ile)	rs1590541541
NM_022725.4(FANCF):c.62C>G (p.Thr21Ser)	rs765672591
NM_022725.4(FANCF):c.688C>T (p.Pro230Ser)	rs773724648
NM_022725.4(FANCF):c.795C>A (p.Ser265Arg)	rs758796858
NM_022725.4(FANCF):c.821A>C (p.Tyr274Ser)	rs144524228
NM_022725.4(FANCF):c.89C>G (p.Thr30Ser)	rs370347668
NM_022725.4(FANCF):c.952C>T (p.Pro318Ser)	rs746120363
NM_022725.4(FANCF):c.992C>T (p.Thr331Ile)	rs1250903119

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