List of variants in gene FANCF reported as uncertain significance by Illumina Laboratory Services, Illumina

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: 50

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HGVS	dbSNP	gnomAD frequency
NM_022725.4(FANCF):c.*1879T>C	rs45553340	0.00575
NM_022725.4(FANCF):c.*708C>T	rs61889392	0.00321
NM_022725.4(FANCF):c.*1440A>G	rs191742011	0.00155
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.*1094A>G	rs544116147	0.00031
NM_022725.3(FANCF):c.-31T>C	rs202069513	0.00026
NM_022725.4(FANCF):c.465A>T (p.Pro155=)	rs201215734	0.00020
NM_022725.4(FANCF):c.*2074A>G	rs576419372	0.00013
NM_022725.4(FANCF):c.*1630G>A	rs559054290	0.00012
NM_022725.4(FANCF):c.*1420A>G	rs414664	0.00011
NM_022725.4(FANCF):c.350C>T (p.Pro117Leu)	rs374572943	0.00010
NM_022725.4(FANCF):c.*1512A>G	rs571200561	0.00009
NM_022725.4(FANCF):c.860A>G (p.Tyr287Cys)	rs750623273	0.00009
NM_022725.4(FANCF):c.*336C>A	rs750128615	0.00008
NM_022725.4(FANCF):c.*1535T>A	rs886048151	0.00006
NM_022725.4(FANCF):c.*499T>C	rs566136504	0.00005
NM_022725.4(FANCF):c.*1119T>A	rs558392453	0.00004
NM_022725.4(FANCF):c.*412T>A	rs1310827545	0.00004
NM_022725.3(FANCF):c.-21A>G	rs751857151	0.00003
NM_022725.4(FANCF):c.*1884T>C	rs760103091	0.00003
NM_022725.4(FANCF):c.*2071A>G	rs886048148	0.00003
NM_022725.4(FANCF):c.*597G>A	rs373336301	0.00003
NM_022725.4(FANCF):c.*7C>G	rs770964562	0.00003
NM_022725.4(FANCF):c.101C>T (p.Ala34Val)	rs780228540	0.00003
NM_022725.4(FANCF):c.*555T>C	rs1306529494	0.00002
NM_022725.4(FANCF):c.279C>T (p.Leu93=)	rs199578614	0.00002
NM_022725.4(FANCF):c.*1190C>A	rs750376328	0.00001
NM_022725.4(FANCF):c.*1632G>C	rs886048150	0.00001
NM_022725.4(FANCF):c.*328C>T	rs964106425	0.00001
NM_022725.4(FANCF):c.*565A>G	rs886048155	0.00001
NM_022725.4(FANCF):c.*782A>G	rs949488113	0.00001
NM_022725.4(FANCF):c.210C>T (p.Gly70=)	rs769740744	0.00001
NM_022725.4(FANCF):c.436C>G (p.Leu146Val)	rs779428484	0.00001
NM_022725.4(FANCF):c.680A>G (p.His227Arg)	rs1248152779	0.00001
NM_022725.4(FANCF):c.*1338dup	rs45554234
NM_022725.4(FANCF):c.*1509G>C	rs886048153
NM_022725.4(FANCF):c.*1525T>G	rs886048152
NM_022725.4(FANCF):c.*1696G>A	rs886048149
NM_022725.4(FANCF):c.*286A>G	rs1858607148
NM_022725.4(FANCF):c.*287C>T	rs886048156
NM_022725.4(FANCF):c.*539T>A	rs1858602761
NM_022725.4(FANCF):c.*624G>C	rs768178918
NM_022725.4(FANCF):c.*650ATTAA[1]	rs886048154
NM_022725.4(FANCF):c.*695dup	rs796646840
NM_022725.4(FANCF):c.*857G>A	rs964945469
NM_022725.4(FANCF):c.261_263del (p.His88del)	rs886048158
NM_022725.4(FANCF):c.2T>C (p.Met1Thr)	rs745495865
NM_022725.4(FANCF):c.547G>C (p.Glu183Gln)	rs774728053

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