List of variants in gene FANCF reported by Genetic Services Laboratory, University of Chicago

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 30

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HGVS	dbSNP	gnomAD frequency
NM_022725.4(FANCF):c.387C>T (p.Leu129=)	rs45556032	0.00759
NM_022725.4(FANCF):c.557C>T (p.Ala186Val)	rs113910234	0.00595
NM_022725.4(FANCF):c.*1879T>C	rs45553340	0.00575
NM_022725.4(FANCF):c.199A>C (p.Arg67=)	rs146647469	0.00325
NM_022725.4(FANCF):c.246C>T (p.Asn82=)	rs139724351	0.00185
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.573C>G (p.Ser191Arg)	rs146219377	0.00024
NM_022725.4(FANCF):c.647G>C (p.Arg216Pro)	rs192534185	0.00022
NM_022725.4(FANCF):c.687A>T (p.Ser229=)	rs776140806	0.00021
NM_022725.4(FANCF):c.465A>T (p.Pro155=)	rs201215734	0.00020
NM_022725.4(FANCF):c.350C>T (p.Pro117Leu)	rs374572943	0.00010
NM_022725.4(FANCF):c.349C>A (p.Pro117Thr)	rs372625322	0.00008
NM_022725.4(FANCF):c.873A>G (p.Lys291=)	rs757578045	0.00005
NM_022725.4(FANCF):c.785T>C (p.Leu262Ser)	rs368067979	0.00003
NM_022725.4(FANCF):c.279C>T (p.Leu93=)	rs199578614	0.00002
NM_022725.4(FANCF):c.332T>C (p.Leu111Pro)	rs373385251	0.00001
NM_022725.4(FANCF):c.807G>A (p.Ala269=)	rs754312601	0.00001
NM_022725.4(FANCF):c.936A>T (p.Gln312His)	rs371631248	0.00001
NM_022725.4(FANCF):c.301C>T (p.Arg101Trp)	rs760571335
NM_022725.4(FANCF):c.345C>A (p.Leu115=)	rs749884571
NM_022725.4(FANCF):c.412C>A (p.Arg138Ser)	rs565372884
NM_022725.4(FANCF):c.474G>A (p.Gln158=)	rs1858627811
NM_022725.4(FANCF):c.529G>A (p.Val177Met)	rs775816396
NM_022725.4(FANCF):c.555C>T (p.Pro185=)	rs1156693900
NM_022725.4(FANCF):c.618G>C (p.Ala206=)	rs1056134185
NM_022725.4(FANCF):c.632_634dup (p.Gln211dup)	rs748880303
NM_022725.4(FANCF):c.63C>G (p.Thr21=)	rs368275132
NM_022725.4(FANCF):c.774G>A (p.Gly258=)	rs2133796823

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