List of variants in gene FANCF, LOC130005444 studied for bone marrow disorder

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_022725.4(FANCF):c.883G>A (p.Val295Ile)	rs7103293	0.00448
NM_022725.4(FANCF):c.911G>C (p.Trp304Ser)	rs372140217	0.00009
NM_022725.4(FANCF):c.887G>T (p.Gly296Val)	rs571674814	0.00006
NM_022725.4(FANCF):c.907C>T (p.Pro303Ser)	rs199717587	0.00001
NM_022725.4(FANCF):c.927T>C (p.Asn309=)	rs200073415	0.00001
NM_022725.4(FANCF):c.885T>G (p.Val295=)	rs761238804
NM_022725.4(FANCF):c.886G>T (p.Gly296Ter)
NM_022725.4(FANCF):c.889A>G (p.Thr297Ala)	rs1060501872
NM_022725.4(FANCF):c.891T>G (p.Thr297=)	rs1060504373
NM_022725.4(FANCF):c.898C>T (p.Gln300Ter)
NM_022725.4(FANCF):c.899A>G (p.Gln300Arg)	rs915379462
NM_022725.4(FANCF):c.921G>T (p.Leu307Phe)	rs1205605542
NM_022725.4(FANCF):c.923A>G (p.His308Arg)	rs1590540697
NM_022725.4(FANCF):c.924C>A (p.His308Gln)
NM_022725.4(FANCF):c.924C>T (p.His308=)

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