List of variants in gene GFI1, LOC129930930 studied for leukopenia

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_005263.5(GFI1):c.1198C>T (p.Leu400Phe)	rs143708376	0.00505
NM_005263.5(GFI1):c.1091-5C>T	rs1385981170	0.00006
NM_005263.5(GFI1):c.1188C>T (p.Phe396=)	rs374783582	0.00006
NM_005263.5(GFI1):c.1208A>G (p.Lys403Arg)	rs28936382	0.00004
NM_005263.5(GFI1):c.1119C>T (p.Cys373=)	rs780643435	0.00003
NM_005263.5(GFI1):c.1120G>A (p.Gly374Ser)	rs367740686	0.00001
NM_005263.5(GFI1):c.1091-16C>G
NM_005263.5(GFI1):c.1091-19C>T
NM_005263.5(GFI1):c.1098G>A (p.Lys366=)
NM_005263.5(GFI1):c.1119C>A (p.Cys373Ter)
NM_005263.5(GFI1):c.1126G>A (p.Ala376Thr)
NM_005263.5(GFI1):c.1132A>G (p.Ser378Gly)
NM_005263.5(GFI1):c.1145A>G (p.Asn382Ser)	rs28936381
NM_005263.5(GFI1):c.1162C>T (p.Arg388Cys)
NM_005263.5(GFI1):c.1172C>T (p.Thr391Ile)	rs1359056019
NM_005263.5(GFI1):c.1189G>A (p.Gly397Ser)
NM_005263.5(GFI1):c.1190G>T (p.Gly397Val)
NM_005263.5(GFI1):c.1194C>T (p.Cys398=)	rs1348982767
NM_005263.5(GFI1):c.1209G>A (p.Lys403=)

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