List of variants in gene F9 reported by PreventionGenetics, part of Exact Sciences

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_000133.4(F9):c.580A>G (p.Thr194Ala)	rs6048	0.22614
NM_000133.4(F9):c.1110G>A (p.Gln370=)	rs34698779	0.00833
NM_000133.4(F9):c.967G>A (p.Glu323Lys)	rs150351950	0.00294
NM_000133.4(F9):c.696T>C (p.Asp232=)	rs140835723	0.00113
NM_000133.4(F9):c.819T>C (p.Val273=)	rs1800455	0.00110
NM_000133.4(F9):c.1257G>T (p.Val419=)	rs61731481	0.00100
NM_000133.4(F9):c.19A>T (p.Ile7Phe)	rs150190385	0.00086
NM_000133.4(F9):c.907C>T (p.His303Tyr)	rs1801202	0.00044
NM_000133.4(F9):c.8G>A (p.Arg3His)	rs148060786	0.00042
NM_000133.4(F9):c.1029C>T (p.Asn343=)	rs145026483	0.00017
NM_000133.4(F9):c.769G>A (p.Val257Ile)	rs200608775	0.00010
NM_000133.4(F9):c.316G>A (p.Gly106Ser)	rs137852233	0.00004
NM_000133.4(F9):c.658T>A (p.Ser220Thr)	rs777361659	0.00004
NM_000133.4(F9):c.1150C>T (p.Arg384Ter)	rs137852261	0.00001
NM_000133.4(F9):c.*828GT[6]	rs35599944
NM_000133.4(F9):c.1032C>T (p.Ile344=)	rs886038243
NM_000133.4(F9):c.1168A>T (p.Ile390Phe)
NM_000133.4(F9):c.1293G>A (p.Trp431Ter)
NM_000133.4(F9):c.277+1G>T
NM_000133.4(F9):c.457G>A (p.Val153Met)
NM_000133.4(F9):c.464G>C (p.Cys155Ser)
NM_000133.4(F9):c.595G>A (p.Val199Met)
NM_000133.4(F9):c.676C>T (p.Arg226Trp)	rs137852240
NM_000133.4(F9):c.706_707delinsCT (p.Gly236Leu)
NM_000133.4(F9):c.839-20dup	rs773613916
NM_000133.4(F9):c.858G>T (p.Glu286Asp)

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