List of variants in gene F5 reported as benign 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 32

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HGVS	dbSNP	gnomAD frequency
NM_000130.5(F5):c.5419+12A>G	rs6009	0.92435
NM_000130.5(F5):c.552G>T (p.Ser184=)	rs6022	0.33707
NM_000130.5(F5):c.3804T>C (p.Ser1268=)	rs1800594	0.33303
NM_000130.5(F5):c.405G>A (p.Ala135=)	rs6029	0.30714
NM_000130.5(F5):c.4095C>T (p.Thr1365=)	rs9332607	0.29522
NM_000130.5(F5):c.5290A>G (p.Met1764Val)	rs6030	0.29437
NM_000130.5(F5):c.2573A>G (p.Lys858Arg)	rs4524	0.24159
NM_000130.5(F5):c.2208C>T (p.Ile736=)	rs6016	0.24147
NM_000130.5(F5):c.2594A>G (p.His865Arg)	rs4525	0.24141
NM_000130.5(F5):c.2301A>G (p.Ser767=)	rs6021	0.24140
NM_000130.5(F5):c.2773A>G (p.Lys925Glu)	rs6032	0.24133
NM_000130.5(F5):c.2235T>C (p.Asn745=)	rs6017	0.23336
NM_000130.5(F5):c.237A>G (p.Gln79=)	rs6028	0.22486
NM_000130.5(F5):c.3948C>T (p.Leu1316=)	rs9287090	0.21875
NM_000130.5(F5):c.3853C>A (p.Leu1285Ile)	rs1046712	0.16155
NM_000130.5(F5):c.319G>C (p.Asp107His)	rs6019	0.14054
NM_000130.5(F5):c.1242A>G (p.Lys414=)	rs6035	0.08632
NM_000130.5(F5):c.1380C>T (p.Asn460=)	rs6015	0.06377
NM_000130.5(F5):c.1716G>A (p.Glu572=)	rs6036	0.06356
NM_000130.5(F5):c.1238T>C (p.Met413Thr)	rs6033	0.06350
NM_000130.5(F5):c.1926C>A (p.Thr642=)	rs6037	0.06314
NM_000130.5(F5):c.730+7C>T	rs6023	0.05754
NM_000130.5(F5):c.2450A>C (p.Asn817Thr)	rs6018	0.05391
NM_000130.5(F5):c.2289A>G (p.Glu763=)	rs6024	0.05387
NM_000130.5(F5):c.6665A>G (p.Asp2222Gly)	rs6027	0.05290
NM_000130.5(F5):c.3980A>G (p.His1327Arg)	rs1800595	0.05074
NM_000130.5(F5):c.6443T>C (p.Met2148Thr)	rs9332701	0.03115
NM_000130.5(F5):c.2425C>T (p.Pro809Ser)	rs6031	0.02430
NM_000130.5(F5):c.816C>T (p.Asn272=)	rs9332578	0.01203
NM_000130.5(F5):c.5054C>G (p.Thr1685Ser)	rs6011	0.00144
NM_000130.5(F5):c.5245C>G (p.Leu1749Val)	rs6034	0.00144
NM_000130.5(F5):c.6194-20C>A	rs6013

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