List of variants in gene DOK7 reported as likely benign for not specified

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: 34

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HGVS	dbSNP	gnomAD frequency
NM_173660.5(DOK7):c.-30G>T	rs146168804	0.11265
NM_173660.5(DOK7):c.652+50G>A	rs2006802	0.06939
NM_173660.5(DOK7):c.589G>A (p.Asp197Asn)	rs16844422	0.02362
NM_173660.5(DOK7):c.-6C>G	rs191800156	0.01785
NM_173660.5(DOK7):c.1351C>T (p.Arg451Trp)	rs16844470	0.01433
NM_173660.5(DOK7):c.1317C>T (p.Ser439=)	rs16844467	0.01424
NM_173660.5(DOK7):c.1143C>T (p.Pro381=)	rs56769879	0.01415
NM_173660.5(DOK7):c.782G>A (p.Arg261His)	rs16844460	0.01070
NM_173660.5(DOK7):c.332-4G>A	rs199578351	0.00790
NM_173660.5(DOK7):c.134C>T (p.Ser45Leu)	rs62272670	0.00470
NM_173660.5(DOK7):c.178G>A (p.Glu60Lys)	rs199980106	0.00227
NM_173660.5(DOK7):c.921C>T (p.Ala307=)	rs138148221	0.00170
NM_173660.5(DOK7):c.532+18G>A	rs200487431	0.00153
NM_173660.5(DOK7):c.1008G>A (p.Ser336=)	rs185050737	0.00131
NM_173660.5(DOK7):c.332-43_332-18del	rs781466203	0.00108
NM_173660.5(DOK7):c.331+9C>T	rs370879328	0.00098
NM_173660.5(DOK7):c.296C>T (p.Ala99Val)	rs138010842	0.00046
NM_173660.5(DOK7):c.282C>T (p.His94=)	rs377025553	0.00022
NM_173660.5(DOK7):c.1091G>A (p.Arg364Gln)	rs201304841	0.00019
NM_173660.5(DOK7):c.331+22C>T	rs766725880	0.00014
NM_173660.5(DOK7):c.189C>T (p.Cys63=)	rs372989037	0.00011
NM_173660.5(DOK7):c.1133C>T (p.Ala378Val)	rs371846002	0.00006
NM_173660.5(DOK7):c.822C>T (p.Asp274=)	rs141732576	0.00005
NM_173660.4(DOK7):c.332-121_332-18del104ins234
NM_173660.4(DOK7):c.332-69_332-18del52ins182
NM_173660.5(DOK7):c.*16C>T	rs561308994
NM_173660.5(DOK7):c.100+36del	rs566267525
NM_173660.5(DOK7):c.1470G>C (p.Ser490=)	rs543344505
NM_173660.5(DOK7):c.501C>T (p.Phe167=)	rs1374098055
NM_173660.5(DOK7):c.54+26G>T	rs543525751
NM_173660.5(DOK7):c.55-13C>G	rs886038744
NM_173660.5(DOK7):c.653-19A>G	rs191981243
NM_173660.5(DOK7):c.918C>T (p.Ala306=)	rs141947707
NM_173660.5(DOK7):c.967C>T (p.Arg323Cys)	rs150728781

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