ClinVar Miner

List of variants in gene DOK7 reported as benign by Preventiongenetics, part of Exact Sciences

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Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_173660.5(DOK7):c.332-18T>C rs2699425 0.28202
NM_173660.5(DOK7):c.1382G>A (p.Gly461Asp) rs9684786 0.20663
NM_173660.5(DOK7):c.1185C>T (p.Tyr395=) rs6850908 0.18472
NM_173660.5(DOK7):c.887A>G (p.Gln296Arg) rs6811423 0.18249
NM_173660.5(DOK7):c.1113A>C (p.Ser371=) rs6811856 0.18181
NM_173660.5(DOK7):c.1134G>A (p.Ala378=) rs6831659 0.17563
NM_173660.5(DOK7):c.101-11G>A rs2344209 0.13238
NM_173660.5(DOK7):c.331+27G>A rs77051823 0.09480
NM_173660.5(DOK7):c.1243C>T (p.Pro415Ser) rs16844464 0.06297
NM_173660.5(DOK7):c.331+43G>T rs57204641 0.05537
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.653-19A>C rs191981243 0.01231
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.1204C>T (p.Arg402Trp) rs149905649 0.00516
NM_173660.5(DOK7):c.772+37G>A rs139753457 0.00256
NM_173660.5(DOK7):c.1469C>T (p.Ser490Leu) rs77513082 0.00232
NM_173660.5(DOK7):c.101-26G>A rs2344208
NM_173660.5(DOK7):c.101-26G>C rs2344208
NM_173660.5(DOK7):c.332-49C>T rs114112298
NM_173660.5(DOK7):c.54+29G>T rs767030857
NM_173660.5(DOK7):c.773-32del rs34230391
NM_173660.5(DOK7):c.967C>T (p.Arg323Cys) rs150728781

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