ClinVar Miner

List of variants in gene CCDC39 reported by Preventiongenetics, part of Exact Sciences

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Gene type:
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Total variants: 29
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HGVS dbSNP gnomAD frequency
NM_181426.2(CCDC39):c.1359C>T (p.Ser453=) rs6769457 0.33560
NM_181426.2(CCDC39):c.1248A>G (p.Glu416=) rs2338436 0.14399
NM_181426.2(CCDC39):c.1528-43A>G rs73051767 0.13950
NM_181426.2(CCDC39):c.472C>G (p.Leu158Val) rs57838737 0.04150
NM_181426.2(CCDC39):c.545C>G (p.Thr182Ser) rs112738198 0.02615
NM_181426.2(CCDC39):c.2230C>G (p.Gln744Glu) rs61733579 0.01895
NM_181426.2(CCDC39):c.604G>A (p.Ala202Thr) rs61733578 0.01102
NM_181426.2(CCDC39):c.2159-16A>C rs147028259 0.00860
NM_181426.2(CCDC39):c.1875-20G>A rs73051759 0.00467
NM_181426.2(CCDC39):c.233G>A (p.Arg78His) rs115952495 0.00435
NM_181426.2(CCDC39):c.930+12C>G rs1401333 0.00338
NM_181426.2(CCDC39):c.1073C>T (p.Thr358Ile) rs183413880 0.00334
NM_181426.2(CCDC39):c.1433A>G (p.Gln478Arg) rs115545935 0.00314
NM_181426.2(CCDC39):c.1008G>A (p.Lys336=) rs79329972 0.00226
NM_181426.2(CCDC39):c.1861C>T (p.Arg621Trp) rs771462228 0.00061
NM_181426.2(CCDC39):c.900T>A (p.His300Gln) rs201684898 0.00057
NM_181426.2(CCDC39):c.1035-5T>C rs200089274 0.00021
NM_181426.2(CCDC39):c.357+8T>C rs374226135 0.00011
NM_181426.2(CCDC39):c.1896A>G (p.Leu632=) rs79353057 0.00010
NM_181426.2(CCDC39):c.1874G>T (p.Ser625Ile) rs769223754 0.00006
NM_181426.2(CCDC39):c.1034+7A>T rs191242640 0.00003
NM_181426.2(CCDC39):c.993T>C (p.Asn331=) rs867488884 0.00002
NM_181426.2(CCDC39):c.1742A>G (p.Glu581Gly) rs768857374 0.00001
NM_181426.2(CCDC39):c.818T>C (p.Ile273Thr) rs201125479 0.00001
NM_181426.2(CCDC39):c.1639C>T (p.Leu547Phe)
NM_181426.2(CCDC39):c.1871_1872del (p.Ile624fs) rs1560086701
NM_181426.2(CCDC39):c.25C>T (p.Leu9=) rs886038750
NM_181426.2(CCDC39):c.853G>A (p.Val285Met) rs886038751
NM_181426.2(CCDC39):c.930+17_930+18del rs765920330

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