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: 45
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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 0.03845
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 0.00812
NM_181426.2(CCDC39):c.1875-20G>A rs73051759 0.00437
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 0.00329
NM_181426.2(CCDC39):c.1433A>G (p.Gln478Arg) rs115545935 0.00312
NM_181426.2(CCDC39):c.1008G>A (p.Lys336=) rs79329972 0.00226
NM_181426.2(CCDC39):c.1363-3del rs551191744 0.00199
NM_181426.2(CCDC39):c.880A>G (p.Arg294Gly) rs61733577 0.00145
NM_181426.2(CCDC39):c.1954C>T (p.Pro652Ser) rs145506099 0.00127
NM_181426.2(CCDC39):c.1865A>G (p.Glu622Gly) rs200277460 0.00114
NM_181426.2(CCDC39):c.1781C>T (p.Thr594Ile) rs140505857 0.00102
NM_181426.2(CCDC39):c.1861C>T (p.Arg621Trp) rs771462228 0.00061
NM_181426.2(CCDC39):c.900T>A (p.His300Gln) rs201684898 0.00054
NM_181426.2(CCDC39):c.162T>C (p.Ser54=) rs201308407 0.00050
NM_181426.2(CCDC39):c.1137T>C (p.Asp379=) rs374132008 0.00035
NM_181426.2(CCDC39):c.1797A>C (p.Arg599=) rs114128856 0.00030
NM_181426.2(CCDC39):c.1035-5T>C rs200089274 0.00024
NM_181426.2(CCDC39):c.1555C>A (p.His519Asn) rs374289303 0.00020
NM_181426.2(CCDC39):c.357+8T>C rs374226135 0.00011
NM_181426.2(CCDC39):c.885G>A (p.Thr295=) rs775454434 0.00011
NM_181426.2(CCDC39):c.1896A>G (p.Leu632=) rs79353057 0.00010
NM_181426.2(CCDC39):c.818T>C (p.Ile273Thr) rs201125479 0.00008
NM_181426.2(CCDC39):c.357+1G>C rs397515392 0.00007
NM_181426.2(CCDC39):c.9C>T (p.Ser3=) rs540762763 0.00007
NM_181426.2(CCDC39):c.1874G>T (p.Ser625Ile) rs769223754 0.00005
NM_181426.2(CCDC39):c.1034+7A>T rs191242640 0.00003
NM_181426.2(CCDC39):c.993T>C (p.Asn331=) rs867488884 0.00003
NM_181426.2(CCDC39):c.1639C>T (p.Leu547Phe) rs912751506 0.00001
NM_181426.2(CCDC39):c.1742A>G (p.Glu581Gly) rs768857374 0.00001
NM_181426.2(CCDC39):c.588T>G (p.Leu196=) rs774527897 0.00001
NM_181426.2(CCDC39):c.1073_1076del (p.Thr358fs) rs878855279
NM_181426.2(CCDC39):c.1167+1258_1167+1270del rs945414657
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.610_613del rs1415346246
NM_181426.2(CCDC39):c.853G>A (p.Val285Met) rs886038751
NM_181426.2(CCDC39):c.930+17_930+18del rs765920330

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