ClinVar Miner

List of variants in gene CCDC39 reported as likely benign by PreventionGenetics, part of Exact Sciences

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Total variants: 24
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HGVS dbSNP gnomAD frequency
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.1363-3del rs551191744 0.00199
NM_181426.2(CCDC39):c.880A>G (p.Arg294Gly) rs61733577 0.00156
NM_181426.2(CCDC39):c.1781C>T (p.Thr594Ile) rs140505857 0.00109
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.162T>C (p.Ser54=) rs201308407 0.00053
NM_181426.2(CCDC39):c.1137T>C (p.Asp379=) rs374132008 0.00034
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.885G>A (p.Thr295=) rs775454434 0.00011
NM_181426.2(CCDC39):c.1896A>G (p.Leu632=) rs79353057 0.00010
NM_181426.2(CCDC39):c.9C>T (p.Ser3=) rs540762763 0.00007
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.1167+1258_1167+1270del
NM_181426.2(CCDC39):c.1797A>C (p.Arg599=)
NM_181426.2(CCDC39):c.25C>T (p.Leu9=) rs886038750
NM_181426.2(CCDC39):c.588T>G (p.Leu196=)
NM_181426.2(CCDC39):c.853G>A (p.Val285Met) rs886038751
NM_181426.2(CCDC39):c.930+17_930+18del rs765920330

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