ClinVar Miner

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

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Total variants: 13
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HGVS dbSNP gnomAD frequency
NM_018451.5(CENPJ):c.163C>G (p.Pro55Ala) rs17081389 0.02639
NM_018451.5(CENPJ):c.175A>G (p.Thr59Ala) rs138732534 0.00157
NM_018451.5(CENPJ):c.1960G>A (p.Ala654Thr) rs140927921 0.00121
NM_018451.5(CENPJ):c.2806A>G (p.Ser936Gly) rs75008861 0.00070
NM_018451.5(CENPJ):c.2462C>T (p.Thr821Met) rs144938364 0.00056
NM_018451.5(CENPJ):c.763A>G (p.Thr255Ala) rs150932292 0.00053
NM_018451.5(CENPJ):c.-67+17A>G rs538194617 0.00048
NM_018451.5(CENPJ):c.569-4T>C rs369506056 0.00033
NM_018451.5(CENPJ):c.2852A>G (p.Gln951Arg) rs138675304 0.00021
NM_018451.5(CENPJ):c.1623C>T (p.Pro541=) rs367566036 0.00012
NM_018451.5(CENPJ):c.810A>G (p.Gln270=) rs572213217 0.00001
NM_018451.5(CENPJ):c.1908C>G (p.Arg636=) rs61743613
NM_018451.5(CENPJ):c.2992-17dup rs35599563

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