ClinVar Miner

List of variants in gene CENPJ reported as benign for not provided

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Total variants: 50
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HGVS dbSNP gnomAD frequency
NM_018451.5(CENPJ):c.444+205G>A rs2290278 0.84836
NM_018451.5(CENPJ):c.3216+7A>G rs9318917 0.80822
NM_018451.5(CENPJ):c.866-244C>T rs2122884 0.52923
NM_018451.5(CENPJ):c.3042A>G (p.Glu1014=) rs3742165 0.47759
NM_018451.5(CENPJ):c.445-80G>A rs2290276 0.33026
NM_018451.5(CENPJ):c.975-283A>G rs1451569 0.32998
NM_018451.5(CENPJ):c.569-168G>A rs3848001 0.32818
NM_018451.5(CENPJ):c.974+278G>A rs10220033 0.18211
NM_018451.5(CENPJ):c.2992-136C>T rs3742166 0.14510
NM_018451.5(CENPJ):c.444+175T>A rs9581200 0.13554
NM_018451.5(CENPJ):c.2693-296A>T rs7323004 0.13527
NM_018451.5(CENPJ):c.974+64A>T rs2122883 0.13526
NM_018451.5(CENPJ):c.445-167G>A rs2290277 0.13504
NM_018451.5(CENPJ):c.2635T>G (p.Ser879Ala) rs17402892 0.10073
NM_018451.5(CENPJ):c.253C>A (p.Pro85Thr) rs9511510 0.10060
NM_018451.5(CENPJ):c.3217-191T>C rs2077356 0.08493
NM_018451.5(CENPJ):c.3216+143C>G rs10450859 0.05912
NM_018451.5(CENPJ):c.1560A>T (p.Thr520=) rs17081368 0.04825
NM_018451.5(CENPJ):c.163C>G (p.Pro55Ala) rs17081389 0.02639
NM_018451.5(CENPJ):c.187G>C (p.Asp63His) rs7336216 0.02151
NM_018451.5(CENPJ):c.1881G>A (p.Pro627=) rs75985315 0.01708
NM_018451.5(CENPJ):c.2825+113_2825+115del rs142067416 0.01647
NM_018451.5(CENPJ):c.2031C>T (p.Ala677=) rs61729909 0.01628
NM_018451.5(CENPJ):c.287A>G (p.His96Arg) rs61739263 0.01206
NM_018451.5(CENPJ):c.1233G>A (p.Pro411=) rs112133852 0.00368
NM_018451.5(CENPJ):c.68A>G (p.Asn23Ser) rs116981543 0.00264
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.2785A>G (p.Lys929Glu) rs141844033 0.00046
NM_018451.5(CENPJ):c.1430C>T (p.Thr477Met) rs193181742 0.00014
NM_018451.5(CENPJ):c.865+12dup rs202014808 0.00004
NM_018451.5(CENPJ):c.776C>T (p.Ala259Val) rs532917061 0.00002
NM_018451.5(CENPJ):c.810A>G (p.Gln270=) rs572213217 0.00001
GRCh37/hg19 13q12.12-12.13(chr13:25472604-25587121)x3
NM_018451.5(CENPJ):c.1908C>G (p.Arg636=) rs61743613
NM_018451.5(CENPJ):c.2991+96_2991+97del rs68159097
NM_018451.5(CENPJ):c.2992-17dup rs35599563
NM_018451.5(CENPJ):c.2992-18_2992-15del rs367835818
NM_018451.5(CENPJ):c.2992-18_2992-16del rs375905817
NM_018451.5(CENPJ):c.2992-18_2992-17del rs151246139
NM_018451.5(CENPJ):c.2992-6del rs35599563
NM_018451.5(CENPJ):c.2992-7_2992-6dup rs35599563
NM_018451.5(CENPJ):c.3216+104dup rs142218247
NM_018451.5(CENPJ):c.3216+1279G>C
NM_018451.5(CENPJ):c.3216+280C>G rs9553462
NM_018451.5(CENPJ):c.3217-191_3217-172del rs71781737
NM_018451.5(CENPJ):c.61A>G (p.Met21Val) rs35498994
NM_018451.5(CENPJ):c.61A>T (p.Met21Leu) rs35498994
NM_018451.5(CENPJ):c.865+253dup rs1352978464

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