ClinVar Miner

List of variants in gene DNAJC5 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 31
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HGVS dbSNP gnomAD frequency
NM_025219.3(DNAJC5):c.-12+125G>C rs543059118 0.04621
NM_025219.3(DNAJC5):c.493+22C>T rs75028039 0.03082
NM_025219.3(DNAJC5):c.322-35G>A rs77884883 0.02087
NM_025219.3(DNAJC5):c.321+158_321+159insGCCCG rs1278740369 0.01849
NM_025219.3(DNAJC5):c.*4300C>T rs41278224 0.01781
NM_025219.3(DNAJC5):c.*4117C>T rs11554630 0.01268
NM_025219.3(DNAJC5):c.108-64C>T rs115314888 0.00857
NM_025219.3(DNAJC5):c.321+211A>G rs112959403 0.00852
NM_025219.3(DNAJC5):c.108-61G>A rs116782755 0.00733
NM_025219.3(DNAJC5):c.107+115G>A rs114760990 0.00715
NM_025219.3(DNAJC5):c.321+211_321+212insGTCACTCCTGCCGTGCGGGCG rs1568989668 0.00643
NM_025219.3(DNAJC5):c.321+160_321+203del rs1568989571 0.00551
NM_025219.3(DNAJC5):c.321+210_321+211insGCCCG rs1174161880 0.00525
NM_025219.3(DNAJC5):c.*1364C>T rs61735744 0.00449
NM_025219.3(DNAJC5):c.*1235C>T rs149675982 0.00347
NM_025219.3(DNAJC5):c.*3995A>G rs115323539 0.00344
NM_025219.3(DNAJC5):c.108-62C>T rs181382328 0.00331
NM_025219.3(DNAJC5):c.107+10C>T rs181906972 0.00101
NM_025219.3(DNAJC5):c.282C>T (p.Asn94=) rs113207069 0.00051
NM_025219.3(DNAJC5):c.324C>G (p.Ala108=) rs141103374 0.00013
NM_025219.3(DNAJC5):c.531C>T (p.Ser177=) rs376694698 0.00012
NM_025219.3(DNAJC5):c.237C>T (p.Tyr79=) rs149971662 0.00009
NM_025219.3(DNAJC5):c.108-3C>T rs541118679 0.00004
NM_025219.3(DNAJC5):c.420G>T (p.Ala140=) rs568985915 0.00004
NM_025219.3(DNAJC5):c.444C>T (p.Phe148=) rs772254851 0.00002
NM_025219.3(DNAJC5):c.447C>T (p.Tyr149=) rs780478210 0.00002
NM_025219.3(DNAJC5):c.207C>T (p.Asp69=) rs760881795 0.00001
NM_025219.3(DNAJC5):c.561C>T (p.Asp187=) rs776807695 0.00001
NM_025219.3(DNAJC5):c.*1197_*1249del rs1568991776
NM_025219.3(DNAJC5):c.321+180_321+181insAGGCGCCCGAGTCACTCCTGCCGTGC rs1568989567
NM_025219.3(DNAJC5):c.420G>A (p.Ala140=) rs568985915

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