ClinVar Miner

Variants in gene ZNF335 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 33
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HGVS dbSNP gnomAD frequency
NM_022095.4(ZNF335):c.201+10C>G rs6017715 0.92719
NM_022095.4(ZNF335):c.881G>C (p.Ser294Thr) rs6032606 0.89832
NM_022095.4(ZNF335):c.642C>T (p.Ser214=) rs3848719 0.32130
NM_022095.4(ZNF335):c.1103-7G>A rs3746512 0.20987
NM_022095.4(ZNF335):c.3522A>T (p.Pro1174=) rs16990951 0.16529
NM_022095.4(ZNF335):c.3384T>C (p.Pro1128=) rs3746503 0.09613
NM_022095.4(ZNF335):c.2595C>A (p.Asp865Glu) rs41280276 0.04003
NM_022095.4(ZNF335):c.2703C>T (p.Ser901=) rs3746504 0.03894
NM_022095.4(ZNF335):c.1623C>T (p.His541=) rs16990964 0.03634
NM_022095.4(ZNF335):c.2253+10G>T rs6130977 0.03629
NM_022095.4(ZNF335):c.3187C>A (p.Arg1063=) rs11905235 0.02405
NM_022095.4(ZNF335):c.2167T>G (p.Phe723Val) rs41305805 0.01624
NM_022095.4(ZNF335):c.1102+9T>C rs112458662 0.01017
NM_022095.4(ZNF335):c.3800C>A (p.Pro1267Gln) rs113958814 0.00829
NM_022095.4(ZNF335):c.3180C>T (p.Pro1060=) rs61729182 0.00669
NM_022095.4(ZNF335):c.3489T>C (p.Thr1163=) rs116077790 0.00661
NM_022095.4(ZNF335):c.1963C>T (p.Pro655Ser) rs117132825 0.00636
NM_022095.4(ZNF335):c.2821G>A (p.Ala941Thr) rs116247914 0.00511
NM_022095.4(ZNF335):c.3507C>T (p.His1169=) rs141812371 0.00420
NM_022095.4(ZNF335):c.826G>A (p.Ala276Thr) rs117802609 0.00417
NM_022095.4(ZNF335):c.2986A>G (p.Thr996Ala) rs146217460 0.00335
NM_022095.4(ZNF335):c.103G>T (p.Val35Leu) rs114356103 0.00300
NM_022095.4(ZNF335):c.3820-11C>T rs191147826 0.00210
NM_022095.4(ZNF335):c.1646+8T>G rs543622714 0.00194
NM_022095.4(ZNF335):c.3392G>A (p.Arg1131Lys) rs114864530 0.00126
NM_022095.4(ZNF335):c.3963C>T (p.Pro1321=) rs114581171 0.00071
NM_022095.4(ZNF335):c.3843A>G (p.Pro1281=) rs35291173 0.00016
NM_022095.4(ZNF335):c.2500C>T (p.Pro834Ser) rs549937846 0.00008
NM_022095.4(ZNF335):c.1830C>G (p.Leu610=) rs60180055 0.00006
NM_022095.4(ZNF335):c.1116G>A (p.Glu372=)
NM_022095.4(ZNF335):c.2572G>A (p.Glu858Lys)
NM_022095.4(ZNF335):c.3670-16dup rs201440041
NM_022095.4(ZNF335):c.3820-7_3820-6del rs150750750

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