ClinVar Miner

List of variants in gene ZNF335 reported as likely benign for not specified

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Total variants: 23
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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.3180C>T (p.Pro1060=) rs61729182 0.00669
NM_022095.4(ZNF335):c.2821G>A (p.Ala941Thr) rs116247914 0.00511
NM_022095.4(ZNF335):c.826G>A (p.Ala276Thr) rs117802609 0.00417
NM_022095.4(ZNF335):c.1830C>G (p.Leu610=) rs60180055 0.00006
NM_022095.4(ZNF335):c.2376G>A (p.Thr792=) rs146076876 0.00003
NM_022095.4(ZNF335):c.2611C>T (p.Leu871=) rs369981721 0.00002
NM_022095.4(ZNF335):c.1866G>A (p.Lys622=) rs749165988 0.00001
NM_022095.4(ZNF335):c.3720A>G (p.Glu1240=) rs763575505 0.00001
NM_022095.4(ZNF335):c.3858C>T (p.Val1286=) rs777764325 0.00001
NM_022095.4(ZNF335):c.627A>G (p.Ala209=) rs569696408 0.00001
NM_022095.4(ZNF335):c.3820-7_3820-6del rs150750750

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