ClinVar Miner

List of variants in gene ZNF335 reported as benign by GeneDx

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 42
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HGVS dbSNP gnomAD frequency
NM_022095.4(ZNF335):c.2021-37C>T rs3746507 0.92505
NM_022095.4(ZNF335):c.3488-68T>C rs6065910 0.91909
NM_022095.4(ZNF335):c.2443-249G>A rs6073969 0.91506
NM_022095.4(ZNF335):c.881G>C (p.Ser294Thr) rs6032606 0.88895
NM_022095.4(ZNF335):c.2442+189C>T rs3746506 0.63311
NM_022095.4(ZNF335):c.642C>T (p.Ser214=) rs3848719 0.32130
NM_022095.4(ZNF335):c.956-313A>G rs17448680 0.27757
NM_022095.4(ZNF335):c.202-340A>G rs8123864 0.27751
NM_022095.4(ZNF335):c.2020+80del rs59602820 0.27702
NM_022095.4(ZNF335):c.1102+39C>T rs3746513 0.27648
NM_022095.4(ZNF335):c.2021-107C>T rs3746508 0.22247
NM_022095.4(ZNF335):c.1647-321G>T rs6104404 0.21761
NM_022095.4(ZNF335):c.1103-7G>A rs3746512 0.20987
NM_022095.4(ZNF335):c.2021-169A>G rs3746509 0.16784
NM_022095.4(ZNF335):c.3522A>T (p.Pro1174=) rs16990951 0.16743
NM_022095.4(ZNF335):c.2442+202G>A rs3827066 0.11833
NM_022095.4(ZNF335):c.3384T>C (p.Pro1128=) rs3746503 0.10253
NM_022095.4(ZNF335):c.1355+13G>A rs3746511 0.10246
NM_022095.4(ZNF335):c.2702+141T>A rs73128528 0.09741
NM_022095.4(ZNF335):c.956-162G>A rs17448653 0.07178
NM_022095.4(ZNF335):c.2021-74G>C rs41305807 0.05263
NM_022095.4(ZNF335):c.2703-105G>C rs6124760 0.04673
NM_022095.4(ZNF335):c.2703C>T (p.Ser901=) rs3746504 0.04113
NM_022095.4(ZNF335):c.2253+39C>T rs56295229 0.04067
NM_022095.4(ZNF335):c.2595C>A (p.Asp865Glu) rs41280276 0.04003
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.956-182C>T rs74880664 0.03578
NM_022095.4(ZNF335):c.814+46G>A rs76907877 0.03575
NM_022095.4(ZNF335):c.2020+31C>G rs79645412 0.03568
NM_022095.4(ZNF335):c.2021-333T>C rs6130978 0.03505
NM_022095.4(ZNF335):c.2702+324C>G rs73128526 0.03429
NM_022095.4(ZNF335):c.1103-327G>A rs73622638 0.02965
NM_022095.4(ZNF335):c.3487+14G>C rs73622634 0.02822
NM_022095.4(ZNF335):c.3354C>T (p.Leu1118=) rs35156034 0.01110
NM_022095.4(ZNF335):c.826G>A (p.Ala276Thr) rs117802609 0.00417
NM_022095.4(ZNF335):c.*278G>A rs3363
NM_022095.4(ZNF335):c.1534-268C>G rs3893276
NM_022095.4(ZNF335):c.2021-210G>C rs3746510
NM_022095.4(ZNF335):c.2254-140dup rs796983437
NM_022095.4(ZNF335):c.442+131del rs60279086
NM_022095.4(ZNF335):c.815-3del rs551678383

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