ClinVar Miner

List of variants in gene ZNF335 studied for not specified

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Total variants: 55
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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.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.3488-6G>A rs201983124 0.00338
NM_022095.4(ZNF335):c.1646+5G>T rs149232277 0.00083
NM_022095.4(ZNF335):c.3445A>G (p.Ile1149Val) rs143113106 0.00075
NM_022095.4(ZNF335):c.2185A>T (p.Ile729Phe) rs190178539 0.00039
NM_022095.4(ZNF335):c.1217T>G (p.Val406Gly) rs141949131 0.00036
NM_022095.4(ZNF335):c.293G>A (p.Gly98Glu) rs34015709 0.00028
NM_022095.4(ZNF335):c.808C>T (p.Arg270Cys) rs145110365 0.00022
NM_022095.4(ZNF335):c.2961G>A (p.Gln987=) rs181061162 0.00017
NM_022095.4(ZNF335):c.-10C>T rs199929676 0.00016
NM_022095.4(ZNF335):c.3639C>T (p.Thr1213=) rs191074858 0.00016
NM_022095.4(ZNF335):c.3843A>G (p.Pro1281=) rs35291173 0.00016
NM_022095.4(ZNF335):c.648G>A (p.Pro216=) rs201180565 0.00013
NM_022095.4(ZNF335):c.4006G>A (p.Val1336Ile) rs372687838 0.00011
NM_022095.4(ZNF335):c.871T>G (p.Ser291Ala) rs371249915 0.00011
NM_022095.4(ZNF335):c.1664C>T (p.Pro555Leu) rs756223963 0.00010
NM_022095.4(ZNF335):c.1830C>G (p.Leu610=) rs60180055 0.00006
NM_022095.4(ZNF335):c.3415C>T (p.Arg1139Trp) rs200221426 0.00006
NM_022095.4(ZNF335):c.2063G>A (p.Arg688Gln) rs760410435 0.00004
NM_022095.4(ZNF335):c.2253+3A>G rs200995811 0.00004
NM_022095.4(ZNF335):c.3444C>T (p.Thr1148=) rs759216909 0.00004
NM_022095.4(ZNF335):c.593A>G (p.Asp198Gly) rs770813545 0.00004
NM_022095.4(ZNF335):c.2376G>A (p.Thr792=) rs146076876 0.00003
NM_022095.4(ZNF335):c.3068T>C (p.Ile1023Thr) rs544636355 0.00003
NM_022095.4(ZNF335):c.3670-8A>C rs772015167 0.00003
NM_022095.4(ZNF335):c.2460G>A (p.Ser820=) rs774396968 0.00002
NM_022095.4(ZNF335):c.2611C>T (p.Leu871=) rs369981721 0.00002
NM_022095.4(ZNF335):c.2653A>G (p.Thr885Ala) rs200004418 0.00002
NM_022095.4(ZNF335):c.1405A>G (p.Ile469Val) rs142224018 0.00001
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.147_152dup (p.Glu50_Ala51dup) rs1555852178
NM_022095.4(ZNF335):c.2168TCT[1] (p.Phe724del) rs773283542
NM_022095.4(ZNF335):c.2564C>T (p.Ala855Val) rs564168844
NM_022095.4(ZNF335):c.3820-7_3820-6del rs150750750
NM_022095.4(ZNF335):c.815-3del rs551678383
NM_022095.4(ZNF335):c.825C>T (p.Ala275=) rs797046125

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