ClinVar Miner

List of variants in gene ZNF335 studied for autosomal recessive disease

Included ClinVar conditions (1198):
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Gene type:
ClinVar version:
Total variants: 62
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HGVS dbSNP gnomAD frequency
NM_022095.4(ZNF335):c.201+10C>G rs6017715 0.92719
NM_022095.4(ZNF335):c.2021-37C>T rs3746507 0.92505
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.1102+39C>T rs3746513 0.27648
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.1355+13G>A rs3746511 0.09610
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.3487+14G>C rs73622634 0.02516
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.3354C>T (p.Leu1118=) rs35156034 0.01110
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.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.103G>T (p.Val35Leu) rs114356103 0.00300
NM_022095.4(ZNF335):c.3820-11C>T rs191147826 0.00210
NM_022095.4(ZNF335):c.3998A>G (p.Glu1333Gly) rs200635860 0.00025
NM_022095.4(ZNF335):c.808C>T (p.Arg270Cys) rs145110365 0.00022
NM_022095.4(ZNF335):c.1441C>G (p.Arg481Gly) rs141481390 0.00010
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.857G>A (p.Arg286Gln) rs559354455 0.00005
NM_022095.4(ZNF335):c.1505A>G (p.Tyr502Cys) rs753888773 0.00003
NM_022095.4(ZNF335):c.1508G>A (p.Arg503His) rs765260747 0.00003
NM_022095.4(ZNF335):c.1856G>A (p.Arg619His) rs555774487 0.00003
NM_022095.4(ZNF335):c.3868C>T (p.Gln1290Ter) rs770300456 0.00003
NM_022095.4(ZNF335):c.3346G>A (p.Gly1116Arg) rs780393773 0.00001
NM_022095.4(ZNF335):c.1399T>C (p.Cys467Arg) rs1568822376
NM_022095.4(ZNF335):c.1471G>C (p.Asp491His)
NM_022095.4(ZNF335):c.1665+61G>A rs2083829211
NM_022095.4(ZNF335):c.1665G>C (p.Pro555=) rs1201395437
NM_022095.4(ZNF335):c.1748C>T (p.Thr583Met)
NM_022095.4(ZNF335):c.201+85G>A
NM_022095.4(ZNF335):c.2047T>C (p.Cys683Arg)
NM_022095.4(ZNF335):c.2062C>T (p.Arg688Trp)
NM_022095.4(ZNF335):c.2168TCT[1] (p.Phe724del) rs773283542
NM_022095.4(ZNF335):c.235C>T (p.Pro79Ser) rs768996558
NM_022095.4(ZNF335):c.2515_2518dup (p.Thr840fs) rs797046124
NM_022095.4(ZNF335):c.2744_2747del (p.Ser915fs) rs753460205
NM_022095.4(ZNF335):c.2891G>A (p.Cys964Tyr) rs148007831
NM_022095.4(ZNF335):c.3014_3015insG (p.Ser1007fs) rs2145359858
NM_022095.4(ZNF335):c.3158C>T (p.Pro1053Leu) rs768092083
NM_022095.4(ZNF335):c.3206A>G (p.His1069Arg)
NM_022095.4(ZNF335):c.3274C>T (p.Arg1092Trp)
NM_022095.4(ZNF335):c.3332G>A (p.Arg1111His) rs397514642
NM_022095.4(ZNF335):c.3589C>T (p.Gln1197Ter) rs1600517442
NM_022095.4(ZNF335):c.3670-16dup rs201440041
NM_022095.4(ZNF335):c.3787G>T (p.Glu1263Ter) rs749190523
NM_022095.4(ZNF335):c.3820-7_3820-6del rs150750750
NM_022095.4(ZNF335):c.3887_3888del (p.His1296fs)
NM_022095.4(ZNF335):c.715GTG[3] (p.Val242del) rs759141702
NM_022095.4(ZNF335):c.815-3del rs551678383

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