ClinVar Miner

List of variants in gene WDR35 reported as uncertain significance for not provided

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Total variants: 68
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HGVS dbSNP gnomAD frequency
NM_020779.4(WDR35):c.1591C>G (p.Leu531Val) rs148242353 0.00233
NM_020779.4(WDR35):c.2066G>A (p.Arg689His) rs74470618 0.00168
NM_020779.4(WDR35):c.1183A>T (p.Asn395Tyr) rs143343508 0.00135
NM_020779.4(WDR35):c.2678T>C (p.Leu893Ser) rs151047156 0.00093
NM_020779.4(WDR35):c.3467T>G (p.Ile1156Arg) rs147325795 0.00072
NM_020779.4(WDR35):c.1227A>G (p.Thr409=) rs148828104 0.00059
NM_020779.4(WDR35):c.1072G>A (p.Val358Ile) rs151227688 0.00051
NM_020779.4(WDR35):c.2936G>A (p.Arg979Gln) rs138076014 0.00047
NM_020779.4(WDR35):c.1051C>G (p.Pro351Ala) rs140753861 0.00045
NM_020779.4(WDR35):c.3026C>G (p.Thr1009Arg) rs201153804 0.00045
NM_020779.4(WDR35):c.2964+10C>A rs201207790 0.00030
NM_001006657.2(WDR35):c.1226C>T (p.Thr409Met) rs143430766 0.00027
NM_020779.4(WDR35):c.2458C>T (p.Arg820Cys) rs141190788 0.00023
NM_020779.4(WDR35):c.2456A>G (p.Glu819Gly) rs139352103 0.00019
NM_001006657.2(WDR35):c.1203C>T (p.Asn401=) rs142103808 0.00017
NM_020779.4(WDR35):c.3252G>A (p.Glu1084=) rs182360785 0.00014
NM_020779.4(WDR35):c.2777A>G (p.Tyr926Cys) rs75602337 0.00013
NM_001006657.2(WDR35):c.1215A>G (p.Thr405=) rs144673252 0.00011
NM_020779.4(WDR35):c.2164C>T (p.Arg722Cys) rs374073530 0.00011
NM_020779.4(WDR35):c.2447G>A (p.Arg816Gln) rs539243373 0.00011
NM_020779.4(WDR35):c.2109T>G (p.Thr703=) rs201822027 0.00008
NM_020779.4(WDR35):c.1376G>A (p.Arg459Gln) rs146380332 0.00006
NM_020779.4(WDR35):c.143-4T>C rs1180620404 0.00004
NM_020779.4(WDR35):c.1637G>A (p.Arg546His) rs529313875 0.00004
NM_020779.4(WDR35):c.3343T>C (p.Leu1115=) rs772304029 0.00004
NM_020779.4(WDR35):c.836A>G (p.Gln279Arg) rs375814330 0.00004
NM_020779.4(WDR35):c.1636C>T (p.Arg546Cys) rs549077153 0.00003
NM_020779.4(WDR35):c.2128C>T (p.Arg710Cys) rs781365658 0.00003
NM_020779.4(WDR35):c.2446C>T (p.Arg816Trp) rs374027943 0.00003
NM_020779.4(WDR35):c.248A>G (p.Tyr83Cys) rs375383465 0.00003
NM_020779.4(WDR35):c.932G>T (p.Trp311Leu) rs200649783 0.00003
NM_020779.4(WDR35):c.1435A>G (p.Met479Val) rs797046099 0.00002
NM_020779.4(WDR35):c.1775A>G (p.Lys592Arg) rs752107469 0.00002
NM_020779.4(WDR35):c.670T>C (p.Cys224Arg) rs757871845 0.00002
NM_001006657.2(WDR35):c.1217T>C (p.Phe406Ser) rs971237623 0.00001
NM_020779.4(WDR35):c.1526G>T (p.Gly509Val) rs398123536 0.00001
NM_020779.4(WDR35):c.1854T>G (p.Ile618Met) rs767714993 0.00001
NM_020779.4(WDR35):c.1871T>G (p.Ile624Ser) rs139252416 0.00001
NM_020779.4(WDR35):c.1930C>G (p.Pro644Ala) rs758919526 0.00001
NM_020779.4(WDR35):c.2524C>T (p.Pro842Ser) rs777217654 0.00001
NM_020779.4(WDR35):c.2885T>G (p.Leu962Arg) rs727504222 0.00001
NM_020779.4(WDR35):c.529A>G (p.Asn177Asp) rs747028453 0.00001
NM_020779.4(WDR35):c.760A>G (p.Met254Val) rs564598017 0.00001
NM_001006657.2(WDR35):c.1208T>C (p.Met403Thr)
NM_020779.4(WDR35):c.1040C>A (p.Ala347Glu) rs1228739567
NM_020779.4(WDR35):c.1283C>G (p.Thr428Ser)
NM_020779.4(WDR35):c.1408C>G (p.His470Asp) rs1558340974
NM_020779.4(WDR35):c.1543A>G (p.Ile515Val)
NM_020779.4(WDR35):c.1901C>A (p.Ser634Tyr)
NM_020779.4(WDR35):c.2024C>T (p.Ala675Val) rs1558332966
NM_020779.4(WDR35):c.2129G>A (p.Arg710His) rs370797645
NM_020779.4(WDR35):c.2149A>C (p.Ile717Leu) rs144493712
NM_020779.4(WDR35):c.2528A>G (p.Glu843Gly) rs2103402440
NM_020779.4(WDR35):c.2663A>G (p.Asn888Ser) rs1670555348
NM_020779.4(WDR35):c.2823G>A (p.Lys941=) rs2103398260
NM_020779.4(WDR35):c.2910C>A (p.Tyr970Ter) rs1558328055
NM_020779.4(WDR35):c.3043G>A (p.Gly1015Arg)
NM_020779.4(WDR35):c.3070C>G (p.Leu1024Val)
NM_020779.4(WDR35):c.3077A>G (p.Gln1026Arg)
NM_020779.4(WDR35):c.329T>G (p.Ile110Ser)
NM_020779.4(WDR35):c.3322A>G (p.Lys1108Glu)
NM_020779.4(WDR35):c.3367G>A (p.Glu1123Lys) rs774573858
NM_020779.4(WDR35):c.3372G>A (p.Gly1124=) rs771077097
NM_020779.4(WDR35):c.437G>C (p.Gly146Ala)
NM_020779.4(WDR35):c.450G>C (p.Trp150Cys) rs886042222
NM_020779.4(WDR35):c.794G>T (p.Gly265Val) rs1572360707
NM_020779.4(WDR35):c.796A>G (p.Ser266Gly)
NM_020779.4(WDR35):c.883-12T>G rs1393592663

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