ClinVar Miner

List of variants in gene WDR35 reported as uncertain significance by Eurofins NTD LLC (GA)

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Total variants: 22
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HGVS dbSNP gnomAD frequency
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.1051C>G (p.Pro351Ala) rs140753861 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_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.2109T>G (p.Thr703=) rs201822027 0.00008
NM_020779.4(WDR35):c.143-4T>C rs1180620404 0.00004
NM_020779.4(WDR35):c.3343T>C (p.Leu1115=) rs772304029 0.00004
NM_020779.4(WDR35):c.248A>G (p.Tyr83Cys) rs375383465 0.00003
NM_020779.4(WDR35):c.1435A>G (p.Met479Val) rs797046099 0.00002
NM_020779.4(WDR35):c.1526G>T (p.Gly509Val) rs398123536 0.00001
NM_020779.4(WDR35):c.2885T>G (p.Leu962Arg) rs727504222 0.00001
NM_020779.4(WDR35):c.760A>G (p.Met254Val) rs564598017 0.00001
NM_020779.4(WDR35):c.3372G>A (p.Gly1124=) rs771077097
NM_020779.4(WDR35):c.450G>C (p.Trp150Cys) rs886042222

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