ClinVar Miner

List of variants in gene WDR35 reported as pathogenic

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Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_020779.4(WDR35):c.1690C>T (p.Arg564Ter) rs367810877 0.00024
NM_020779.4(WDR35):c.1889T>G (p.Leu630Ter) rs199952377 0.00019
NM_020779.4(WDR35):c.994C>T (p.Arg332Ter) rs199840434 0.00005
NM_020779.4(WDR35):c.1255+1G>A rs371669862 0.00004
NM_020779.4(WDR35):c.25-2A>G rs397515534 0.00003
NM_020779.4(WDR35):c.3170A>G (p.Tyr1057Cys) rs541910371 0.00003
NM_020779.4(WDR35):c.932G>T (p.Trp311Leu) rs200649783 0.00003
NM_020779.4(WDR35):c.136C>T (p.Gln46Ter) rs767788330 0.00002
NM_020779.4(WDR35):c.1694_1695dup (p.Thr566Ter) rs766096320 0.00002
NM_020779.4(WDR35):c.3345G>A (p.Leu1115=) rs746128772 0.00002
NM_020779.4(WDR35):c.1381C>T (p.Arg461Ter) rs767751856 0.00001
NM_020779.4(WDR35):c.1400+3A>G rs776631281 0.00001
NM_020779.4(WDR35):c.1468del (p.Gln490fs) rs886044119 0.00001
NM_020779.4(WDR35):c.1559T>C (p.Leu520Pro) rs397515533 0.00001
NM_020779.4(WDR35):c.1600C>T (p.Arg534Ter) rs387907085 0.00001
NM_020779.4(WDR35):c.2590G>A (p.Ala864Thr) rs267607175 0.00001
NM_020779.4(WDR35):c.781T>C (p.Trp261Arg) rs431905505 0.00001
NC_000002.11:g.(?_20153575)_(20153759_?)del
NC_000002.11:g.(?_20188906)_(20189063_?)del
NM_001006657.2(WDR35):c.1210dup (p.Glu404fs) rs1327489348
NM_020779.4(WDR35):c.1322G>A (p.Trp441Ter)
NM_020779.4(WDR35):c.143-18T>A rs1553324519
NM_020779.4(WDR35):c.1546C>T (p.Gln516Ter) rs1050086118
NM_020779.4(WDR35):c.1554C>G (p.Tyr518Ter)
NM_020779.4(WDR35):c.1609C>T (p.Gln537Ter)
NM_020779.4(WDR35):c.171_178del (p.Ser59fs)
NM_020779.4(WDR35):c.1844A>G (p.Glu615Gly) rs267607174
NM_020779.4(WDR35):c.1954_1955insAAAC (p.Leu652fs) rs2103406171
NM_020779.4(WDR35):c.206G>A (p.Gly69Asp) rs765513105
NM_020779.4(WDR35):c.2489A>T (p.Asp830Val) rs1553316926
NM_020779.4(WDR35):c.2638dup (p.Thr880fs) rs2103399754
NM_020779.4(WDR35):c.2701G>T (p.Glu901Ter)
NM_020779.4(WDR35):c.2858del (p.Pro953fs) rs397515334
NM_020779.4(WDR35):c.2976del (p.Leu993fs) rs1490771127
NM_020779.4(WDR35):c.297del (p.Met99fs) rs867715686
NM_020779.4(WDR35):c.2998G>T (p.Glu1000Ter) rs886043316
NM_020779.4(WDR35):c.3058C>T (p.His1020Tyr) rs1553316264
NM_020779.4(WDR35):c.307+214_436+1120del
NM_020779.4(WDR35):c.3426G>T (p.Trp1142Cys) rs1553313859
NM_020779.4(WDR35):c.570+1G>C rs2103456695
NM_020779.4(WDR35):c.707G>A (p.Cys236Tyr) rs1672141593

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