ClinVar Miner

List of variants in gene WDR35 reported as likely benign for not provided

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Gene type:
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Total variants: 46
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HGVS dbSNP gnomAD frequency
NM_020779.4(WDR35):c.2964+243T>G rs144732329 0.01880
NM_020779.4(WDR35):c.736+105G>A rs186022194 0.01354
NM_020779.4(WDR35):c.25-174C>G rs79190097 0.01350
NM_020779.4(WDR35):c.737-104A>C rs146308888 0.01271
NM_020779.4(WDR35):c.1255+237A>G rs116517351 0.01221
NM_020779.4(WDR35):c.1601G>A (p.Arg534Gln) rs113345685 0.01206
NM_020779.4(WDR35):c.2965-29C>T rs145176370 0.01132
NM_020779.4(WDR35):c.1634+176G>A rs77384238 0.01032
NM_020779.4(WDR35):c.2064-140T>G rs75098937 0.00906
NM_020779.4(WDR35):c.882+113C>T rs77041639 0.00868
NM_020779.4(WDR35):c.1926+235A>G rs76264399 0.00829
NM_020779.4(WDR35):c.1401-257C>T rs80076888 0.00553
NM_020779.4(WDR35):c.1471-66C>T rs111873651 0.00489
NM_020779.4(WDR35):c.2659-244C>T rs192737707 0.00427
NM_020779.4(WDR35):c.2824-220A>G rs148535637 0.00407
NM_020779.4(WDR35):c.1195-1507A>G rs74977625 0.00363
NM_020779.4(WDR35):c.2414+20C>T rs116756504 0.00361
NM_020779.4(WDR35):c.1471-173G>C rs111795637 0.00351
NM_020779.4(WDR35):c.215-273C>T rs111821588 0.00351
NM_020779.4(WDR35):c.1471-188A>G rs116018163 0.00335
NM_020779.4(WDR35):c.1195-96T>C rs73216596 0.00319
NM_020779.4(WDR35):c.2262C>T (p.Asp754=) rs147206032 0.00285
NM_020779.4(WDR35):c.318T>C (p.Ile106=) rs115963122 0.00263
NM_020779.4(WDR35):c.1591C>G (p.Leu531Val) rs148242353 0.00233
NM_020779.4(WDR35):c.355C>T (p.Arg119Cys) rs140308808 0.00221
NM_020779.4(WDR35):c.3121+3G>A rs200042577 0.00199
NM_020779.4(WDR35):c.3279G>C (p.Gln1093His) rs148436608 0.00161
NM_020779.4(WDR35):c.1248T>G (p.Ile416Met) rs144701688 0.00145
NM_020779.4(WDR35):c.2965-72T>C rs138803877 0.00143
NM_020779.4(WDR35):c.437-13T>C rs367802842 0.00098
NM_020779.4(WDR35):c.770T>C (p.Val257Ala) rs142955097 0.00095
NM_020779.4(WDR35):c.853A>T (p.Ile285Phe) rs200059077 0.00073
NM_020779.4(WDR35):c.765C>T (p.Tyr255=) rs117255034 0.00013
NM_020779.4(WDR35):c.798C>T (p.Ser266=) rs141118263 0.00004
NM_020779.4(WDR35):c.2361C>T (p.Leu787=) rs768532323 0.00003
NM_020779.4(WDR35):c.1305A>G (p.Lys435=) rs1572344067 0.00001
NM_020779.4(WDR35):c.2267+9T>C rs376307803 0.00001
NM_020779.4(WDR35):c.3122-3T>C rs751769266 0.00001
NM_020779.4(WDR35):c.*6T>G rs189980993
NM_020779.4(WDR35):c.1058G>C (p.Arg353Pro) rs76623454
NM_020779.4(WDR35):c.1401-14_1401-10del
NM_020779.4(WDR35):c.215-222G>A rs148745913
NM_020779.4(WDR35):c.2268-131A>G rs78848859
NM_020779.4(WDR35):c.2659-312_2659-311del rs200283730
NM_020779.4(WDR35):c.3363-72del rs200407223
NM_020779.4(WDR35):c.883-160dup rs61079224

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