ClinVar Miner

List of variants in gene WDR62 reported as likely benign for not specified

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Gene type:
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Total variants: 72
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HGVS dbSNP
NM_001083961.2(WDR62):c.*84T>A
NM_001083961.2(WDR62):c.-35A>G rs575160870
NM_001083961.2(WDR62):c.1225A>G (p.Asn409Asp) rs146180912
NM_001083961.2(WDR62):c.1228G>T (p.Val410Leu) rs139460397
NM_001083961.2(WDR62):c.1233+15del rs373693641
NM_001083961.2(WDR62):c.1359C>T (p.Asn453=) rs148667984
NM_001083961.2(WDR62):c.1434C>G (p.Phe478Leu) rs542178534
NM_001083961.2(WDR62):c.1551-16G>A rs562993441
NM_001083961.2(WDR62):c.1575C>T (p.Asp525=) rs192491678
NM_001083961.2(WDR62):c.1641G>T (p.Thr547=) rs2301734
NM_001083961.2(WDR62):c.1643-39G>A rs2301735
NM_001083961.2(WDR62):c.1752C>T (p.Thr584=) rs752866383
NM_001083961.2(WDR62):c.1764C>T (p.Phe588=) rs757137989
NM_001083961.2(WDR62):c.1768+18C>T rs200186710
NM_001083961.2(WDR62):c.1768+28G>A rs77938609
NM_001083961.2(WDR62):c.1842G>A (p.Ser614=) rs752207581
NM_001083961.2(WDR62):c.1959-20A>G rs150830386
NM_001083961.2(WDR62):c.2016C>T (p.Asp672=) rs114968951
NM_001083961.2(WDR62):c.2112G>C (p.Ser704=) rs115453534
NM_001083961.2(WDR62):c.2147-34G>A rs2301736
NM_001083961.2(WDR62):c.2211-4G>A rs202109439
NM_001083961.2(WDR62):c.231C>A (p.Thr77=) rs761921538
NM_001083961.2(WDR62):c.2334-29C>T rs2301737
NM_001083961.2(WDR62):c.2334-6C>A rs138928852
NM_001083961.2(WDR62):c.2343G>A (p.Thr781=) rs769197637
NM_001083961.2(WDR62):c.2529C>T (p.Asp843=) rs144697999
NM_001083961.2(WDR62):c.2666T>C (p.Met889Thr) rs139749569
NM_001083961.2(WDR62):c.269+19C>T rs140267028
NM_001083961.2(WDR62):c.2739+16G>A rs550334968
NM_001083961.2(WDR62):c.2739+19G>A rs755895254
NM_001083961.2(WDR62):c.2766C>T (p.Arg922=) rs373906889
NM_001083961.2(WDR62):c.2975C>T (p.Ser992Leu) rs74518295
NM_001083961.2(WDR62):c.2976G>A (p.Ser992=) rs757294519
NM_001083961.2(WDR62):c.2982G>A (p.Glu994=) rs587784551
NM_001083961.2(WDR62):c.3033G>A (p.Pro1011=) rs118175551
NM_001083961.2(WDR62):c.3087C>T (p.Cys1029=) rs141344823
NM_001083961.2(WDR62):c.3186C>T (p.His1062=) rs373342234
NM_001083961.2(WDR62):c.3271_3273del (p.His1091del) rs794727435
NM_001083961.2(WDR62):c.3303G>A (p.Thr1101=) rs117887683
NM_001083961.2(WDR62):c.3480G>A (p.Lys1160=) rs370515965
NM_001083961.2(WDR62):c.3514+44G>A rs45468494
NM_001083961.2(WDR62):c.3540C>T (p.Ser1180=) rs150100338
NM_001083961.2(WDR62):c.3612C>T (p.Gly1204=) rs139946168
NM_001083961.2(WDR62):c.3621G>A (p.Gln1207=) rs1555724476
NM_001083961.2(WDR62):c.3702C>T (p.Leu1234=) rs143638774
NM_001083961.2(WDR62):c.3762C>G (p.Ser1254=) rs771454761
NM_001083961.2(WDR62):c.3763G>A (p.Val1255Ile) rs146180208
NM_001083961.2(WDR62):c.3786C>T (p.Gly1262=) rs148415080
NM_001083961.2(WDR62):c.3812C>T (p.Ala1271Val) rs111294536
NM_001083961.2(WDR62):c.390+7C>T rs759572399
NM_001083961.2(WDR62):c.3946C>G (p.Gln1316Glu) rs35811023
NM_001083961.2(WDR62):c.3954C>T (p.Gly1318=) rs773442664
NM_001083961.2(WDR62):c.4105C>A (p.Arg1369=) rs201531251
NM_001083961.2(WDR62):c.4153+37C>G rs58041656
NM_001083961.2(WDR62):c.4159C>A (p.Leu1387Ile) rs147652186
NM_001083961.2(WDR62):c.4296C>T (p.Leu1432=) rs765001215
NM_001083961.2(WDR62):c.4311+16G>T rs1309062277
NM_001083961.2(WDR62):c.4312-5T>G rs182467995
NM_001083961.2(WDR62):c.4338C>T (p.Thr1446=) rs149289227
NM_001083961.2(WDR62):c.4501C>T (p.Leu1501=) rs1204833868
NM_001083961.2(WDR62):c.4527G>A (p.Ser1509=) rs374574870
NM_001083961.2(WDR62):c.477G>A (p.Ala159=) rs146485488
NM_001083961.2(WDR62):c.540G>A (p.Val180=) rs1555712171
NM_001083961.2(WDR62):c.561+44C>G rs115806759
NM_001083961.2(WDR62):c.570C>T (p.Ile190=) rs374729985
NM_001083961.2(WDR62):c.693G>A (p.Glu231=) rs145228171
NM_001083961.2(WDR62):c.699+16T>C rs201300686
NM_001083961.2(WDR62):c.700-15C>A rs750692440
NM_001083961.2(WDR62):c.700-18C>T rs10423651
NM_001083961.2(WDR62):c.744C>T (p.Gly248=) rs146898747
NM_001083961.2(WDR62):c.831C>T (p.Leu277=) rs549410799
NM_001083961.2(WDR62):c.866A>G (p.Lys289Arg) rs12327568

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