ClinVar Miner

List of variants in gene WDR62 studied for Primary Microcephaly 2 With or Without Cortical Malformations

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Total variants: 69
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HGVS dbSNP
NM_001083961.2(WDR62):c.*45G>A rs769679657
NM_001083961.2(WDR62):c.*45G>C rs769679657
NM_001083961.2(WDR62):c.1064C>T (p.Ala355Val) rs764859949
NM_001083961.2(WDR62):c.10G>C (p.Val4Leu) rs147077663
NM_001083961.2(WDR62):c.1233+13C>T rs76130844
NM_001083961.2(WDR62):c.1233+15del rs373693641
NM_001083961.2(WDR62):c.1233+15dup rs373693641
NM_001083961.2(WDR62):c.1359C>T (p.Asn453=) rs148667984
NM_001083961.2(WDR62):c.1470C>T (p.Asp490=) rs45567532
NM_001083961.2(WDR62):c.1479C>T (p.Ala493=) rs150656878
NM_001083961.2(WDR62):c.1489G>A (p.Val497Ile) rs886054358
NM_001083961.2(WDR62):c.1521G>A (p.Leu507=) rs778207666
NM_001083961.2(WDR62):c.1641G>A (p.Thr547=) rs2301734
NM_001083961.2(WDR62):c.1642+8C>T rs143309981
NM_001083961.2(WDR62):c.1642+9G>A rs112789274
NM_001083961.2(WDR62):c.1643-10C>T rs4806263
NM_001083961.2(WDR62):c.180G>A (p.Val60=) rs61742664
NM_001083961.2(WDR62):c.186C>T (p.Leu62=) rs11538454
NM_001083961.2(WDR62):c.1977C>T (p.Asn659=) rs79238222
NM_001083961.2(WDR62):c.2007C>T (p.Ser669=) rs765652491
NM_001083961.2(WDR62):c.2211-4G>A rs202109439
NM_001083961.2(WDR62):c.2227C>T (p.His743Tyr) rs142313818
NM_001083961.2(WDR62):c.2271G>A (p.Leu757=) rs61494900
NM_001083961.2(WDR62):c.2281C>T (p.His761Tyr) rs61744321
NM_001083961.2(WDR62):c.2490C>T (p.Asn830=) rs587784547
NM_001083961.2(WDR62):c.2521-13G>C rs79646208
NM_001083961.2(WDR62):c.253G>A (p.Val85Met) rs146274964
NM_001083961.2(WDR62):c.2549T>C (p.Leu850Ser) rs2285745
NM_001083961.2(WDR62):c.2605G>A (p.Gly869Ser) rs377052586
NM_001083961.2(WDR62):c.269+12del rs797046108
NM_001083961.2(WDR62):c.2787C>T (p.Pro929=) rs886054359
NM_001083961.2(WDR62):c.2972A>T (p.Asp991Val) rs749528768
NM_001083961.2(WDR62):c.3161C>G (p.Pro1054Arg) rs777428608
NM_001083961.2(WDR62):c.3220+4G>C rs199678831
NM_001083961.2(WDR62):c.3231C>T (p.Pro1077=) rs187029707
NM_001083961.2(WDR62):c.3302C>T (p.Thr1101Met) rs147484315
NM_001083961.2(WDR62):c.3303G>A (p.Thr1101=) rs117887683
NM_001083961.2(WDR62):c.3356C>T (p.Pro1119Leu) rs886054360
NM_001083961.2(WDR62):c.3360G>A (p.Arg1120=) rs886054361
NM_001083961.2(WDR62):c.3401T>G (p.Met1134Arg) rs61741470
NM_001083961.2(WDR62):c.3468C>T (p.Leu1156=) rs17851502
NM_001083961.2(WDR62):c.3536C>T (p.Ala1179Val) rs372642550
NM_001083961.2(WDR62):c.3537G>A (p.Ala1179=) rs201341594
NM_001083961.2(WDR62):c.3612C>T (p.Gly1204=) rs139946168
NM_001083961.2(WDR62):c.3639C>T (p.Ser1213=) rs45470992
NM_001083961.2(WDR62):c.3674G>A (p.Arg1225His) rs61743589
NM_001083961.2(WDR62):c.3724G>A (p.Val1242Met) rs143493857
NM_001083961.2(WDR62):c.3810C>T (p.Thr1270=) rs765881142
NM_001083961.2(WDR62):c.3812C>T (p.Ala1271Val) rs111294536
NM_001083961.2(WDR62):c.3929A>T (p.Gln1310Leu) rs2074435
NM_001083961.2(WDR62):c.3946C>G (p.Gln1316Glu) rs35811023
NM_001083961.2(WDR62):c.4123G>A (p.Gly1375Ser) rs17851503
NM_001083961.2(WDR62):c.4144C>T (p.Pro1382Ser) rs772768990
NM_001083961.2(WDR62):c.4159C>A (p.Leu1387Ile) rs147652186
NM_001083961.2(WDR62):c.4170A>C (p.Leu1390Phe) rs1008328
NM_001083961.2(WDR62):c.4266C>T (p.His1422=) rs886054362
NM_001083961.2(WDR62):c.4296C>T (p.Leu1432=) rs765001215
NM_001083961.2(WDR62):c.4312-5T>G rs182467995
NM_001083961.2(WDR62):c.4312T>A (p.Leu1438Met) rs138814793
NM_001083961.2(WDR62):c.4329G>A (p.Gln1443=) rs771131709
NM_001083961.2(WDR62):c.4339G>A (p.Gly1447Arg) rs769860430
NM_001083961.2(WDR62):c.4464G>A (p.Pro1488=) rs754718956
NM_001083961.2(WDR62):c.4546G>A (p.Val1516Met) rs369708392
NM_001083961.2(WDR62):c.562-13C>T rs78138007
NM_001083961.2(WDR62):c.699+11G>C rs886054356
NM_001083961.2(WDR62):c.791G>A (p.Arg264Gln) rs765050364
NM_001083961.2(WDR62):c.820T>G (p.Tyr274Asp) rs746156911
NM_001083961.2(WDR62):c.821A>G (p.Tyr274Cys) rs886054357
NM_001083961.2(WDR62):c.866A>G (p.Lys289Arg) rs12327568

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