ClinVar Miner

List of variants in gene WDR62 studied for Primary autosomal recessive microcephaly 2

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 174
Download table as spreadsheet
HGVS dbSNP
NM_001083961.2(WDR62):c.*45G>A rs769679657
NM_001083961.2(WDR62):c.*45G>C rs769679657
NM_001083961.2(WDR62):c.*57G>A
NM_001083961.2(WDR62):c.*5G>A rs61740165
NM_001083961.2(WDR62):c.1043+3A>G rs587784541
NM_001083961.2(WDR62):c.1064C>T (p.Ala355Val) rs764859949
NM_001083961.2(WDR62):c.1129G>T (p.Val377Leu) rs761204875
NM_001083961.2(WDR62):c.1183G>A (p.Gly395Ser)
NM_001083961.2(WDR62):c.121T>A (p.Cys41Ser)
NM_001083961.2(WDR62):c.1225A>G (p.Asn409Asp) rs146180912
NM_001083961.2(WDR62):c.1233+11C>A
NM_001083961.2(WDR62):c.1233+13C>T rs76130844
NM_001083961.2(WDR62):c.1233+15C>A
NM_001083961.2(WDR62):c.1233+7C>G rs537771936
NM_001083961.2(WDR62):c.1238A>T (p.Tyr413Phe) rs1265156638
NM_001083961.2(WDR62):c.1312C>T (p.Arg438Cys) rs587784542
NM_001083961.2(WDR62):c.1313G>A (p.Arg438His) rs387907082
NM_001083961.2(WDR62):c.1315T>G (p.Phe439Val) rs75230537
NM_001083961.2(WDR62):c.1359C>T (p.Asn453=) rs148667984
NM_001083961.2(WDR62):c.1408C>T (p.Gln470Ter) rs267607177
NM_001083961.2(WDR62):c.142C>T (p.Leu48Phe) rs62109744
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.1480G>A (p.Gly494Arg) rs587784543
NM_001083961.2(WDR62):c.1486C>T (p.Arg496Trp) rs587784544
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.1531G>A (p.Asp511Asn) rs387907083
NM_001083961.2(WDR62):c.1534C>G (p.Arg512Gly) rs201993064
NM_001083961.2(WDR62):c.1576G>A (p.Glu526Lys) rs147875659
NM_001083961.2(WDR62):c.159G>A (p.Glu53=)
NM_001083961.2(WDR62):c.1640C>T (p.Thr547Met) rs756313871
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.1681A>T (p.Ile561Phe) rs587784545
NM_001083961.2(WDR62):c.1684C>G (p.His562Asp) rs1379578836
NM_001083961.2(WDR62):c.1709A>G (p.Tyr570Cys)
NM_001083961.2(WDR62):c.1750A>C (p.Thr584Pro) rs76456648
NM_001083961.2(WDR62):c.180G>A (p.Val60=) rs61742664
NM_001083961.2(WDR62):c.1836+15C>A
NM_001083961.2(WDR62):c.1837-12C>T
NM_001083961.2(WDR62):c.186C>T (p.Leu62=) rs11538454
NM_001083961.2(WDR62):c.189G>T (p.Glu63Asp) rs201053854
NM_001083961.2(WDR62):c.193G>A (p.Val65Met) rs387907084
NM_001083961.2(WDR62):c.1941C>A (p.Cys647Ter) rs769688376
NM_001083961.2(WDR62):c.1977C>T (p.Asn659=) rs79238222
NM_001083961.2(WDR62):c.2000A>G (p.Lys667Arg)
NM_001083961.2(WDR62):c.2007C>T (p.Ser669=) rs765652491
NM_001083961.2(WDR62):c.203T>C (p.Ile68Thr) rs148615988
NM_001083961.2(WDR62):c.2084_2090dup (p.Ser698fs) rs587784546
NM_001083961.2(WDR62):c.2086del (p.Ser696fs) rs863223322
NM_001083961.2(WDR62):c.2211-4G>A rs202109439
NM_001083961.2(WDR62):c.2227C>T (p.His743Tyr) rs142313818
NM_001083961.2(WDR62):c.2237C>T (p.Pro746Leu) rs140864528
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.2334-13T>C
NM_001083961.2(WDR62):c.2334-6C>A rs138928852
NM_001083961.2(WDR62):c.241G>A (p.Gly81Ser)
NM_001083961.2(WDR62):c.2490C>T (p.Asn830=) rs587784547
NM_001083961.2(WDR62):c.2521-13G>C rs79646208
NM_001083961.2(WDR62):c.2529C>T (p.Asp843=) rs144697999
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.2566C>T (p.Arg856Cys) rs370558837
NM_001083961.2(WDR62):c.2584G>A (p.Gly862Ser) rs587784548
NM_001083961.2(WDR62):c.2584G>T (p.Gly862Cys) rs587784548
NM_001083961.2(WDR62):c.2605G>A (p.Gly869Ser) rs377052586
NM_001083961.2(WDR62):c.2624C>T (p.Thr875Ile)
NM_001083961.2(WDR62):c.2655C>G (p.Tyr885Ter) rs587784549
NM_001083961.2(WDR62):c.272G>A (p.Cys91Tyr)
NM_001083961.2(WDR62):c.2742_2743AG[2] (p.Gln918fs) rs764201220
NM_001083961.2(WDR62):c.2782C>T (p.Leu928=) rs12610991
NM_001083961.2(WDR62):c.2787C>T (p.Pro929=) rs886054359
NM_001083961.2(WDR62):c.2788C>T (p.Gln930Ter) rs1599841026
NM_001083961.2(WDR62):c.2814T>C (p.Ser938=)
NM_001083961.2(WDR62):c.2896G>A (p.Gly966Arg) rs587784550
NM_001083961.2(WDR62):c.2945G>A (p.Ser982Asn) rs11540047
NM_001083961.2(WDR62):c.2950A>G (p.Lys984Glu)
NM_001083961.2(WDR62):c.2972-15G>A rs1014003547
NM_001083961.2(WDR62):c.2972A>T (p.Asp991Val) rs749528768
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.2991C>T (p.Ala997=) rs77898819
NM_001083961.2(WDR62):c.3012_3034dup (p.Pro1012fs) rs1555723585
NM_001083961.2(WDR62):c.3033G>A (p.Pro1011=) rs118175551
NM_001083961.2(WDR62):c.3063G>A (p.Thr1021=) rs750350692
NM_001083961.2(WDR62):c.3066G>A (p.Ser1022=) rs3746269
NM_001083961.2(WDR62):c.3161C>G (p.Pro1054Arg) rs777428608
NM_001083961.2(WDR62):c.3220+4G>C rs199678831
NM_001083961.2(WDR62):c.3221-13G>T
NM_001083961.2(WDR62):c.3221-15G>A
NM_001083961.2(WDR62):c.3231C>T (p.Pro1077=) rs187029707
NM_001083961.2(WDR62):c.328G>A (p.Ala110Thr)
NM_001083961.2(WDR62):c.32G>C (p.Arg11Pro) rs587784552
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.332+1G>A rs587784553
NM_001083961.2(WDR62):c.3335+3A>G rs587784554
NM_001083961.2(WDR62):c.3336-5C>G rs587784555
NM_001083961.2(WDR62):c.3348del (p.Phe1117fs) rs797046109
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.3406C>G (p.Arg1136Gly) rs587784556
NM_001083961.2(WDR62):c.3468C>T (p.Leu1156=) rs17851502
NM_001083961.2(WDR62):c.3514+1G>A rs199736219
NM_001083961.2(WDR62):c.3515-7G>A rs368668756
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.3559G>A (p.Val1187Met) rs587784557
NM_001083961.2(WDR62):c.3573C>T (p.Asp1191=) rs1054040
NM_001083961.2(WDR62):c.359C>A (p.Ser120Tyr) rs587784558
NM_001083961.2(WDR62):c.3611G>T (p.Gly1204Val) rs587784559
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.363del (p.Asp122fs) rs587776901
NM_001083961.2(WDR62):c.3674G>A (p.Arg1225His) rs61743589
NM_001083961.2(WDR62):c.3698C>G (p.Ser1233Cys) rs587784560
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.3839_3855del (p.Gly1280fs) rs397704725
NM_001083961.2(WDR62):c.3857G>A (p.Arg1286His)
NM_001083961.2(WDR62):c.3878C>A (p.Ala1293Asp) rs868263026
NM_001083961.2(WDR62):c.391-10C>T rs201568145
NM_001083961.2(WDR62):c.3929A>T (p.Gln1310Leu) rs2074435
NM_001083961.2(WDR62):c.3936dup (p.Val1313fs) rs587776900
NM_001083961.2(WDR62):c.3946C>G (p.Gln1316Glu) rs35811023
NM_001083961.2(WDR62):c.3948G>A (p.Gln1316=) rs4375791
NM_001083961.2(WDR62):c.3950C>T (p.Pro1317Leu)
NM_001083961.2(WDR62):c.4033C>T (p.Arg1345Cys) rs201363122
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.4187G>A (p.Arg1396His) rs372272053
NM_001083961.2(WDR62):c.4205_4208del (p.Val1402fs) rs397704721
NM_001083961.2(WDR62):c.4241dup (p.Ser1415fs) rs587776899
NM_001083961.2(WDR62):c.4266C>T (p.His1422=) rs886054362
NM_001083961.2(WDR62):c.4283T>C (p.Phe1428Ser) rs1599851829
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.4338C>T (p.Thr1446=) rs149289227
NM_001083961.2(WDR62):c.4339G>A (p.Gly1447Arg) rs769860430
NM_001083961.2(WDR62):c.4381T>G (p.Trp1461Gly) rs61734910
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.546C>T (p.Asn182=)
NM_001083961.2(WDR62):c.562-13C>T rs78138007
NM_001083961.2(WDR62):c.570C>T (p.Ile190=) rs374729985
NM_001083961.2(WDR62):c.589G>A (p.Val197Ile) rs535488873
NM_001083961.2(WDR62):c.64A>C (p.Met22Leu)
NM_001083961.2(WDR62):c.669del (p.Trp224fs) rs1599760058
NM_001083961.2(WDR62):c.671G>C (p.Trp224Ser) rs267607176
NM_001083961.2(WDR62):c.699+11G>C rs886054356
NM_001083961.2(WDR62):c.700-18C>T rs10423651
NM_001083961.2(WDR62):c.75dup (p.Pro26fs) rs1568560516
NM_001083961.2(WDR62):c.791G>A (p.Arg264Gln) rs765050364
NM_001083961.2(WDR62):c.803G>C (p.Ser268Thr)
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.824C>T (p.Ser275Leu)
NM_001083961.2(WDR62):c.82C>G (p.Arg28Gly) rs200283315
NM_001083961.2(WDR62):c.836G>A (p.Cys279Tyr)
NM_001083961.2(WDR62):c.866A>G (p.Lys289Arg) rs12327568
NM_001083961.2(WDR62):c.883-4_890del rs1568334868
NM_001083961.2(WDR62):c.892T>C (p.Ser298Pro)
NM_001083961.2(WDR62):c.964G>C (p.Ala322Pro) rs587784561
NM_001083961.2(WDR62):c.984C>T (p.Leu328=)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.