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: 76
Download table as spreadsheet
HGVS dbSNP
NM_001083961.2(WDR62):c.*5G>A rs61740165
NM_001083961.2(WDR62):c.1043+3A>G rs587784541
NM_001083961.2(WDR62):c.1225A>G (p.Asn409Asp) rs146180912
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.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.1480G>A (p.Gly494Arg) rs587784543
NM_001083961.2(WDR62):c.1486C>T (p.Arg496Trp) rs587784544
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.1640C>T (p.Thr547Met) rs756313871
NM_001083961.2(WDR62):c.1641G>A (p.Thr547=) rs2301734
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.1750A>C (p.Thr584Pro) rs76456648
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.193G>A (p.Val65Met) rs387907084
NM_001083961.2(WDR62):c.1941C>A (p.Cys647Ter) rs769688376
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.2271G>A (p.Leu757=) rs61494900
NM_001083961.2(WDR62):c.2490C>T (p.Asn830=) rs587784547
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.2655C>G (p.Tyr885Ter) rs587784549
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.2896G>A (p.Gly966Arg) rs587784550
NM_001083961.2(WDR62):c.2945G>A (p.Ser982Asn) rs11540047
NM_001083961.2(WDR62):c.2972-15G>A rs1014003547
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.3066G>A (p.Ser1022=) rs3746269
NM_001083961.2(WDR62):c.32G>C (p.Arg11Pro) rs587784552
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.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.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.3639C>T (p.Ser1213=) rs45470992
NM_001083961.2(WDR62):c.363del (p.Asp122fs) rs587776901
NM_001083961.2(WDR62):c.3698C>G (p.Ser1233Cys) rs587784560
NM_001083961.2(WDR62):c.3839_3855del (p.Gly1280fs) rs397704725
NM_001083961.2(WDR62):c.3878C>A (p.Ala1293Asp) rs868263026
NM_001083961.2(WDR62):c.3929A>T (p.Gln1310Leu) rs2074435
NM_001083961.2(WDR62):c.3936dup (p.Val1313fs) rs587776900
NM_001083961.2(WDR62):c.3948G>A (p.Gln1316=) rs4375791
NM_001083961.2(WDR62):c.4123G>A (p.Gly1375Ser) rs17851503
NM_001083961.2(WDR62):c.4170A>C (p.Leu1390Phe) rs1008328
NM_001083961.2(WDR62):c.4205_4208del (p.Val1402fs) rs397704721
NM_001083961.2(WDR62):c.4241dup (p.Ser1415fs) rs587776899
NM_001083961.2(WDR62):c.4381T>G (p.Trp1461Gly) rs61734910
NM_001083961.2(WDR62):c.589G>A (p.Val197Ile) rs535488873
NM_001083961.2(WDR62):c.671G>C (p.Trp224Ser) rs267607176
NM_001083961.2(WDR62):c.700-18C>T rs10423651
NM_001083961.2(WDR62):c.75dup (p.Pro26fs) rs1568560516
NM_001083961.2(WDR62):c.82C>G (p.Arg28Gly) rs200283315
NM_001083961.2(WDR62):c.883-4_890del rs1568334868
NM_001083961.2(WDR62):c.964G>C (p.Ala322Pro) rs587784561

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.