ClinVar Miner

List of variants in gene WDR62 reported as uncertain significance by EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

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Total variants: 54
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HGVS dbSNP
NM_001083961.1(WDR62):c.1043+3A>G rs587784541
NM_001083961.1(WDR62):c.1170C>T (p.Asp390=) rs794727965
NM_001083961.1(WDR62):c.1228G>T (p.Val410Leu) rs139460397
NM_001083961.1(WDR62):c.1233+7C>G rs537771936
NM_001083961.1(WDR62):c.1342T>A (p.Ser448Thr) rs144072948
NM_001083961.1(WDR62):c.1371+6T>G rs1555716725
NM_001083961.1(WDR62):c.156C>G (p.Ser52=) rs398123559
NM_001083961.1(WDR62):c.1576G>A (p.Glu526Lys) rs147875659
NM_001083961.1(WDR62):c.1769-7C>T rs137919897
NM_001083961.1(WDR62):c.1873G>A (p.Val625Ile) rs756425549
NM_001083961.1(WDR62):c.189G>T (p.Glu63Asp) rs201053854
NM_001083961.1(WDR62):c.1927G>A (p.Val643Met) rs759534168
NM_001083961.1(WDR62):c.1959-10A>C rs767989054
NM_001083961.1(WDR62):c.1977C>T (p.Asn659=) rs79238222
NM_001083961.1(WDR62):c.203T>C (p.Ile68Thr) rs148615988
NM_001083961.1(WDR62):c.2040T>C (p.His680=) rs765451882
NM_001083961.1(WDR62):c.2211-4G>A rs202109439
NM_001083961.1(WDR62):c.2227C>T (p.His743Tyr) rs142313818
NM_001083961.1(WDR62):c.2237C>T (p.Pro746Leu) rs140864528
NM_001083961.1(WDR62):c.2381C>G (p.Pro794Arg) rs149431376
NM_001083961.1(WDR62):c.2527G>T (p.Asp843Tyr) rs370738148
NM_001083961.1(WDR62):c.2580C>T (p.Pro860=) rs886043531
NM_001083961.1(WDR62):c.2610A>G (p.Gln870=) rs886043560
NM_001083961.1(WDR62):c.2766C>T (p.Arg922=) rs373906889
NM_001083961.1(WDR62):c.2887G>A (p.Val963Met) rs113046428
NM_001083961.1(WDR62):c.28G>T (p.Ala10Ser) rs774912957
NM_001083961.1(WDR62):c.2976G>A (p.Ser992=) rs757294519
NM_001083961.1(WDR62):c.3087C>T (p.Cys1029=) rs141344823
NM_001083961.1(WDR62):c.3162G>A (p.Pro1054=) rs200232641
NM_001083961.1(WDR62):c.3232G>A (p.Ala1078Thr) rs373781801
NM_001083961.1(WDR62):c.3302C>T (p.Thr1101Met) rs147484315
NM_001083961.1(WDR62):c.3303G>A (p.Thr1101=) rs117887683
NM_001083961.1(WDR62):c.3440A>G (p.Tyr1147Cys) rs146867414
NM_001083961.1(WDR62):c.3612C>T (p.Gly1204=) rs139946168
NM_001083961.1(WDR62):c.3748C>G (p.Arg1250Gly) rs755558753
NM_001083961.1(WDR62):c.37G>C (p.Asp13His) rs886044286
NM_001083961.1(WDR62):c.4122C>T (p.Gly1374=) rs773948810
NM_001083961.1(WDR62):c.4159C>A (p.Leu1387Ile) rs147652186
NM_001083961.1(WDR62):c.4403C>T (p.Ala1468Val) rs148312358
NM_001083961.1(WDR62):c.4441G>A (p.Ala1481Thr) rs761614407
NM_001083961.1(WDR62):c.4481A>G (p.Tyr1494Cys) rs886043267
NM_001083961.1(WDR62):c.4549C>T (p.Arg1517Trp) rs373621531
NM_001083961.1(WDR62):c.477G>A (p.Ala159=) rs146485488
NM_001083961.1(WDR62):c.525C>T (p.Tyr175=) rs779093591
NM_001083961.1(WDR62):c.820T>G (p.Tyr274Asp) rs746156911
NM_001083961.1(WDR62):c.82C>T (p.Arg28Trp) rs200283315
NM_001083961.1(WDR62):c.922A>G (p.Ile308Val) rs146229976
NM_001083961.2(WDR62):c.1990_1992del (p.Lys664del)
NM_001083961.2(WDR62):c.2318G>A (p.Arg773Gln)
NM_001083961.2(WDR62):c.3058G>A (p.Ala1020Thr)
NM_001083961.2(WDR62):c.3221A>G (p.Glu1074Gly)
NM_001083961.2(WDR62):c.3294T>C (p.Ser1098=)
NM_001083961.2(WDR62):c.3596C>G (p.Ser1199Cys)
NM_001083961.2(WDR62):c.3641C>T (p.Thr1214Ile)

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