ClinVar Miner

List of variants in gene WDR81 reported by CeGaT Center for Human Genetics Tuebingen

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Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_001163809.2(WDR81):c.4843G>A (p.Gly1615Arg) rs143688446 0.00396
NM_001163809.2(WDR81):c.1877C>T (p.Pro626Leu) rs148644987 0.00393
NM_001163809.2(WDR81):c.4737C>T (p.Pro1579=) rs111943038 0.00378
NM_001163809.2(WDR81):c.4324-8G>A rs200150228 0.00260
NM_001163809.2(WDR81):c.3112G>A (p.Gly1038Arg) rs140132367 0.00256
NM_001163809.2(WDR81):c.5231C>T (p.Ala1744Val) rs137952560 0.00203
NM_001163809.2(WDR81):c.3832G>A (p.Gly1278Ser) rs142199236 0.00186
NM_001163809.2(WDR81):c.5161G>A (p.Val1721Ile) rs143022530 0.00163
NM_001163809.2(WDR81):c.5118T>C (p.Leu1706=) rs138211651 0.00139
NM_001163809.2(WDR81):c.3528C>T (p.Thr1176=) rs148375698 0.00129
NM_001163809.2(WDR81):c.3532G>A (p.Ala1178Thr) rs151330612 0.00121
NM_001163809.2(WDR81):c.2254C>T (p.Pro752Ser) rs200781463 0.00113
NM_001163809.2(WDR81):c.2136G>A (p.Gly712=) rs543853235 0.00111
NM_001163809.2(WDR81):c.2871T>C (p.Asn957=) rs369322431 0.00111
NM_001163809.2(WDR81):c.4208G>A (p.Ser1403Asn) rs138488179 0.00068
NM_001163809.2(WDR81):c.4869C>T (p.Tyr1623=) rs147219407 0.00066
NM_001163809.2(WDR81):c.5205G>A (p.Pro1735=) rs148281999 0.00056
NM_001163809.2(WDR81):c.3394G>A (p.Val1132Met) rs199835827 0.00039
NM_001163809.2(WDR81):c.4155G>A (p.Thr1385=) rs143802836 0.00031
NM_001163809.2(WDR81):c.5040C>T (p.Tyr1680=) rs367672346 0.00024
NM_001163809.2(WDR81):c.5582C>T (p.Pro1861Leu) rs151078477 0.00024
NM_001163809.2(WDR81):c.4590C>T (p.Ser1530=) rs377328201 0.00016
NM_001163809.2(WDR81):c.2051A>C (p.Gln684Pro) rs748793270 0.00013
NM_001163809.2(WDR81):c.3154A>G (p.Met1052Val) rs377204514 0.00011
NM_001163809.2(WDR81):c.5106C>T (p.Phe1702=) rs372716005 0.00011
NM_001163809.2(WDR81):c.4315C>T (p.Arg1439Trp) rs141491316 0.00010
NM_001163809.2(WDR81):c.1404C>T (p.Arg468=) rs563017159 0.00009
NM_001163809.2(WDR81):c.5702C>T (p.Ser1901Leu) rs375949504 0.00008
NM_001163809.2(WDR81):c.2424G>A (p.Thr808=) rs576125095 0.00005
NM_001163809.2(WDR81):c.934G>A (p.Asp312Asn) rs757028154 0.00004
NM_001163809.2(WDR81):c.1370G>A (p.Arg457His) rs774987555 0.00003
NM_001163809.2(WDR81):c.1407G>A (p.Ala469=) rs931943166 0.00002
NM_001163809.2(WDR81):c.568C>T (p.Leu190=) rs950737902 0.00002
NM_001163809.2(WDR81):c.1189C>T (p.Arg397Ter) rs1200455844 0.00001
NM_001163809.2(WDR81):c.4266C>T (p.Ser1422=) rs533141873 0.00001
NM_001163809.2(WDR81):c.4842C>T (p.Ser1614=) rs760305001 0.00001
NM_001163809.2(WDR81):c.4921C>T (p.Leu1641=) rs1904616411 0.00001
NM_001163809.2(WDR81):c.5041G>A (p.Gly1681Ser) rs1238396733 0.00001
NM_001163809.2(WDR81):c.2790A>G (p.Ser930=)
NM_001163809.2(WDR81):c.2856A>C (p.Ala952=)
NM_001163809.2(WDR81):c.2989C>T (p.Leu997=)
NM_001163809.2(WDR81):c.3210C>T (p.Gly1070=)
NM_001163809.2(WDR81):c.3585C>T (p.Ala1195=)
NM_001163809.2(WDR81):c.3771T>G (p.Tyr1257Ter) rs1484029774
NM_001163809.2(WDR81):c.4023G>A (p.Gly1341=) rs986609132
NM_001163809.2(WDR81):c.4263G>T (p.Leu1421=)
NM_001163809.2(WDR81):c.4272C>T (p.Pro1424=)
NM_001163809.2(WDR81):c.4576C>G (p.Arg1526Gly) rs145230769
NM_001163809.2(WDR81):c.4782C>G (p.Gly1594=)
NM_001163809.2(WDR81):c.4944G>A (p.Ser1648=)
NM_001163809.2(WDR81):c.4948G>T (p.Ala1650Ser)
NM_001163809.2(WDR81):c.4950C>T (p.Ala1650=)
NM_001163809.2(WDR81):c.4977C>T (p.Ser1659=)
NM_001163809.2(WDR81):c.4995C>T (p.Ser1665=)
NM_001163809.2(WDR81):c.5043C>T (p.Gly1681=)
NM_001163809.2(WDR81):c.5046C>T (p.Asp1682=)
NM_001163809.2(WDR81):c.5074G>A (p.Val1692Ile)
NM_001163809.2(WDR81):c.5148C>T (p.Asp1716=)
NM_001163809.2(WDR81):c.5160C>T (p.His1720=)
NM_001163809.2(WDR81):c.51G>A (p.Gly17=)
NM_001163809.2(WDR81):c.5409C>T (p.Ala1803=)
NM_001163809.2(WDR81):c.5703G>A (p.Ser1901=) rs111744380
NM_001163809.2(WDR81):c.5715G>A (p.Thr1905=)
NM_001163809.2(WDR81):c.681G>A (p.Ser227=)
NM_001163809.2(WDR81):c.792C>A (p.Leu264=)
NM_152348.4(WDR81):c.-131C>T

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