ClinVar Miner

List of variants in gene WNK1 reported as uncertain significance for not provided

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Gene type:
ClinVar version:
Total variants: 144
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HGVS dbSNP gnomAD frequency
NM_213655.5(WNK1):c.2201C>T (p.Pro734Leu) rs564717613 0.00161
NM_018979.4(WNK1):c.1074C>T (p.Thr358=) rs72648621 0.00160
NM_018979.4(WNK1):c.6150T>C (p.Leu2050=) rs151331381 0.00157
NM_018979.4(WNK1):c.5638G>A (p.Ala1880Thr) rs72650763 0.00097
NM_018979.4(WNK1):c.1855A>G (p.Thr619Ala) rs149388376 0.00086
NM_018979.4(WNK1):c.2459C>G (p.Ser820Cys) rs74056058 0.00074
NM_018979.4(WNK1):c.7021G>A (p.Gly2341Ser) rs146042595 0.00062
NM_213655.5(WNK1):c.2360G>A (p.Arg787Gln) rs550716144 0.00061
NM_018979.4(WNK1):c.578C>A (p.Pro193Gln) rs72647372 0.00058
NM_018979.4(WNK1):c.3578G>A (p.Ser1193Asn) rs72650720 0.00045
NM_018979.4(WNK1):c.2468A>G (p.His823Arg) rs56015776 0.00043
NM_213655.5(WNK1):c.2834G>A (p.Arg945Gln) rs773884230 0.00041
NM_018979.4(WNK1):c.3292A>G (p.Thr1098Ala) rs138216561 0.00026
NM_018979.4(WNK1):c.5720C>T (p.Pro1907Leu) rs200979623 0.00026
NM_213655.5(WNK1):c.2939G>T (p.Ser980Ile) rs372091476 0.00026
NM_213655.5(WNK1):c.3371G>A (p.Gly1124Glu) rs201042606 0.00024
NM_018979.4(WNK1):c.865T>C (p.Ser289Pro) rs200234585 0.00022
NM_018979.4(WNK1):c.5833C>T (p.Arg1945Cys) rs117016551 0.00021
NM_018979.4(WNK1):c.5851A>G (p.Thr1951Ala) rs72650764 0.00020
NM_213655.5(WNK1):c.2143C>T (p.Arg715Cys) rs772257923 0.00017
NM_018979.4(WNK1):c.1834G>A (p.Gly612Ser) rs146450828 0.00014
NM_018979.4(WNK1):c.3188C>T (p.Thr1063Ile) rs201379287 0.00013
NM_213655.5(WNK1):c.2533C>T (p.Arg845Cys) rs200794710 0.00011
NM_213655.5(WNK1):c.2605C>A (p.Leu869Ile) rs377073379 0.00011
NM_018979.4(WNK1):c.5189C>T (p.Thr1730Ile) rs375562377 0.00009
NM_018979.4(WNK1):c.5714T>A (p.Val1905Glu) rs759895083 0.00009
NM_213655.5(WNK1):c.3107C>T (p.Ala1036Val) rs187534119 0.00009
NM_018979.4(WNK1):c.3210T>C (p.Ser1070=) rs72650717 0.00008
NM_213655.5(WNK1):c.2351G>A (p.Arg784His) rs769105175 0.00007
NM_018979.4(WNK1):c.5734A>C (p.Ile1912Leu) rs201995891 0.00006
NM_018979.4(WNK1):c.5870G>A (p.Arg1957His) rs36083875 0.00006
NM_018979.4(WNK1):c.6278G>A (p.Arg2093His) rs200315094 0.00006
NM_213655.5(WNK1):c.2833C>T (p.Arg945Trp) rs185749579 0.00006
NM_018979.4(WNK1):c.3248A>G (p.Asn1083Ser) rs757299559 0.00005
NM_018979.4(WNK1):c.4703A>C (p.His1568Pro) rs776834411 0.00005
NM_213655.5(WNK1):c.2152C>T (p.Arg718Cys) rs786205473 0.00005
NM_018979.4(WNK1):c.1769A>G (p.Lys590Arg) rs780986326 0.00004
NM_018979.4(WNK1):c.187A>C (p.Lys63Gln) rs780699781 0.00004
NM_018979.4(WNK1):c.4247T>C (p.Ile1416Thr) rs763397988 0.00004
NM_018979.4(WNK1):c.4265T>G (p.Val1422Gly) rs779654189 0.00004
NM_018979.4(WNK1):c.5462C>T (p.Ala1821Val) rs371264719 0.00004
NM_213655.5(WNK1):c.2158A>G (p.Met720Val) rs752135045 0.00004
NM_213655.5(WNK1):c.2350C>T (p.Arg784Cys) rs758110645 0.00004
NM_213655.5(WNK1):c.2650G>A (p.Val884Ile) rs764190549 0.00004
NM_213655.5(WNK1):c.2653G>T (p.Val885Phe) rs769092053 0.00004
NM_018979.4(WNK1):c.130G>A (p.Ala44Thr) rs764240024 0.00003
NM_018979.4(WNK1):c.5326G>A (p.Glu1776Lys) rs551435012 0.00003
NM_018979.4(WNK1):c.5546G>A (p.Ser1849Asn) rs766291907 0.00003
NM_213655.5(WNK1):c.2679A>C (p.Arg893Ser) rs1429843547 0.00003
NM_213655.5(WNK1):c.2831C>T (p.Ala944Val) rs780984459 0.00003
NM_213655.5(WNK1):c.2926G>A (p.Gly976Ser) rs369073199 0.00003
NM_018979.4(WNK1):c.2092G>A (p.Val698Ile) rs764336343 0.00002
NM_018979.4(WNK1):c.4826A>G (p.Asn1609Ser) rs775933163 0.00002
NM_018979.4(WNK1):c.5943T>G (p.Phe1981Leu) rs72650765 0.00002
NM_213655.5(WNK1):c.2233G>A (p.Ala745Thr) rs763686798 0.00002
NM_213655.5(WNK1):c.2358C>G (p.His786Gln) rs750430448 0.00002
NM_213655.5(WNK1):c.3070C>T (p.Arg1024Cys) rs760125099 0.00002
NM_018979.4(WNK1):c.1606G>C (p.Val536Leu) rs145646194 0.00001
NM_018979.4(WNK1):c.2677C>G (p.Pro893Ala) rs1206597194 0.00001
NM_018979.4(WNK1):c.3209+3A>G rs886044182 0.00001
NM_018979.4(WNK1):c.3215A>C (p.His1072Pro) rs376433723 0.00001
NM_018979.4(WNK1):c.3314C>G (p.Ser1105Cys) rs767286874 0.00001
NM_018979.4(WNK1):c.341G>T (p.Ser114Ile) rs371331153 0.00001
NM_018979.4(WNK1):c.3545G>A (p.Arg1182Gln) rs749563110 0.00001
NM_018979.4(WNK1):c.459C>G (p.Pro153=) rs1446171264 0.00001
NM_018979.4(WNK1):c.4637C>T (p.Ala1546Val) rs56351358 0.00001
NM_018979.4(WNK1):c.5002T>G (p.Ser1668Ala) rs371813651 0.00001
NM_018979.4(WNK1):c.5258A>G (p.Lys1753Arg) rs752078094 0.00001
NM_018979.4(WNK1):c.5442G>A (p.Ala1814=) rs557930357 0.00001
NM_018979.4(WNK1):c.6101A>G (p.His2034Arg) rs72650766 0.00001
NM_018979.4(WNK1):c.6115A>G (p.Lys2039Glu) rs1359994702 0.00001
NM_018979.4(WNK1):c.6986C>T (p.Pro2329Leu) rs781574573 0.00001
NM_018979.4(WNK1):c.7092del (p.Ser2365fs) rs1565626117 0.00001
NM_213655.5(WNK1):c.2531G>A (p.Arg844Gln) rs765108175 0.00001
NM_213655.5(WNK1):c.3044C>T (p.Ser1015Phe) rs769973198 0.00001
NM_213655.5(WNK1):c.3232C>T (p.Arg1078Trp) rs1383005865 0.00001
NM_213655.5(WNK1):c.3515A>G (p.His1172Arg) rs1064796902 0.00001
NM_213655.5(WNK1):c.3575C>T (p.Thr1192Ile) rs1217942716 0.00001
GRCh37/hg19 12p13.33(chr12:862732-1017641)x1
NM_018979.4(WNK1):c.1088C>T (p.Ser363Leu) rs1555112931
NM_018979.4(WNK1):c.159_161delinsTTG (p.Glu53_Tyr54delinsAspCys) rs1565375322
NM_018979.4(WNK1):c.1829G>T (p.Ser610Ile)
NM_018979.4(WNK1):c.2140-3403dup
NM_018979.4(WNK1):c.2223+8C>A
NM_018979.4(WNK1):c.2264T>C (p.Val755Ala)
NM_018979.4(WNK1):c.2333A>G (p.Gln778Arg) rs72649879
NM_018979.4(WNK1):c.2374-4C>T rs1176268709
NM_018979.4(WNK1):c.2532T>A (p.Ile844=) rs762491690
NM_018979.4(WNK1):c.2685G>C (p.Gln895His) rs2154080557
NM_018979.4(WNK1):c.2692A>T (p.Thr898Ser)
NM_018979.4(WNK1):c.277C>G (p.Leu93Val) rs766628142
NM_018979.4(WNK1):c.2840C>A (p.Pro947Gln)
NM_018979.4(WNK1):c.2891C>A (p.Ser964Tyr)
NM_018979.4(WNK1):c.2896G>A (p.Val966Met) rs886042915
NM_018979.4(WNK1):c.2970C>A (p.Tyr990Ter)
NM_018979.4(WNK1):c.3372+3A>G rs1426580785
NM_018979.4(WNK1):c.3492G>A (p.Val1164=) rs778613425
NM_018979.4(WNK1):c.3530T>G (p.Phe1177Cys) rs1953359993
NM_018979.4(WNK1):c.3770G>A (p.Arg1257Gln)
NM_018979.4(WNK1):c.3991C>A (p.Pro1331Thr) rs200513331
NM_018979.4(WNK1):c.3991C>T (p.Pro1331Ser) rs200513331
NM_018979.4(WNK1):c.410C>T (p.Pro137Leu)
NM_018979.4(WNK1):c.4172G>A (p.Gly1391Asp) rs769373261
NM_018979.4(WNK1):c.4352_4363del (p.Val1451_Ser1454del) rs753602469
NM_018979.4(WNK1):c.4484C>G (p.Thr1495Ser) rs760474824
NM_018979.4(WNK1):c.4504G>A (p.Ala1502Thr) rs2154084293
NM_018979.4(WNK1):c.4529G>A (p.Ser1510Asn)
NM_018979.4(WNK1):c.4578_4582delinsGCGCA (p.His1527_Ser1528delinsArgThr) rs1565583433
NM_018979.4(WNK1):c.469C>A (p.Pro157Thr)
NM_018979.4(WNK1):c.46C>T (p.Leu16=) rs1443431827
NM_018979.4(WNK1):c.4815G>C (p.Gln1605His)
NM_018979.4(WNK1):c.4882C>T (p.Pro1628Ser)
NM_018979.4(WNK1):c.5222C>T (p.Thr1741Ile)
NM_018979.4(WNK1):c.5448+5G>C
NM_018979.4(WNK1):c.5489G>A (p.Gly1830Glu)
NM_018979.4(WNK1):c.5491A>G (p.Thr1831Ala)
NM_018979.4(WNK1):c.5520C>T (p.Val1840=) rs1212431255
NM_018979.4(WNK1):c.571A>T (p.Lys191Ter) rs1565377862
NM_018979.4(WNK1):c.5725C>T (p.Pro1909Ser)
NM_018979.4(WNK1):c.5731G>A (p.Gly1911Ser)
NM_018979.4(WNK1):c.5878G>A (p.Val1960Ile) rs1010227759
NM_018979.4(WNK1):c.6175A>G (p.Met2059Val) rs1298904248
NM_018979.4(WNK1):c.6356C>T (p.Pro2119Leu)
NM_018979.4(WNK1):c.6624C>A (p.Ser2208Arg) rs72650768
NM_018979.4(WNK1):c.6650G>T (p.Ser2217Ile) rs2154103905
NM_018979.4(WNK1):c.6704C>T (p.Pro2235Leu)
NM_018979.4(WNK1):c.6895C>G (p.Leu2299Val) rs143616411
NM_018979.4(WNK1):c.6902G>C (p.Gly2301Ala)
NM_213655.5(WNK1):c.2209C>T (p.Leu737Phe)
NM_213655.5(WNK1):c.2250dup (p.Ser751fs)
NM_213655.5(WNK1):c.2473C>T (p.Arg825Cys) rs1013040631
NM_213655.5(WNK1):c.2722G>C (p.Glu908Gln) rs1592096494
NM_213655.5(WNK1):c.2743G>A (p.Asp915Asn)
NM_213655.5(WNK1):c.2777C>T (p.Ala926Val)
NM_213655.5(WNK1):c.2869T>C (p.Ser957Pro) rs1379384995
NM_213655.5(WNK1):c.2966A>G (p.Gln989Arg) rs879253973
NM_213655.5(WNK1):c.2990A>G (p.Gln997Arg)
NM_213655.5(WNK1):c.3016G>T (p.Gly1006Cys) rs1592098532
NM_213655.5(WNK1):c.3032T>C (p.Leu1011Pro)
NM_213655.5(WNK1):c.3259GAA[1] (p.Glu1088del) rs780566005
NM_213655.5(WNK1):c.3364C>T (p.Pro1122Ser)
NM_213655.5(WNK1):c.3369C>G (p.Ile1123Met)
NM_213655.5(WNK1):c.3451T>C (p.Ser1151Pro) rs759112199
NM_213655.5(WNK1):c.3481C>T (p.Pro1161Ser)

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