ClinVar Miner

List of variants in gene WNK4 reported as uncertain significance for not provided

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Gene type:
ClinVar version:
Total variants: 110
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HGVS dbSNP gnomAD frequency
NM_032387.5(WNK4):c.1885C>T (p.Arg629Cys) rs61755600 0.00123
NM_032387.5(WNK4):c.2476G>A (p.Gly826Ser) rs190384194 0.00070
NM_032387.5(WNK4):c.1800del (p.Ala601fs) rs61755595 0.00028
NM_032387.5(WNK4):c.3553C>T (p.Arg1185Cys) rs137853095 0.00024
NM_032387.5(WNK4):c.1323A>T (p.Glu441Asp) rs387907562 0.00006
NM_032387.5(WNK4):c.1222A>T (p.Ile408Phe) rs369420670 0.00001
NM_032387.5(WNK4):c.1444C>T (p.Arg482Trp) rs387907556 0.00001
NM_032387.5(WNK4):c.14C>T (p.Pro5Leu) rs577125376 0.00001
NM_032387.5(WNK4):c.2084C>G (p.Thr695Ser) rs387907561 0.00001
NM_032387.5(WNK4):c.3536C>T (p.Ala1179Val) rs387907560 0.00001
NM_032387.5(WNK4):c.643C>T (p.Arg215Trp) rs758123242 0.00001
NM_032387.5(WNK4):c.1241G>C (p.Arg414Pro)
NM_032387.5(WNK4):c.1246G>T (p.Asp416Tyr)
NM_032387.5(WNK4):c.1294T>C (p.Phe432Leu)
NM_032387.5(WNK4):c.1306C>A (p.Arg436Ser)
NM_032387.5(WNK4):c.1310G>A (p.Gly437Asp)
NM_032387.5(WNK4):c.133C>A (p.Arg45Ser)
NM_032387.5(WNK4):c.1342G>T (p.Gly448Cys)
NM_032387.5(WNK4):c.1352C>T (p.Pro451Leu)
NM_032387.5(WNK4):c.1398dup (p.Arg467fs)
NM_032387.5(WNK4):c.144del (p.Lys49fs)
NM_032387.5(WNK4):c.1456G>A (p.Glu486Lys)
NM_032387.5(WNK4):c.1477-12C>G
NM_032387.5(WNK4):c.1481C>G (p.Ala494Gly)
NM_032387.5(WNK4):c.148G>A (p.Ala50Thr)
NM_032387.5(WNK4):c.1510C>T (p.Gln504Ter) rs200593980
NM_032387.5(WNK4):c.1555C>T (p.Arg519Ter)
NM_032387.5(WNK4):c.1562G>A (p.Arg521His)
NM_032387.5(WNK4):c.1564G>T (p.Glu522Ter)
NM_032387.5(WNK4):c.157C>G (p.Arg53Gly)
NM_032387.5(WNK4):c.1666C>G (p.Pro556Ala)
NM_032387.5(WNK4):c.1694A>C (p.Gln565Pro)
NM_032387.5(WNK4):c.1742-1G>A rs753483211
NM_032387.5(WNK4):c.1742-5A>G
NM_032387.5(WNK4):c.1822G>T (p.Val608Leu)
NM_032387.5(WNK4):c.1822del (p.Val608fs) rs762079039
NM_032387.5(WNK4):c.1822dup (p.Val608fs)
NM_032387.5(WNK4):c.1862C>T (p.Ser621Leu)
NM_032387.5(WNK4):c.1892G>A (p.Gly631Asp) rs387907557
NM_032387.5(WNK4):c.1912C>T (p.Pro638Ser)
NM_032387.5(WNK4):c.1913C>G (p.Pro638Arg)
NM_032387.5(WNK4):c.1967G>A (p.Gly656Glu)
NM_032387.5(WNK4):c.2014C>T (p.Pro672Ser)
NM_032387.5(WNK4):c.2017C>T (p.Arg673Ter) rs749704694
NM_032387.5(WNK4):c.2041-7_2041-2del rs755742671
NM_032387.5(WNK4):c.2080C>T (p.Gln694Ter)
NM_032387.5(WNK4):c.2095A>G (p.Lys699Glu)
NM_032387.5(WNK4):c.2110C>T (p.Arg704Ter)
NM_032387.5(WNK4):c.2155A>G (p.Met719Val)
NM_032387.5(WNK4):c.2185G>C (p.Glu729Gln)
NM_032387.5(WNK4):c.221C>T (p.Ser74Phe)
NM_032387.5(WNK4):c.2258G>A (p.Gly753Asp)
NM_032387.5(WNK4):c.2295+1G>A rs769831520
NM_032387.5(WNK4):c.2321T>C (p.Leu774Pro)
NM_032387.5(WNK4):c.2326G>A (p.Val776Ile)
NM_032387.5(WNK4):c.2527T>C (p.Phe843Leu)
NM_032387.5(WNK4):c.2536A>G (p.Ile846Val)
NM_032387.5(WNK4):c.2575A>C (p.Thr859Pro)
NM_032387.5(WNK4):c.2577C>T (p.Thr859=) rs387907558
NM_032387.5(WNK4):c.2629_2632del (p.Gln878fs)
NM_032387.5(WNK4):c.262G>C (p.Asp88His)
NM_032387.5(WNK4):c.268G>T (p.Ala90Ser)
NM_032387.5(WNK4):c.2718T>C (p.Phe906=) rs387907564
NM_032387.5(WNK4):c.2750C>T (p.Ser917Phe)
NM_032387.5(WNK4):c.2807C>T (p.Thr936Ile)
NM_032387.5(WNK4):c.2812G>T (p.Ala938Ser)
NM_032387.5(WNK4):c.2856TCC[1] (p.Pro954del)
NM_032387.5(WNK4):c.3088C>A (p.Pro1030Thr)
NM_032387.5(WNK4):c.3182G>C (p.Gly1061Ala)
NM_032387.5(WNK4):c.3187G>A (p.Gly1063Arg)
NM_032387.5(WNK4):c.318dup (p.Glu107fs)
NM_032387.5(WNK4):c.3293del (p.Gly1098fs) rs1315191413
NM_032387.5(WNK4):c.3307del (p.Pro1102_Leu1103insTer)
NM_032387.5(WNK4):c.3421C>G (p.Leu1141Val)
NM_032387.5(WNK4):c.3424C>T (p.Arg1142Trp)
NM_032387.5(WNK4):c.3425G>A (p.Arg1142Gln)
NM_032387.5(WNK4):c.3479T>C (p.Ile1160Thr)
NM_032387.5(WNK4):c.3490T>C (p.Tyr1164His)
NM_032387.5(WNK4):c.3503G>A (p.Gly1168Glu)
NM_032387.5(WNK4):c.3515C>T (p.Pro1172Leu)
NM_032387.5(WNK4):c.3519G>A (p.Pro1173=)
NM_032387.5(WNK4):c.3550A>G (p.Ser1184Gly)
NM_032387.5(WNK4):c.3559C>T (p.Arg1187Cys)
NM_032387.5(WNK4):c.3596G>A (p.Arg1199His)
NM_032387.5(WNK4):c.35T>G (p.Leu12Arg)
NM_032387.5(WNK4):c.3653dup (p.Ser1219fs)
NM_032387.5(WNK4):c.3673del (p.Ser1225fs)
NM_032387.5(WNK4):c.3709G>A (p.Ala1237Thr)
NM_032387.5(WNK4):c.3712G>A (p.Gly1238Arg)
NM_032387.5(WNK4):c.3715del (p.Asp1239fs)
NM_032387.5(WNK4):c.374C>G (p.Pro125Arg)
NM_032387.5(WNK4):c.37A>G (p.Met13Val)
NM_032387.5(WNK4):c.476A>G (p.Asp159Gly)
NM_032387.5(WNK4):c.484A>G (p.Thr162Ala)
NM_032387.5(WNK4):c.493G>T (p.Val165Leu)
NM_032387.5(WNK4):c.512G>A (p.Gly171Asp)
NM_032387.5(WNK4):c.531_532del (p.Ile178fs)
NM_032387.5(WNK4):c.546T>A (p.Arg182=) rs387907563
NM_032387.5(WNK4):c.550T>C (p.Ser184Pro)
NM_032387.5(WNK4):c.587C>A (p.Thr196Asn)
NM_032387.5(WNK4):c.622C>T (p.Arg208Trp)
NM_032387.5(WNK4):c.665_668dup (p.Glu223fs)
NM_032387.5(WNK4):c.673C>G (p.Leu225Val)
NM_032387.5(WNK4):c.692C>T (p.Pro231Leu)
NM_032387.5(WNK4):c.703C>T (p.Arg235Cys)
NM_032387.5(WNK4):c.704G>A (p.Arg235His)
NM_032387.5(WNK4):c.716C>G (p.Ser239Trp) rs199775692
NM_032387.5(WNK4):c.731T>C (p.Leu244Pro)
NM_032387.5(WNK4):c.776C>T (p.Ser259Leu) rs138156012
NM_032387.5(WNK4):c.82C>G (p.Leu28Val)

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