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Links from Gene

Items: 1 to 100 of 361

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WNK4
(L225V)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GUncertain significance
WNK4
(R45S)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GUncertain significance
WNK4
(R185H +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
WNK4
(Q33L)
Single nucleotide variant
(5 prime UTR variant +1 more)
WNK4-related disorder
GLikely benign
WNK4
(R1188H +1 more)
Single nucleotide variant
(missense variant)
WNK4-related disorder
GUncertain significance
WNK4
(T533fs +1 more)
Duplication
(frameshift variant)
not specified
GUncertain significance
WNK4
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GLikely benign
LOC126862568, WNK4
(E271V)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
WNK4
(P916L +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WNK4
(V1019M +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WNK4
(V760A +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WNK4
(S818F +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
LOC126862568, WNK4
(P274L)
Single nucleotide variant
(5 prime UTR variant +1 more)
Inborn genetic diseases
GUncertain significance
WNK4
(S4F)
Single nucleotide variant
(5 prime UTR variant +1 more)
Inborn genetic diseases
GUncertain significance
WNK4
(R58G)
Single nucleotide variant
(5 prime UTR variant +1 more)
Inborn genetic diseases
GUncertain significance
LOC126862568, WNK4
(S281N)
Single nucleotide variant
(5 prime UTR variant +1 more)
Inborn genetic diseases
GUncertain significance
WNK4
(A80T)
Single nucleotide variant
(5 prime UTR variant +1 more)
Inborn genetic diseases
GUncertain significance
WNK4
(L12F)
Single nucleotide variant
(5 prime UTR variant +1 more)
Inborn genetic diseases
GUncertain significance
WNK4
(R402W +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WNK4
(G902R +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WNK4
(E871K +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SLC4A1, DCAKD
+422 more
Copy number loss
Breast-ovarian cancer, familial, susceptibility to, 1
GPathogenic
WNK4
(T167K)
Single nucleotide variant
(5 prime UTR variant +1 more)
Inborn genetic diseases
GUncertain significance
WNK4
(M13R)
Single nucleotide variant
(5 prime UTR variant +1 more)
Inborn genetic diseases
GUncertain significance
WNK4
(M1181T +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WNK4
(A843S +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WNK4
(P842T +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WNK4
(G1174V +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WNK4
(R1166Q +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WNK4
(G704D +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WNK4
(R658Q +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WNK4
(R658W +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WNK4
(T550M +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
WNK4
(D88H)
Single nucleotide variant
(5 prime UTR variant +1 more)
Inborn genetic diseases
GUncertain significance
WNK4
(D85G)
Single nucleotide variant
(5 prime UTR variant +1 more)
Inborn genetic diseases
GUncertain significance
WNK4
(R368Q +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WNK4
(G270R +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WNK4
(R183Q +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WNK4
(R172C +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WNK4
(Q490R +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
LOC126862568, WNK4
(K387R +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WNK4
(P480R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
WNK4
Single nucleotide variant
(synonymous variant)
WNK4-related disorder
GLikely benign
WNK4
Single nucleotide variant
(synonymous variant)
WNK4-related disorder
GLikely benign
WNK4
Single nucleotide variant
(5 prime UTR variant +1 more)
WNK4-related disorder
GLikely benign
WNK4
Single nucleotide variant
(intron variant)
WNK4-related disorder
GLikely benign
WNK4
Single nucleotide variant
(5 prime UTR variant +1 more)
WNK4-related disorder
GLikely benign
WNK4, LOC126862568
Single nucleotide variant
(intron variant)
not provided
GBenign
WNK4
(A901T +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
WNK4
(D903fs +1 more)
Deletion
(frameshift variant)
not provided
GUncertain significance
WNK4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
WNK4
(A494G +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
WNK4
(P302R +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
WNK4
(Y1164H +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
WNK4
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GLikely benign
WNK4
Single nucleotide variant
(intron variant)
not provided
GLikely benign
WNK4
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
WNK4
Single nucleotide variant
(intron variant)
not provided
GLikely benign
WNK4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
WNK4
(R1142W +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
WNK4
(M13V)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GUncertain significance
WNK4
(E223fs)
Duplication
(5 prime UTR variant +1 more)
not provided
GUncertain significance
WNK4, LOC126862568
Single nucleotide variant
(intron variant)
not provided
GBenign
WNK4
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GBenign
WNK4
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
WNK4
Single nucleotide variant
(intron variant)
not provided
GLikely benign
WNK4
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GLikely benign
WNK4
Single nucleotide variant
(intron variant)
not provided
GLikely benign
WNK4
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GLikely benign
WNK4
(L28V)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GUncertain significance
WNK4
(S285L +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
WNK4
(P618del +1 more)
Microsatellite
(inframe_deletion)
not provided
GUncertain significance
WNK4
(I1160T +1 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
WNK4
(T859P +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
WNK4
(T936I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC126862568, WNK4
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GLikely benign
WNK4
(G48R)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GLikely benign
WNK4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LOC126862568, WNK4
(M1L +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
LOC126862568, WNK4
(R275Q)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GUncertain significance
WNK4
(R235H)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GUncertain significance
LOC126862568, WNK4
(R329L +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
WNK4
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GLikely benign
WNK4
(G320E +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC126862568, WNK4
(C364G +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
WNK4
(Q229P +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
WNK4
(R337* +1 more)
Single nucleotide variant
(nonsense)
not provided
GUncertain significance
WNK4
Single nucleotide variant
(intron variant)
not provided
GLikely benign
WNK4
(P451L +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
WNK4
Single nucleotide variant
(synonymous variant)
not provided
GBenign
WNK4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
WNK4
(S1219fs +1 more)
Duplication
(frameshift variant)
not provided
GUncertain significance
WNK4
(E393Q +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
WNK4
(E186* +1 more)
Single nucleotide variant
(nonsense)
not provided
GUncertain significance
WNK4
(P908L +1 more)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
WNK4
(E224del +1 more)
Microsatellite
(inframe_deletion)
WNK4-related disorder
GLikely pathogenic
WNK4
(L22M)
Single nucleotide variant
(5 prime UTR variant +1 more)
WNK4-related disorder
GUncertain significance
LOC126862568, WNK4
(G320E +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WNK4
(E434K +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WNK4
(P115R +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
Display optionsSort by RelevanceDownload
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