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Items: 99

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATP9B
(D3Y)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(I5N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(I5S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(P6L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(P9L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(R11C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(A14P)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
ATP9B
(R22L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(A24V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(S27I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(R37W)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(A48V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(H49L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(G61R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(E65K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(R74Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(G91S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(I104V)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
ATP9B
(R116H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(T117P)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(T117I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
ATP9B
(A184T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(R196W)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(R196Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(R204H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(R207H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(V240M)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(S248L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(L277V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(A280V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(D308N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(D308G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(R318K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(I351L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(T353A)
Single nucleotide variant
(missense variant +1 more)
not specified
+1 more
GUncertain significance
ATP9B
(R379Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
ATP9B
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
ATP9B
(L409F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(R425H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(M438V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(R482Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
ATP9B
(M495V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(D504N)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
ATP9B
(A513T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(A513D)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely benign
ATP9B
(R561Q)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely benign
ATP9B
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
ATP9B
(N581S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(V592I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(A593T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(E636K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(V644I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(V661M)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(V667M)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(R686W)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(V689M)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(T696I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
Single nucleotide variant
(intron variant)
not provided
GBenign
ATP9B
(L719F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(K720R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(A723T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(A723V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(D742E)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(L744M)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(R756C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(A758T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(R793K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(T796N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(R798W)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(A801P)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(L803S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ATP9B
(E836D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(R848C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(T852I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(R856L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(R868H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(I891F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(I891T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(A899V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(F910L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(L965F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(E990D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(M991V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(P996L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
ATP9B
(L1034V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(V1042M)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(A1044V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(A1049T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(V1071A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(A1085T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
(A1085P)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
ATP9B
(R1135H +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ATP9B
Copy number loss
not provided
GLikely benign
Display optionsSort by LocationDownload
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