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Items: 35

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ALX4
(A405G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALX4
(M398R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALX4
(A394T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALX4
(R388H)
Single nucleotide variant
(missense variant)
Parietal foramina 2
+1 more
GUncertain significance
ALX4
(E385Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALX4
(E381G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALX4
(S357N)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALX4
(S357G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALX4
(P334L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALX4
(G310S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALX4
(R296Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
ALX4
(Y289C)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALX4
(R282Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALX4
(R265*)
Single nucleotide variant
(nonsense)
Inborn genetic diseases
+1 more
GPathogenic
ALX4
(S209R)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ALX4
(P190H)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALX4
(P190L)
Single nucleotide variant
(missense variant)
Parietal foramina 2
+1 more
GUncertain significance
ALX4
(A185V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALX4
(D176G)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ALX4
(D169N)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALX4
(L166S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
ALX4
(E158D)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GBenign/Likely benign
ALX4
(C154S)
Single nucleotide variant
(missense variant)
not provided
+1 more
GLikely benign
ALX4
(T131A)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALX4
(Q125E)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALX4
(L124V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALX4
(H121Y)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALX4
(P116R)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
ALX4
Deletion
(inframe_deletion)
not provided
+1 more
GUncertain significance
ALX4
(P112L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALX4
(Q104P)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
ALX4
(Q98K)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALX4
(P92T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALX4
(G85S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
ALX4
(N2S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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