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Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KANSL1
(R1026G +11 more)
Single nucleotide variant
(missense variant)
Koolen-de Vries syndrome
GUncertain significance
KANSL1
(R1010* +1 more)
Single nucleotide variant
(nonsense)
Koolen-de Vries syndrome
GPathogenic/Likely pathogenic
KANSL1
(R443K +9 more)
Single nucleotide variant
(missense variant)
Koolen-de Vries syndrome
GUncertain significance
KANSL1
(S335G +4 more)
Single nucleotide variant
(missense variant)
Koolen-de Vries syndrome
GUncertain significance
KANSL1
(T732A)
Single nucleotide variant
(missense variant)
Koolen-de Vries syndrome
+2 more
GConflicting classifications of pathogenicity
KANSL1
(H258Q +2 more)
Single nucleotide variant
(missense variant)
Koolen-de Vries syndrome
GUncertain significance
KANSL1
(R592W)
Single nucleotide variant
(missense variant)
Koolen-de Vries syndrome
+1 more
GConflicting classifications of pathogenicity
KANSL1
(A169T +2 more)
Single nucleotide variant
(missense variant)
Koolen-de Vries syndrome
GUncertain significance
KANSL1
(L270fs)
Deletion
(frameshift variant)
Koolen-de Vries syndrome
+4 more
GConflicting classifications of pathogenicity
KANSL1
(V261fs)
Duplication
(frameshift variant)
Koolen-de Vries syndrome
+1 more
GUncertain significance
KANSL1
(Q116K)
Single nucleotide variant
(missense variant)
Koolen-de Vries syndrome
GUncertain significance
KANSL1
(Q99*)
Single nucleotide variant
(nonsense)
Koolen-de Vries syndrome
GLikely pathogenic
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