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Items: 17

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KAT6B
(R406Q)
Single nucleotide variant
(missense variant +1 more)
Genitopatellar syndrome
+1 more
GUncertain significance
KAT6B
(S504R)
Single nucleotide variant
(missense variant +1 more)
KAT6B-related disorder
+2 more
GConflicting classifications of pathogenicity
KAT6B
(I593T)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
KAT6B
(R363Q +4 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
KAT6B
(S119N +4 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
KAT6B
(R118C +7 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KAT6B
(M187V +7 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KAT6B
(E1099fs +7 more)
Deletion
(frameshift variant)
not provided
GPathogenic
KAT6B
(E1181D +7 more)
Single nucleotide variant
(missense variant)
Genitopatellar syndrome
+2 more
GConflicting classifications of pathogenicity
KAT6B
(R1049H +7 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
KAT6B
(E1115* +7 more)
Duplication
(nonsense)
not provided
GLikely pathogenic
KAT6B
(G1035R +7 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KAT6B
(S1075T +7 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KAT6B
(A1838S +7 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KAT6B
(V1087I +7 more)
Single nucleotide variant
(missense variant)
Genitopatellar syndrome
+1 more
GUncertain significance
KAT6B
(M1191L +7 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KAT6B
(M1232I +7 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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