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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ANKRD11
(Q2443*)
Single nucleotide variant
(nonsense)
Inborn genetic diseases
+1 more
GPathogenic
ANKRD11
(K1387R)
Single nucleotide variant
(missense variant)
KBG syndrome
GUncertain significance
ANKRD11
(S872fs)
Microsatellite
(frameshift variant)
KBG syndrome
+1 more
GPathogenic/Likely pathogenic
ANKRD11
(S584C)
Single nucleotide variant
(missense variant)
KBG syndrome
GUncertain significance
ANKRD11
(D491Y)
Single nucleotide variant
(missense variant)
KBG syndrome
GUncertain significance
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