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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FOXP2
(L121F +1 more)
Single nucleotide variant
(missense variant +1 more)
Childhood apraxia of speech
GUncertain significance
FOXP2
(Q230H +3 more)
Single nucleotide variant
(missense variant +1 more)
Childhood apraxia of speech
GUncertain significance
FOXP2
(V334L +4 more)
Single nucleotide variant
(missense variant +1 more)
Childhood apraxia of speech
+1 more
GUncertain significance
FOXP2
(R461C +4 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
FOXP2
(I506M +4 more)
Single nucleotide variant
(missense variant +1 more)
Childhood apraxia of speech
GUncertain significance
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