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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FGF14
(T106fs +8 more)
Deletion
(frameshift variant)
not provided
GPathogenic/Likely pathogenic
FGF14
(P24L +7 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
FGF14
(Q117R +8 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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