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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FBXL4
(R482W)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+3 more
GPathogenic/Likely pathogenic
FBXL4
(R435*)
Single nucleotide variant
(nonsense +1 more)
Inborn genetic diseases
+3 more
GPathogenic
FBXL4
(Y162*)
Single nucleotide variant
(nonsense +1 more)
Mitochondrial DNA depletion syndrome 13
+1 more
GPathogenic/Likely pathogenic
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