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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FTCD, FTCD-AS1
(K151M)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign
FTCD, FTCD-AS1
(G144R)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
FTCD, FTCD-AS1
(R142W)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
FTCD-AS1, FTCD
Single nucleotide variant
(synonymous variant)
Glutamate formiminotransferase deficiency
+2 more
GBenign
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