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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCYL1
(Q57*)
Single nucleotide variant
(nonsense)
CALFAN syndrome
+1 more
GPathogenic
SCYL1
(E86*)
Single nucleotide variant
(nonsense)
CALFAN syndrome
GPathogenic
SCYL1
(A105V)
Single nucleotide variant
(missense variant)
CALFAN syndrome
+1 more
GPathogenic
SCYL1
(D478G)
Single nucleotide variant
(missense variant)
CALFAN syndrome
+1 more
GPathogenic
SCYL1
(Q628* +1 more)
Single nucleotide variant
(nonsense)
CALFAN syndrome
+1 more
GPathogenic
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