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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CBL
(M119I)
Single nucleotide variant
(missense variant)
not specified
+2 more
GUncertain significance
CBL
(Y371H)
Single nucleotide variant
(missense variant)
CBL-related disorder
+4 more
GPathogenic
CBL
(P703A)
Single nucleotide variant
(missense variant)
not specified
+1 more
GConflicting classifications of pathogenicity
CBL
(C840S)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
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