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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SOS1
Single nucleotide variant
(intron variant)
Noonan syndrome 4
+3 more
GBenign
BRAF
(K601T +7 more)
Single nucleotide variant
(missense variant)
RASopathy
GPathogenic
BRAF
(G596V +7 more)
Single nucleotide variant
(missense variant)
RASopathy
GPathogenic
BRAF
(E501A +7 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic
BRAF
(F247L +4 more)
Single nucleotide variant
(missense variant)
Noonan syndrome and Noonan-related syndrome
GPathogenic
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