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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RAF1
(R398L +5 more)
Single nucleotide variant
(missense variant +1 more)
RASopathy
GUncertain significance
RAF1
(G169R +1 more)
Single nucleotide variant
(missense variant +1 more)
RASopathy
+4 more
GPathogenic/Likely pathogenic
RAF1
(Q11K +1 more)
Single nucleotide variant
(missense variant +1 more)
LEOPARD syndrome 2
+2 more
GUncertain significance
RAF1
(I11F)
Single nucleotide variant
(missense variant +2 more)
Noonan syndrome 5
+5 more
GUncertain significance
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