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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KRAS
(R167T)
Single nucleotide variant
(missense variant +1 more)
Noonan syndrome
GLikely benign
KRAS
(E153A)
Single nucleotide variant
(missense variant +1 more)
Noonan syndrome
GLikely pathogenic
KRAS
(T74I)
Single nucleotide variant
(missense variant)
Noonan syndrome
GLikely pathogenic
KRAS
(I55S)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
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