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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KRAS
(R164*)
Single nucleotide variant
(3 prime UTR variant +1 more)
Noonan syndrome 3
GLikely benign
PTPN11
(Y63C +1 more)
Single nucleotide variant
(missense variant)
Noonan syndrome
GPathogenic
PTPN11
(Q79R +1 more)
Single nucleotide variant
(missense variant)
Noonan syndrome and Noonan-related syndrome
+11 more
GPathogenic
PTPN11
(N308S +1 more)
Single nucleotide variant
(missense variant)
Juvenile myelomonocytic leukemia
+10 more
GPathogenic
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