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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KRAS
(D153V)
Single nucleotide variant
(3 prime UTR variant +1 more)
Noonan syndrome
GPathogenic
KRAS
(I187V)
Single nucleotide variant
(missense variant +1 more)
Autoimmune lymphoproliferative syndrome type 4
GUncertain significance
KRAS
Single nucleotide variant
(no sequence alteration +1 more)
Cardiovascular phenotype
+2 more
GBenign
KRAS
(D119N)
Single nucleotide variant
(missense variant)
Autoimmune lymphoproliferative syndrome type 4
+5 more
GLikely pathogenic
KRAS
(R68W)
Single nucleotide variant
(missense variant)
Noonan syndrome 3
GLikely pathogenic
KRAS
(S65I)
Single nucleotide variant
(missense variant)
RASopathy
GLikely pathogenic
KRAS
(P34R)
Single nucleotide variant
(missense variant)
RASopathy
+7 more
GPathogenic/Likely pathogenic
KRAS
(V14I)
Single nucleotide variant
(missense variant)
Noonan syndrome
GPathogenic
KRAS
(K5E)
Single nucleotide variant
(missense variant)
RASopathy
+4 more
GPathogenic/Likely pathogenic
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