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Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MAP2K2
(R388W)
Single nucleotide variant
(missense variant)
RASopathy
GBenign
MAP2K2
(A355V)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+3 more
GUncertain significance
MAP2K2
Single nucleotide variant
(intron variant)
Cardiofaciocutaneous syndrome 4
+2 more
GBenign
MAP2K2
Single nucleotide variant
(intron variant)
RASopathy
GLikely benign
MAP2K2
(G302R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MAP2K2
(R297Q)
Single nucleotide variant
(missense variant)
Cardiofaciocutaneous syndrome 4
+2 more
GUncertain significance
MAP2K2
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
MAP2K2
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GConflicting classifications of pathogenicity
MAP2K2
Single nucleotide variant
(intron variant)
RASopathy
GBenign
MAP2K2
Single nucleotide variant
(synonymous variant)
RASopathy
GBenign
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