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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADD3
(P7T +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
(T137I +1 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
ADD3
(G100D +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
(D259G +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ADD3
(T299I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
(L303S +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
(S396L +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
(Q503E +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ABLIM1, ABRAXAS2
+201 more
Copy number gain
See cases
GPathogenic
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