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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYCN, MYCNOS
(Q22*)
Single nucleotide variant
(5 prime UTR variant +1 more)
Feingold syndrome type 1
Gnot provided
MYCN
(R322* +1 more)
Single nucleotide variant
(nonsense +1 more)
Feingold syndrome type 1
GPathogenic
MYCN
(S158fs +1 more)
Microsatellite
(frameshift variant +1 more)
Feingold syndrome type 1
Gnot provided
MYCN
(R373* +1 more)
Single nucleotide variant
(nonsense +1 more)
not provided
GPathogenic
MYCN
(R393H +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GPathogenic
MYCN
(R394H +1 more)
Single nucleotide variant
(missense variant +1 more)
Feingold syndrome type 1
GPathogenic
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