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Items: 13

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DCC
(S126*)
Single nucleotide variant
(nonsense)
Mirror movements 1
Gnot provided
DCC
(N176S)
Single nucleotide variant
(missense variant)
Mirror movements 1
Gnot provided
DCC
(V191fs)
Duplication
(frameshift variant)
Mirror movements 1
GPathogenic
DCC
(R275*)
Single nucleotide variant
(nonsense)
Corpus callosum, agenesis of
+1 more
GPathogenic
DCC
Single nucleotide variant
(splice donor variant)
not provided
GPathogenic
DCC
(R446fs)
Insertion
(frameshift variant)
Mirror movements 1
Gnot provided
DCC
(G470D)
Single nucleotide variant
(missense variant)
not provided
+1 more
GLikely benign
DCC
(R667H)
Single nucleotide variant
(missense variant)
not provided
GBenign/Likely benign
DCC
(N702S)
Single nucleotide variant
(missense variant)
DCC-related condition
+3 more
GConflicting classifications of pathogenicity
DCC
(G803R)
Single nucleotide variant
(missense variant)
Mirror movements 1
GUncertain significance
DCC
(P960fs)
Microsatellite
(frameshift variant)
Mirror movements 1
Gnot provided
DCC
(L1279fs)
Microsatellite
(frameshift variant)
Mirror movements 1
GPathogenic
DCC
Deletion
Mirror movements 1
GPathogenic
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