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Items: 14

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CUX1
Single nucleotide variant
(splice donor variant)
Global developmental delay with or without impaired intellectual development
GLikely pathogenic
CUX1
(R421W +1 more)
Single nucleotide variant
(intron variant +1 more)
Global developmental delay with or without impaired intellectual development
GUncertain significance
CUX1
(P527L +1 more)
Single nucleotide variant
(missense variant +1 more)
Global developmental delay with or without impaired intellectual development
GUncertain significance
CUX1
(E547D +1 more)
Single nucleotide variant
(missense variant +1 more)
Global developmental delay with or without impaired intellectual development
GUncertain significance
CUX1
(D801N +1 more)
Single nucleotide variant
(missense variant +1 more)
Global developmental delay with or without impaired intellectual development
GUncertain significance
CUX1
(S1093G +1 more)
Single nucleotide variant
(missense variant +1 more)
Global developmental delay with or without impaired intellectual development
GUncertain significance
CUX1
(P1124L +1 more)
Single nucleotide variant
(missense variant +1 more)
Global developmental delay with or without impaired intellectual development
GUncertain significance
CUX1
(G1317S +1 more)
Single nucleotide variant
(missense variant +1 more)
Global developmental delay with or without impaired intellectual development
GUncertain significance
CUX1
(R1325P +1 more)
Single nucleotide variant
(missense variant +1 more)
Global developmental delay with or without impaired intellectual development
GUncertain significance
CUX1
(A1330V +1 more)
Single nucleotide variant
(missense variant +1 more)
Global developmental delay with or without impaired intellectual development
GUncertain significance
CUX1
(P1376L +1 more)
Single nucleotide variant
(missense variant +1 more)
Global developmental delay with or without impaired intellectual development
GUncertain significance
CUX1
(A1386L +1 more)
Indel
(missense variant +1 more)
Global developmental delay with or without impaired intellectual development
GUncertain significance
CUX1
(A1433G +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
CUX1
(S1446G +1 more)
Single nucleotide variant
(missense variant +1 more)
Global developmental delay with or without impaired intellectual development
GUncertain significance
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