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Items: 8

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PCDH12
(S1140L)
Single nucleotide variant
(missense variant)
Diencephalic-mesencephalic junction dysplasia syndrome 1
GUncertain significance
PCDH12
(A1135V)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
PCDH12, RNF14
(E1015K)
Single nucleotide variant
(missense variant)
Diencephalic-mesencephalic junction dysplasia syndrome 1
GUncertain significance
PCDH12, RNF14
(Q855*)
Single nucleotide variant
(nonsense)
Diencephalic-mesencephalic junction dysplasia syndrome 1
GPathogenic
RNF14, PCDH12
(P684H)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
PCDH12, RNF14
(V658I)
Single nucleotide variant
(missense variant)
Diencephalic-mesencephalic junction dysplasia syndrome 1
+1 more
GUncertain significance
PCDH12, RNF14
(S361*)
Single nucleotide variant
(nonsense)
Diencephalic-mesencephalic junction dysplasia syndrome 1
GLikely pathogenic
PCDH12, RNF14
(R308*)
Single nucleotide variant
(nonsense)
Diencephalic-mesencephalic junction dysplasia syndrome 1
+1 more
GPathogenic/Likely pathogenic
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