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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NIPBL
(Y510*)
Single nucleotide variant
(nonsense)
Cornelia de Lange syndrome 1
GPathogenic
NIPBL
(M1071I)
Single nucleotide variant
(missense variant)
Cornelia de Lange syndrome 1
GUncertain significance
NIPBL
(N1823D)
Single nucleotide variant
(missense variant)
Cornelia de Lange syndrome 1
GLikely pathogenic
NIPBL
(R2298H)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic/Likely pathogenic
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