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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARID1B
(G544fs)
Deletion
(frameshift variant)
ARID1B-related BAFopathy
+2 more
GPathogenic/Likely pathogenic
ARID1B
(Q118* +5 more)
Single nucleotide variant
(nonsense)
Coffin-Siris syndrome 1
GPathogenic
ARID1B
(N1025I +2 more)
Single nucleotide variant
(missense variant)
Coffin-Siris syndrome 1
GUncertain significance
ARID1B
Single nucleotide variant
(splice acceptor variant)
Coffin-Siris syndrome 1
GLikely pathogenic
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