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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARID1B
(S525fs)
Deletion
(frameshift variant)
Coffin-Siris syndrome 1
GPathogenic
ARID1B
(S1134* +4 more)
Single nucleotide variant
(nonsense)
Coffin-Siris syndrome 1
GLikely pathogenic
ARID1B
(P502fs +3 more)
Duplication
(frameshift variant)
Coffin-Siris syndrome 1
GPathogenic
ARID1B
(E1828K +4 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
ARID1B
Deletion
(frameshift variant)
Coffin-Siris syndrome 1
GPathogenic
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