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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SATB2
(Q409R)
Single nucleotide variant
(missense variant)
Chromosome 2q32-q33 deletion syndrome
GLikely pathogenic
SATB2
(V368fs)
Deletion
(frameshift variant)
Chromosome 2q32-q33 deletion syndrome
GPathogenic
SATB2
(E185fs)
Insertion
(frameshift variant)
Chromosome 2q32-q33 deletion syndrome
GPathogenic
SATB2
(Y75*)
Single nucleotide variant
(nonsense +1 more)
Chromosome 2q32-q33 deletion syndrome
GPathogenic
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