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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC120908923, LOC120947224
+1352 more
Copy number gain
See cases
GPathogenic
EXOC8
Deletion
(3 prime UTR variant)
not provided
GBenign
EXOC8
Deletion
(frameshift variant)
not provided
GLikely pathogenic
EXOC8
(S599fs)
Deletion
(frameshift variant)
not provided
GUncertain significance
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