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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
UNG
(P122fs +1 more)
Deletion
(frameshift variant)
Hyper-IgM syndrome type 5
GPathogenic
UNG
(I134fs +1 more)
Deletion
(frameshift variant)
Hyper-IgM syndrome type 5
GPathogenic
UNG
(E182fs +1 more)
Microsatellite
(frameshift variant)
Hyper-IgM syndrome type 5
GPathogenic
UNG
(F251S +1 more)
Single nucleotide variant
(missense variant)
Hyper-IgM syndrome type 5
GPathogenic
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