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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CSTPP1
(R18Q)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
CSTPP1
Single nucleotide variant
(3 prime UTR variant +3 more)
not provided
GLikely benign
CSTPP1
(E328K +2 more)
Single nucleotide variant
(3 prime UTR variant +3 more)
not specified
GUncertain significance
CSTPP1
(S313L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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