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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ERCC8
(R198*)
Single nucleotide variant
(nonsense +1 more)
not provided
GUncertain significance
ERCC8
(F189L)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely benign