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Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AXL
(A79V)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
AXL
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign
AXL
Single nucleotide variant
(intron variant)
not specified
GUncertain significance
AXL
(Q361P +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GLikely benign
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