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Items: 3

  • Unknown field was ignored: [Variant ID].
Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TP53
(R183L +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome
GUncertain significance
TP53
(R210Q +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome 1
GLikely benign
TP53
(R210P +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome 1
+3 more
GPathogenic/Likely pathogenic
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