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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TP63
(R266Q +3 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic/Likely pathogenic
TP63
(R343Q +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+3 more
GPathogenic/Likely pathogenic
TP63
(A352E +3 more)
Single nucleotide variant
(missense variant)
TP63-Related Spectrum Disorders
+1 more
GLikely pathogenic
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