C5561951[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2585655	NM_005427.4(TP73):c.-20C>T	TP73	Single nucleotide variant (5 prime UTR variant)	Ciliary dyskinesia, primary, 47, and lissencephaly	GBenign
Select item 2585656	NM_005427.4(TP73):c.519C>T (p.Thr173=)	TP73	Single nucleotide variant (synonymous variant)	Ciliary dyskinesia, primary, 47, and lissencephaly	GBenign
Select item 2585657	NM_005427.4(TP73):c.985+15A>G	TP73	Single nucleotide variant (intron variant)	Ciliary dyskinesia, primary, 47, and lissencephaly	GBenign

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