"PreventionGenetics, part of Exact Sciences"[submitter] AND "TDP2"[gen - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 727113	NM_016614.3(TDP2):c.266A>G (p.Asn89Ser)	TDP2 (N89S)	Single nucleotide variant (missense variant)	TDP2-related disorder +1 more	GLikely benign
Select item 709650	NM_016614.3(TDP2):c.175A>G (p.Asn59Asp)	TDP2 (N59D)	Single nucleotide variant (missense variant)	TDP2-related disorder +1 more	GLikely benign
Select item 770922	NM_016614.3(TDP2):c.17G>T (p.Cys6Phe)	LOC113174982, TDP2 (C6F)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 730556	NM_016614.3(TDP2):c.9G>A (p.Leu3=)	LOC113174982, TDP2	Single nucleotide variant (synonymous variant)	TDP2-related disorder +1 more	GBenign/Likely benign
Select item 3038889	NM_016614.3(TDP2):c.-9G>A	LOC113174982, TDP2	Single nucleotide variant (5 prime UTR variant)	TDP2-related disorder	GLikely benign

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