"PreventionGenetics, part of Exact Sciences"[submitter] AND "TSEN34"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2965130	NM_001077446.4(TSEN34):c.177C>G (p.Leu59=)	TSEN34	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3054937	NM_001077446.4(TSEN34):c.488-9C>T	TSEN34	Single nucleotide variant (intron variant)	TSEN34-related disorder	GLikely benign
Select item 137754	NM_001077446.4(TSEN34):c.688C>A (p.Arg230=)	TSEN34	Single nucleotide variant (synonymous variant)	Pontoneocerebellar hypoplasia +2 more	GBenign
Select item 382027	NM_001077446.4(TSEN34):c.786C>T (p.Cys262=)	TSEN34	Single nucleotide variant (synonymous variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 261679	NM_001077446.4(TSEN34):c.*29G>A	TSEN34	Single nucleotide variant (3 prime UTR variant +1 more)	not specified +2 more	GBenign
Select item 3034728	NM_001077446.4(TSEN34):c.*262T>C	TSEN34 (F298L)	Single nucleotide variant (3 prime UTR variant +1 more)	TSEN34-related disorder	GBenign

ClinVar