"PreventionGenetics, part of Exact Sciences"[submitter] AND "CTDSP2"[g - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3033573	NM_005730.4(CTDSP2):c.786C>T (p.Tyr262=)	CTDSP2	Single nucleotide variant (synonymous variant)	CTDSP2-related condition	GLikely benign
Select item 3034914	NM_005730.4(CTDSP2):c.768C>T (p.Ser256=)	CTDSP2	Single nucleotide variant (synonymous variant)	CTDSP2-related condition	GLikely benign
Select item 3051125	NM_005730.4(CTDSP2):c.747C>A (p.Ile249=)	CTDSP2	Single nucleotide variant (synonymous variant)	CTDSP2-related condition	GLikely benign

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