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

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 376909	NM_014026.6(DCPS):c.677G>A (p.Gly226Asp)	DCPS, GSEC (G226D +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign/Likely benign
Select item 732989	NM_014026.6(DCPS):c.717G>A (p.Pro239=)	DCPS, GSEC	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 749774	NM_014026.6(DCPS):c.804C>T (p.His268=)	DCPS, GSEC	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 782778	NM_014026.6(DCPS):c.868T>G (p.Ser290Ala)	DCPS, GSEC (S290A +1 more)	Single nucleotide variant (missense variant)	DCPS-related disorder +1 more	GLikely benign
Select item 775095	NM_014026.6(DCPS):c.1013G>A (p.Ter338=)	DCPS, GSEC	Single nucleotide variant (synonymous variant)	DCPS-related disorder +1 more	GBenign/Likely benign

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