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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 712729	NM_014026.6(DCPS):c.558G>A (p.Ala186=)	DCPS	Single nucleotide variant (synonymous variant)	DCPS-related disorder +1 more	GBenign/Likely benign
Select item 3053739	NM_014026.6(DCPS):c.636+5A>C	DCPS	Single nucleotide variant (intron variant)	DCPS-related disorder	GLikely benign
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

ClinVar