"PreventionGenetics, part of Exact Sciences"[submitter] AND "DLGAP1-AS - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3033733	NM_004746.4(DLGAP1):c.860G>A (p.Arg287Gln)	DLGAP1, DLGAP1-AS3 (R287Q)	Single nucleotide variant (missense variant)	DLGAP1-related disorder	GLikely benign
Select item 771503	NM_004746.4(DLGAP1):c.852C>A (p.Thr284=)	DLGAP1, DLGAP1-AS3	Single nucleotide variant (synonymous variant)	DLGAP1-related disorder +1 more	GBenign
Select item 3051867	NM_004746.4(DLGAP1):c.421C>T (p.Leu141=)	DLGAP1, DLGAP1-AS3	Single nucleotide variant (synonymous variant)	DLGAP1-related disorder	GLikely benign
Select item 3054401	NM_004746.4(DLGAP1):c.406G>A (p.Gly136Ser)	DLGAP1, DLGAP1-AS3 (G136S)	Single nucleotide variant (missense variant)	DLGAP1-related disorder	GLikely benign
Select item 3038851	NM_004746.4(DLGAP1):c.345C>T (p.Arg115=)	DLGAP1, DLGAP1-AS3	Single nucleotide variant (synonymous variant)	DLGAP1-related disorder	GLikely benign
Select item 3053483	NM_004746.4(DLGAP1):c.57C>A (p.Ala19=)	DLGAP1, DLGAP1-AS3	Single nucleotide variant (synonymous variant)	DLGAP1-related disorder	GLikely benign

ClinVar