"PreventionGenetics, part of Exact Sciences"[submitter] AND "DLG5"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3050412	NM_004747.4(DLG5):c.3880G>T (p.Val1294Leu)	DLG5 (V1294L)	Single nucleotide variant (missense variant)	DLG5-related disorder	GLikely benign
Select item 2631079	NM_004747.4(DLG5):c.3431A>G (p.Glu1144Gly)	DLG5 (E1144G)	Single nucleotide variant (missense variant)	DLG5-related disorder	GUncertain significance
Select item 2633473	NM_004747.4(DLG5):c.2981G>A (p.Gly994Asp)	DLG5 (G994D)	Single nucleotide variant (missense variant)	DLG5-related disorder	GUncertain significance
Select item 2637058	NM_004747.4(DLG5):c.2737C>T (p.Arg913Trp)	DLG5 (R913W)	Single nucleotide variant (missense variant)	DLG5-related disorder	GUncertain significance
Select item 3047252	NM_004747.4(DLG5):c.2669G>A (p.Arg890His)	DLG5 (R890H)	Single nucleotide variant (missense variant)	DLG5-related disorder	GLikely benign
Select item 3054839	NM_004747.4(DLG5):c.389C>T (p.Ala130Val)	DLG5 (A130V)	Single nucleotide variant (missense variant)	DLG5-related disorder	GLikely benign
Select item 3043769	NM_004747.4(DLG5):c.268G>C (p.Gly90Arg)	DLG5 (G90R)	Single nucleotide variant (missense variant)	DLG5-related disorder	GUncertain significance

ClinVar