C4310687[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1031671	NM_000836.4(GRIN2D):c.838G>A (p.Ala280Thr)	GRIN2D (A280T)	Single nucleotide variant (missense variant)	Developmental and epileptic encephalopathy, 46 +1 more	GUncertain significance
Select item 1031669	NM_000836.4(GRIN2D):c.1085+13G>A	GRIN2D	Single nucleotide variant (intron variant)	Developmental and epileptic encephalopathy, 46	GUncertain significance
Select item 1029953	NM_000836.4(GRIN2D):c.2356A>G (p.Thr786Ala)	GRIN2D (T786A)	Single nucleotide variant (missense variant)	Developmental and epileptic encephalopathy, 46	GUncertain significance
Select item 1031670	NM_000836.4(GRIN2D):c.2611T>C (p.Trp871Arg)	GRIN2D (W871R)	Single nucleotide variant (missense variant)	Developmental and epileptic encephalopathy, 46 +1 more	GUncertain significance
Select item 1029954	NM_000836.4(GRIN2D):c.3076G>A (p.Gly1026Ser)	GRIN2D (G1026S)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1029955	NM_000836.4(GRIN2D):c.3888G>C (p.Arg1296Ser)	GRIN2D (R1296S)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GUncertain significance
Select item 1029956	NM_000836.4(GRIN2D):c.3929C>T (p.Ala1310Val)	GRIN2D (A1310V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance

ClinVar