"PreventionGenetics, part of Exact Sciences"[submitter] AND "GRIN2D"[g - ClinVar

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Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3041310	NM_000836.4(GRIN2D):c.65T>A (p.Leu22Gln)	GRIN2D (L22Q)	Single nucleotide variant (missense variant)	GRIN2D-related disorder	GLikely benign
Select item 3042328	NM_000836.4(GRIN2D):c.70T>A (p.Cys24Ser)	GRIN2D (C24S)	Single nucleotide variant (missense variant)	GRIN2D-related disorder	GLikely benign
Select item 3032552	NM_000836.4(GRIN2D):c.198G>C (p.Ala66=)	GRIN2D, LOC130064855	Single nucleotide variant (synonymous variant)	GRIN2D-related disorder	GLikely benign
Select item 3047836	NM_000836.4(GRIN2D):c.204C>T (p.Arg68=)	GRIN2D	Single nucleotide variant (synonymous variant)	GRIN2D-related disorder	GLikely benign
Select item 3036553	NM_000836.4(GRIN2D):c.207G>A (p.Leu69=)	GRIN2D	Single nucleotide variant (synonymous variant)	GRIN2D-related disorder	GLikely benign
Select item 1940783	NM_000836.4(GRIN2D):c.354A>G (p.Glu118=)	GRIN2D	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1917830	NM_000836.4(GRIN2D):c.578G>A (p.Arg193His)	GRIN2D (R193H)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 789351	NM_000836.4(GRIN2D):c.723G>T (p.Ala241=)	GRIN2D	Single nucleotide variant (synonymous variant)	GRIN2D-related disorder +1 more	GLikely benign
Select item 745839	NM_000836.4(GRIN2D):c.1641C>T (p.Ser547=)	GRIN2D	Single nucleotide variant (synonymous variant)	GRIN2D-related disorder +1 more	GBenign/Likely benign
Select item 3031480	NM_000836.4(GRIN2D):c.1877C>G (p.Thr626Ser)	GRIN2D, LOC130064857 (T626S)	Single nucleotide variant (missense variant)	GRIN2D-related disorder	GUncertain significance
Select item 1636880	NM_000836.4(GRIN2D):c.1905G>T (p.Leu635=)	GRIN2D, LOC130064857	Single nucleotide variant (synonymous variant)	GRIN2D-related disorder +1 more	GLikely benign
Select item 727458	NM_000836.4(GRIN2D):c.1998C>T (p.Ala666=)	GRIN2D, LOC130064857	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 3038373	NM_000836.4(GRIN2D):c.2112G>T (p.Gln704His)	GRIN2D (Q704H)	Single nucleotide variant (missense variant)	GRIN2D-related disorder	GUncertain significance
Select item 1580197	NM_000836.4(GRIN2D):c.2181C>T (p.Pro727=)	GRIN2D	Single nucleotide variant (synonymous variant)	GRIN2D-related disorder +1 more	GLikely benign
Select item 769978	NM_000836.4(GRIN2D):c.2271C>T (p.Ile757=)	GRIN2D	Single nucleotide variant (synonymous variant)	GRIN2D-related disorder +1 more	GBenign/Likely benign
Select item 1948185	NM_000836.4(GRIN2D):c.2413C>T (p.Leu805=)	GRIN2D	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2630182	NM_000836.4(GRIN2D):c.2563G>T (p.Ala855Ser)	GRIN2D (A855S)	Single nucleotide variant (missense variant)	GRIN2D-related disorder	GUncertain significance
Select item 3052191	NM_000836.4(GRIN2D):c.2589C>T (p.Phe863=)	GRIN2D	Single nucleotide variant (synonymous variant)	GRIN2D-related disorder	GLikely benign
Select item 445447	NM_000836.4(GRIN2D):c.2765C>T (p.Ala922Val)	GRIN2D (A922V)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 774738	NM_000836.4(GRIN2D):c.2910G>A (p.Pro970=)	GRIN2D	Single nucleotide variant (synonymous variant)	GRIN2D-related disorder +1 more	GBenign/Likely benign
Select item 1878541	NM_000836.4(GRIN2D):c.3340G>A (p.Asp1114Asn)	GRIN2D (D1114N)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 2632511	NM_000836.4(GRIN2D):c.3512C>T (p.Pro1171Leu)	GRIN2D (P1171L)	Single nucleotide variant (missense variant)	GRIN2D-related disorder	GUncertain significance
Select item 2629396	NM_000836.4(GRIN2D):c.3518G>C (p.Ser1173Thr)	GRIN2D (S1173T)	Single nucleotide variant (missense variant)	GRIN2D-related disorder	GUncertain significance
Select item 2125635	NM_000836.4(GRIN2D):c.3560A>G (p.Glu1187Gly)	GRIN2D (E1187G)	Single nucleotide variant (missense variant)	GRIN2D-related disorder +1 more	GUncertain significance
Select item 1174759	NM_000836.4(GRIN2D):c.3628C>T (p.Pro1210Ser)	GRIN2D (P1210S)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1462409	NM_000836.4(GRIN2D):c.3637C>T (p.Pro1213Ser)	GRIN2D (P1213S)	Single nucleotide variant (missense variant)	GRIN2D-related disorder +1 more	GUncertain significance
Select item 765349	NM_000836.4(GRIN2D):c.3807G>C (p.Ser1269=)	GRIN2D	Single nucleotide variant (synonymous variant)	GRIN2D-related disorder +1 more	GLikely benign
Select item 2633829	NM_000836.4(GRIN2D):c.3812C>G (p.Ser1271Trp)	GRIN2D (S1271W)	Single nucleotide variant (missense variant)	GRIN2D-related disorder	GUncertain significance
Select item 2631102	NM_000836.4(GRIN2D):c.3863C>G (p.Thr1288Ser)	GRIN2D (T1288S)	Single nucleotide variant (missense variant)	GRIN2D-related disorder	GUncertain significance

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Items: 29