"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "GRIN2D"[ge - ClinVar

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Items: 53

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1910655	NM_000836.4(GRIN2D):c.102G>A (p.Gly34=)	GRIN2D	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 808606	NM_000836.4(GRIN2D):c.103C>T (p.Pro35Ser)	GRIN2D, LOC130064855 (P35S)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 2650198	NM_000836.4(GRIN2D):c.282G>A (p.Ser94=)	GRIN2D	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1694933	NM_000836.4(GRIN2D):c.358G>A (p.Asp120Asn)	GRIN2D (D120N)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 1468304	NM_000836.4(GRIN2D):c.412T>G (p.Ser138Ala)	GRIN2D, LOC130064856 (S138A)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1609411	NM_000836.4(GRIN2D):c.414G>A (p.Ser138=)	GRIN2D, LOC130064856	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1632739	NM_000836.4(GRIN2D):c.417G>A (p.Leu139=)	GRIN2D, LOC130064856	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 808607	NM_000836.4(GRIN2D):c.667C>G (p.Leu223Val)	GRIN2D (L223V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 789351	NM_000836.4(GRIN2D):c.723G>T (p.Ala241=)	GRIN2D	Single nucleotide variant (synonymous variant)	GRIN2D-related condition +1 more	GLikely benign
Select item 1985084	NM_000836.4(GRIN2D):c.749G>C (p.Arg250Pro)	GRIN2D (R250P)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 1176711	NM_000836.4(GRIN2D):c.750A>G (p.Arg250=)	GRIN2D	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1611859	NM_000836.4(GRIN2D):c.897C>G (p.Pro299=)	GRIN2D	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2650199	NM_000836.4(GRIN2D):c.1065C>T (p.His355=)	GRIN2D	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1298778	NM_000836.4(GRIN2D):c.1201-5C>T	GRIN2D	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1504372	NM_000836.4(GRIN2D):c.1387C>A (p.Arg463=)	GRIN2D	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 808608	NM_000836.4(GRIN2D):c.1434C>T (p.Arg478=)	GRIN2D	Single nucleotide variant (synonymous variant)	not provided	GConflicting classifications of pathogenicity
Select item 788837	NM_000836.4(GRIN2D):c.1551C>T (p.Ile517=)	GRIN2D	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1563012	NM_000836.4(GRIN2D):c.1629C>T (p.Asn543=)	GRIN2D	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2650200	NM_000836.4(GRIN2D):c.1848G>A (p.Leu616=)	GRIN2D	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 808609	NM_000836.4(GRIN2D):c.2024C>T (p.Ala675Val)	GRIN2D (A675V)	Single nucleotide variant (missense variant)	Developmental and epileptic encephalopathy, 46 +1 more	GConflicting classifications of pathogenicity
Select item 1013174	NM_000836.4(GRIN2D):c.2041A>G (p.Met681Val)	GRIN2D (M681V)	Single nucleotide variant (missense variant)	not provided	GPathogenic/Likely pathogenic
Select item 769978	NM_000836.4(GRIN2D):c.2271C>T (p.Ile757=)	GRIN2D	Single nucleotide variant (synonymous variant)	GRIN2D-related condition +1 more	GBenign/Likely benign
Select item 1013175	NM_000836.4(GRIN2D):c.2511C>A (p.Ser837Arg)	GRIN2D (S837R)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 2650201	NM_000836.4(GRIN2D):c.2604G>A (p.Leu868=)	GRIN2D	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2650202	NM_000836.4(GRIN2D):c.2712G>C (p.Pro904=)	GRIN2D	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2650203	NM_000836.4(GRIN2D):c.2727G>C (p.Pro909=)	GRIN2D	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2650204	NM_000836.4(GRIN2D):c.2782G>T (p.Gly928Trp)	GRIN2D (G928W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1411666	NM_000836.4(GRIN2D):c.2782G>A (p.Gly928Arg)	GRIN2D (G928R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1358430	NM_000836.4(GRIN2D):c.2852C>T (p.Pro951Leu)	GRIN2D (P951L)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 1559579	NM_000836.4(GRIN2D):c.2856G>C (p.Pro952=)	GRIN2D	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1346634	NM_000836.4(GRIN2D):c.2861G>T (p.Gly954Val)	GRIN2D (G954V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1879448	NM_000836.4(GRIN2D):c.2910G>T (p.Pro970=)	GRIN2D	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 774738	NM_000836.4(GRIN2D):c.2910G>A (p.Pro970=)	GRIN2D	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1675754	NM_000836.4(GRIN2D):c.3036C>G (p.Arg1012=)	GRIN2D	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1563492	NM_000836.4(GRIN2D):c.3105C>T (p.Ala1035=)	GRIN2D	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2053043	NM_000836.4(GRIN2D):c.3132A>C (p.Pro1044=)	GRIN2D	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1545379	NM_000836.4(GRIN2D):c.3154G>A (p.Asp1052Asn)	GRIN2D (D1052N)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GBenign/Likely benign
Select item 2650205	NM_000836.4(GRIN2D):c.3228G>C (p.Ala1076=)	GRIN2D	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2672780	NM_000836.4(GRIN2D):c.3235G>T (p.Ala1079Ser)	GRIN2D (A1079S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1176712	NM_000836.4(GRIN2D):c.3244A>G (p.Thr1082Ala)	GRIN2D (T1082A)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 1012454	NM_000836.4(GRIN2D):c.3260G>C (p.Gly1087Ala)	GRIN2D (G1087A)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1424539	NM_000836.4(GRIN2D):c.3277C>G (p.Pro1093Ala)	GRIN2D (P1093A)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 1567889	NM_000836.4(GRIN2D):c.3402C>T (p.Phe1134=)	GRIN2D	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1012455	NM_000836.4(GRIN2D):c.3529G>A (p.Ala1177Thr)	GRIN2D (A1177T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2766920	NM_000836.4(GRIN2D):c.3550G>A (p.Ala1184Thr)	GRIN2D (A1184T)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 1169577	NM_000836.4(GRIN2D):c.3657G>A (p.Leu1219=)	GRIN2D	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1390424	NM_000836.4(GRIN2D):c.3674G>T (p.Arg1225Leu)	GRIN2D (R1225L)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 1377325	NM_000836.4(GRIN2D):c.3706_3723del (p.Pro1236_Arg1241del)	GRIN2D	Deletion (inframe_deletion)	Developmental and epileptic encephalopathy, 46 +1 more	GConflicting classifications of pathogenicity
Select item 2650206	NM_000836.4(GRIN2D):c.3705C>A (p.Arg1235=)	GRIN2D	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 932433	NM_000836.4(GRIN2D):c.3750C>A (p.His1250Gln)	GRIN2D (H1250Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2650207	NM_000836.4(GRIN2D):c.3774G>T (p.Gly1258=)	GRIN2D	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1566103	NM_000836.4(GRIN2D):c.3789G>A (p.Pro1263=)	GRIN2D	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2650208	NM_000836.4(GRIN2D):c.3889T>C (p.Cys1297Arg)	GRIN2D (C1297R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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Items: 53