ClinVar for Gene (Select 116444) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3282815	NM_138690.3(GRIN3B):c.422C>T (p.Ala141Val)	GRIN3B (A141V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282814	NM_138690.3(GRIN3B):c.1034C>T (p.Thr345Met)	GRIN3B (T345M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282812	NM_138690.3(GRIN3B):c.754G>A (p.Val252Ile)	GRIN3B (V252I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282811	NM_138690.3(GRIN3B):c.1193C>T (p.Pro398Leu)	GRIN3B (P398L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282810	NM_138690.3(GRIN3B):c.1799C>A (p.Pro600His)	GRIN3B (P600H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282809	NM_138690.3(GRIN3B):c.889G>A (p.Val297Met)	GRIN3B (V297M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282808	NM_138690.3(GRIN3B):c.208C>G (p.Leu70Val)	GRIN3B (L70V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282807	NM_138690.3(GRIN3B):c.1817G>T (p.Arg606Leu)	GRIN3B (R606L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282806	NM_138690.3(GRIN3B):c.265C>G (p.Arg89Gly)	GRIN3B (R89G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282805	NM_138690.3(GRIN3B):c.914G>A (p.Gly305Asp)	GRIN3B (G305D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282804	NM_138690.3(GRIN3B):c.1385C>T (p.Ala462Val)	GRIN3B (A462V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282802	NM_138690.3(GRIN3B):c.1774C>T (p.Leu592Phe)	GRIN3B (L592F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282801	NM_138690.3(GRIN3B):c.1526G>A (p.Arg509Gln)	GRIN3B (R509Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282800	NM_138690.3(GRIN3B):c.920C>T (p.Ala307Val)	GRIN3B (A307V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282799	NM_138690.3(GRIN3B):c.2703C>T (p.Ser901=)	GRIN3B	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3282798	NM_138690.3(GRIN3B):c.476T>C (p.Leu159Pro)	GRIN3B (L159P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3242273	GRCh37/hg19 19p13.3(chr19:916637-1275315)x1	ABCA7, ARHGAP45 +14 more	Copy number loss	not provided	GPathogenic
Select item 3239000	NM_138690.3(GRIN3B):c.2210C>A (p.Pro737His)	GRIN3B (P737H)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3102557	NM_138690.3(GRIN3B):c.983C>T (p.Pro328Leu)	GRIN3B (P328L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102556	NM_138690.3(GRIN3B):c.905G>A (p.Arg302Gln)	GRIN3B (R302Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102555	NM_138690.3(GRIN3B):c.866T>G (p.Leu289Arg)	GRIN3B (L289R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102554	NM_138690.3(GRIN3B):c.671C>G (p.Ala224Gly)	GRIN3B (A224G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102553	NM_138690.3(GRIN3B):c.662C>T (p.Pro221Leu)	GRIN3B (P221L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102552	NM_138690.3(GRIN3B):c.619C>T (p.Arg207Trp)	GRIN3B (R207W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102551	NM_138690.3(GRIN3B):c.439C>G (p.Leu147Val)	GRIN3B (L147V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102550	NM_138690.3(GRIN3B):c.341T>C (p.Leu114Pro)	GRIN3B (L114P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102549	NM_138690.3(GRIN3B):c.3082G>A (p.Ala1028Thr)	GRIN3B (A1028T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102548	NM_138690.3(GRIN3B):c.3062G>A (p.Arg1021His)	GRIN3B (R1021H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102547	NM_138690.3(GRIN3B):c.2855C>G (p.Ala952Gly)	GRIN3B (A952G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102546	NM_138690.3(GRIN3B):c.2777G>A (p.Arg926Gln)	GRIN3B (R926Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102545	NM_138690.3(GRIN3B):c.2767C>G (p.Arg923Gly)	GRIN3B (R923G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102544	NM_138690.3(GRIN3B):c.2714T>A (p.Val905Glu)	GRIN3B (V905E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102543	NM_138690.3(GRIN3B):c.2689G>C (p.Glu897Gln)	GRIN3B (E897Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102542	NM_138690.3(GRIN3B):c.2658G>T (p.Glu886Asp)	GRIN3B (E886D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102541	NM_138690.3(GRIN3B):c.2594A>C (p.Lys865Thr)	GRIN3B (K865T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102539	NM_138690.3(GRIN3B):c.2365G>A (p.Glu789Lys)	GRIN3B (E789K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102538	NM_138690.3(GRIN3B):c.2195T>G (p.Leu732Arg)	GRIN3B (L732R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102537	NM_138690.3(GRIN3B):c.212G>T (p.Ser71Ile)	GRIN3B (S71I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102536	NM_138690.3(GRIN3B):c.2058C>A (p.His686Gln)	GRIN3B (H686Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102535	NM_138690.3(GRIN3B):c.1678C>T (p.Arg560Trp)	GRIN3B (R560W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102534	NM_138690.3(GRIN3B):c.164C>T (p.Ala55Val)	GRIN3B (A55V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102533	NM_138690.3(GRIN3B):c.1636A>G (p.Ser546Gly)	GRIN3B (S546G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102532	NM_138690.3(GRIN3B):c.1483T>C (p.Phe495Leu)	GRIN3B (F495L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102531	NM_138690.3(GRIN3B):c.1457G>A (p.Arg486Gln)	GRIN3B (R486Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102530	NM_138690.3(GRIN3B):c.1174G>A (p.Gly392Ser)	GRIN3B (G392S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3062384	GRCh37/hg19 19p13.3(chr19:260911-1210337)x1	ABCA7, ARHGAP45 +37 more	Copy number loss	not specified	GPathogenic
Select item 3062378	GRCh37/hg19 19p13.3(chr19:352288-1186507)x3	ABCA7, ARHGAP45 +34 more	Copy number gain	not specified	GUncertain significance
Select item 2689167	NM_138690.3(GRIN3B):c.1019G>A (p.Arg340Gln)	GRIN3B (R340Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2684882	GRCh37/hg19 19p13.3-13.2(chr19:260912-7246777)x3	MBD3L3, MBD3L4 +202 more	Copy number gain	not provided	GPathogenic
Select item 2648884	NM_138690.3(GRIN3B):c.2913C>T (p.Ala971=)	GRIN3B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2648883	NM_138690.3(GRIN3B):c.240C>A (p.Pro80=)	GRIN3B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2617171	NM_138690.3(GRIN3B):c.1705T>C (p.Phe569Leu)	GRIN3B (F569L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616116	NM_138690.3(GRIN3B):c.2165C>T (p.Ala722Val)	GRIN3B (A722V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598310	NM_138690.3(GRIN3B):c.980A>C (p.Gln327Pro)	GRIN3B (Q327P)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2596606	NM_138690.3(GRIN3B):c.2903G>A (p.Arg968His)	GRIN3B (R968H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596077	NM_138690.3(GRIN3B):c.176G>A (p.Arg59Gln)	GRIN3B (R59Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559998	NM_138690.3(GRIN3B):c.1133G>A (p.Arg378Gln)	GRIN3B (R378Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552764	NM_138690.3(GRIN3B):c.2759G>A (p.Gly920Asp)	GRIN3B (G920D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550840	NM_138690.3(GRIN3B):c.2449G>A (p.Val817Ile)	GRIN3B (V817I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539507	NM_138690.3(GRIN3B):c.1693C>A (p.Pro565Thr)	GRIN3B (P565T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536059	NM_138690.3(GRIN3B):c.1922C>T (p.Thr641Met)	GRIN3B (T641M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527675	NM_138690.3(GRIN3B):c.730C>T (p.Arg244Cys)	GRIN3B (R244C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525266	NM_138690.3(GRIN3B):c.1672C>T (p.Arg558Trp)	GRIN3B (R558W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512303	NM_138690.3(GRIN3B):c.1571G>A (p.Arg524Gln)	GRIN3B (R524Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494542	NM_138690.3(GRIN3B):c.2089G>C (p.Val697Leu)	GRIN3B (V697L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493264	NM_138690.3(GRIN3B):c.1699G>C (p.Gly567Arg)	GRIN3B (G567R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492747	NM_138690.3(GRIN3B):c.2599A>G (p.Ser867Gly)	GRIN3B (S867G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491325	NM_138690.3(GRIN3B):c.350A>T (p.His117Leu)	GRIN3B (H117L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487648	NM_138690.3(GRIN3B):c.1172A>C (p.Asp391Ala)	GRIN3B (D391A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482698	NM_138690.3(GRIN3B):c.826C>T (p.Pro276Ser)	GRIN3B (P276S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480816	NM_138690.3(GRIN3B):c.520G>C (p.Val174Leu)	GRIN3B (V174L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479546	NM_138690.3(GRIN3B):c.2434C>T (p.Pro812Ser)	GRIN3B (P812S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470458	NM_138690.3(GRIN3B):c.253G>A (p.Ala85Thr)	GRIN3B (A85T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467229	NM_138690.3(GRIN3B):c.1576C>T (p.His526Tyr)	GRIN3B (H526Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463288	NM_138690.3(GRIN3B):c.1613G>A (p.Arg538His)	GRIN3B (R538H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463198	NM_138690.3(GRIN3B):c.1828C>T (p.Arg610Cys)	GRIN3B (R610C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457093	NM_138690.3(GRIN3B):c.2776C>T (p.Arg926Trp)	GRIN3B (R926W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2425228	NC_000019.9:g.(?_589946)_(5696788_?)dup	ABCA7, ABHD17A +151 more	Duplication	not provided	GUncertain significance
Select item 2424336	NC_000019.9:g.(?_589946)_(2151333_?)dup	NDUFS7, ONECUT3 +61 more	Duplication	Cyclical neutropenia +1 more	GUncertain significance
Select item 2423454	NC_000019.9:g.(?_589946)_(4818389_?)dup	ABCA7, ABHD17A +138 more	Duplication	not provided	GUncertain significance
Select item 2408693	NM_138690.3(GRIN3B):c.970G>A (p.Gly324Arg)	GRIN3B (G324R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408482	NM_138690.3(GRIN3B):c.2757G>C (p.Glu919Asp)	GRIN3B (E919D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407967	NM_138690.3(GRIN3B):c.671C>T (p.Ala224Val)	GRIN3B (A224V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397521	NM_138690.3(GRIN3B):c.935C>T (p.Pro312Leu)	GRIN3B (P312L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395850	NM_138690.3(GRIN3B):c.1343C>G (p.Pro448Arg)	GRIN3B (P448R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394187	NM_138690.3(GRIN3B):c.794C>T (p.Pro265Leu)	GRIN3B (P265L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390109	NM_138690.3(GRIN3B):c.1679G>A (p.Arg560Gln)	GRIN3B (R560Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389519	NM_138690.3(GRIN3B):c.2749G>A (p.Ala917Thr)	GRIN3B (A917T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383434	NM_138690.3(GRIN3B):c.988G>C (p.Gly330Arg)	GRIN3B (G330R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369504	NM_138690.3(GRIN3B):c.1303G>A (p.Glu435Lys)	GRIN3B (E435K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368091	NM_138690.3(GRIN3B):c.1168C>T (p.Arg390Trp)	GRIN3B (R390W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363903	NM_138690.3(GRIN3B):c.1006C>T (p.Arg336Cys)	GRIN3B (R336C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357612	NM_138690.3(GRIN3B):c.1502G>A (p.Gly501Asp)	GRIN3B (G501D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350052	NM_138690.3(GRIN3B):c.88C>G (p.Leu30Val)	GRIN3B (L30V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349524	NM_138690.3(GRIN3B):c.130C>T (p.Pro44Ser)	GRIN3B (P44S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346508	NM_138690.3(GRIN3B):c.668C>T (p.Ala223Val)	GRIN3B (A223V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338381	NM_138690.3(GRIN3B):c.2182G>A (p.Gly728Ser)	GRIN3B (G728S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337447	NM_138690.3(GRIN3B):c.3119G>A (p.Gly1040Glu)	GRIN3B (G1040E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335894	NM_138690.3(GRIN3B):c.1036T>A (p.Ser346Thr)	GRIN3B (S346T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334211	NM_138690.3(GRIN3B):c.1018C>T (p.Arg340Trp)	GRIN3B (R340W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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