GRID1[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 148945	GRCh38/hg38 10q11.23-23.2(chr10:50729367-87147204)x3	LOC129390180, LOC129390181 +1008 more	Copy number gain	See cases	GPathogenic
Select item 153276	GRCh38/hg38 10q22.3-23.2(chr10:79689360-87223773)x1	ADIRF, ADIRF-AS1 +174 more	Copy number loss	See cases	GPathogenic
Select item 58748	GRCh38/hg38 10q22.3-23.2(chr10:79719429-87358394)x1	ADIRF, ADIRF-AS1 +178 more	Copy number loss	See cases	GPathogenic
Select item 147367	GRCh38/hg38 10q22.3-23.2(chr10:79802022-87068261)x1	ADIRF, ADIRF-AS1 +166 more	Copy number loss	See cases	GPathogenic
Select item 58751	GRCh38/hg38 10q22.3-23.2(chr10:79802022-87358394)x1	ADIRF, ADIRF-AS1 +178 more	Copy number loss	See cases	GPathogenic
Select item 155111	GRCh38/hg38 10q22.3-23.2(chr10:79881238-87180672)x1	FAM25A, GHITM +168 more	Copy number loss	See cases	GPathogenic
Select item 59702	GRCh38/hg38 10q22.3-23.2(chr10:79881238-87182117)x3	SHLD2, SNCG +168 more	Copy number gain	See cases	GPathogenic
Select item 33096	GRCh38/hg38 10q22.3-23.2(chr10:79882162-87068261)x1	ADIRF, ADIRF-AS1 +163 more	Copy number loss	See cases	GPathogenic
Select item 58757	GRCh38/hg38 10q22.3-23.2(chr10:79898516-87109827)x1	LOC130004227, LOC130004228 +168 more	Copy number loss	See cases	GPathogenic
Select item 58755	GRCh38/hg38 10q22.3-23.2(chr10:79898516-87358394)x1	ADIRF, ADIRF-AS1 +175 more	Copy number loss	See cases	GPathogenic
Select item 58754	GRCh38/hg38 10q22.3-23.2(chr10:79898516-86964367)x1	ANXA11, BMPR1A +150 more	Copy number loss	See cases	GPathogenic
Select item 146022	GRCh38/hg38 10q22.3-23.2(chr10:79925613-86951708)x1	LINC00857, LINC00858 +147 more	Copy number loss	See cases	GPathogenic
Select item 59703	GRCh38/hg38 10q23.1-23.31(chr10:84434981-89150802)x3	ATAD1, ACTA2 +151 more	Copy number gain	See cases	GPathogenic
Select item 2207898	NM_017551.3(GRID1):c.2984G>A (p.Gly995Asp)	GRID1, GRID1-AS1 (G995D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2502410	NM_017551.3(GRID1):c.2950C>T (p.Pro984Ser)	GRID1, GRID1-AS1 (P984S)	Single nucleotide variant (missense variant)	GRID1-associated neurodevelopmental disorder	GUncertain significance
Select item 2590488	NM_017551.3(GRID1):c.2939C>T (p.Pro980Leu)	GRID1, GRID1-AS1 (P980L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2502409	NM_017551.3(GRID1):c.2855C>T (p.Pro952Leu)	GRID1, GRID1-AS1 (P952L)	Single nucleotide variant (missense variant)	GRID1-associated neurodevelopmental disorder	GUncertain significance
Select item 2561444	NM_017551.3(GRID1):c.2753G>A (p.Arg918Gln)	GRID1, GRID1-AS1 (R918Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2502408	NM_017551.3(GRID1):c.2690C>T (p.Ser897Leu)	GRID1, GRID1-AS1 (S897L)	Single nucleotide variant (missense variant)	GRID1-associated neurodevelopmental disorder	GUncertain significance
Select item 3282697	NM_017551.3(GRID1):c.2666C>T (p.Ala889Val)	GRID1, GRID1-AS1 (A889V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2689160	NM_017551.3(GRID1):c.2636G>A (p.Arg879His)	GRID1, GRID1-AS1 (R879H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2308905	NM_017551.3(GRID1):c.2597A>G (p.Lys866Arg)	GRID1 (K866R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461367	NM_017551.3(GRID1):c.2591C>T (p.Thr864Ile)	GRID1 (T864I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366264	NM_017551.3(GRID1):c.2575C>T (p.Arg859Trp)	GRID1 (R859W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102339	NM_017551.3(GRID1):c.2530C>G (p.Leu844Val)	GRID1 (L844V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2502407	NM_017551.3(GRID1):c.2449G>A (p.Ala817Thr)	GRID1 (A817T)	Single nucleotide variant (missense variant)	GRID1-associated neurodevelopmental disorder	GUncertain significance
Select item 2340170	NM_017551.3(GRID1):c.2326C>T (p.His776Tyr)	GRID1 (H776Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102338	NM_017551.3(GRID1):c.2270C>T (p.Ser757Leu)	GRID1 (S757L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2502402	NM_017551.3(GRID1):c.2255C>T (p.Thr752Met)	GRID1 (T752M)	Single nucleotide variant (missense variant)	GRID1-associated neurodevelopmental disorder	GUncertain significance
Select item 3102337	NM_017551.3(GRID1):c.2152G>T (p.Ala718Ser)	GRID1 (A718S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410007	NM_017551.3(GRID1):c.2146G>A (p.Gly716Arg)	GRID1 (G716R)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2502406	NM_017551.3(GRID1):c.2120A>G (p.Glu707Gly)	GRID1 (E707G)	Single nucleotide variant (missense variant)	GRID1-associated neurodevelopmental disorder	GUncertain significance
Select item 3282702	NM_017551.3(GRID1):c.2075G>A (p.Arg692Gln)	GRID1 (R692Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621775	NM_017551.3(GRID1):c.2056G>A (p.Ala686Thr)	GRID1 (A686T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2502405	NM_017551.3(GRID1):c.2050G>C (p.Asp684His)	GRID1 (D684H)	Single nucleotide variant (missense variant)	GRID1-associated neurodevelopmental disorder	GUncertain significance
Select item 2502404	NM_017551.3(GRID1):c.1948G>A (p.Ala650Thr)	GRID1 (A650T)	Single nucleotide variant (missense variant)	GRID1-associated neurodevelopmental disorder	GPathogenic
Select item 2398275	NM_017551.3(GRID1):c.1911G>T (p.Trp637Cys)	GRID1 (W637C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597539	NM_017551.3(GRID1):c.1894A>C (p.Ile632Leu)	GRID1 (I632L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511681	NM_017551.3(GRID1):c.1891C>A (p.Arg631Ser)	GRID1 (R631S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211380	NM_017551.3(GRID1):c.1873G>A (p.Val625Met)	GRID1 (V625M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102336	NM_017551.3(GRID1):c.1849G>A (p.Val617Ile)	GRID1 (V617I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526416	NM_017551.3(GRID1):c.1819A>G (p.Ser607Gly)	GRID1 (S607G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2502403	NM_017551.3(GRID1):c.1811C>T (p.Thr604Ile)	GRID1 (T604I)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2395011	NM_017551.3(GRID1):c.1808C>T (p.Ala603Val)	GRID1 (A603V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385716	NM_017551.3(GRID1):c.1808C>A (p.Ala603Asp)	GRID1 (A603D)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3102335	NM_017551.3(GRID1):c.1801G>T (p.Ala601Ser)	GRID1 (A601S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282700	NM_017551.3(GRID1):c.1755G>C (p.Arg585Ser)	GRID1 (R585S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3355807	NM_017551.3(GRID1):c.1690G>C (p.Ala564Pro)	GRID1 (A564P)	Single nucleotide variant (missense variant)	GRID1-related disorder	GUncertain significance
Select item 2623876	NM_017551.3(GRID1):c.1660A>T (p.Ile554Phe)	GRID1 (I554F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309911	NM_017551.3(GRID1):c.1642C>T (p.Pro548Ser)	GRID1 (P548S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2232535	NM_017551.3(GRID1):c.1639A>G (p.Lys547Glu)	GRID1 (K547E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295122	NM_017551.3(GRID1):c.1625G>C (p.Gly542Ala)	GRID1 (G542A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1249619	NM_017551.3(GRID1):c.1585G>A (p.Val529Ile)	GRID1 (V529I)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2594317	NM_017551.3(GRID1):c.1513A>G (p.Ile505Val)	GRID1 (I505V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276933	NM_017551.3(GRID1):c.1496C>A (p.Thr499Asn)	GRID1 (T499N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102333	NM_017551.3(GRID1):c.1495A>G (p.Thr499Ala)	GRID1 (T499A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102332	NM_017551.3(GRID1):c.1477G>A (p.Gly493Ser)	GRID1 (G493S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492681	NM_017551.3(GRID1):c.1472G>C (p.Arg491Thr)	GRID1 (R491T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102331	NM_017551.3(GRID1):c.1409T>C (p.Val470Ala)	GRID1 (V470A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2502401	NM_017551.3(GRID1):c.1366A>C (p.Ile456Leu)	GRID1 (I456L)	Single nucleotide variant (missense variant)	GRID1-associated neurodevelopmental disorder	GUncertain significance
Select item 2502400	NM_017551.3(GRID1):c.1348G>A (p.Val450Met)	GRID1 (V450M)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2502399	NM_017551.3(GRID1):c.1339G>A (p.Glu447Lys)	GRID1 (E447K)	Single nucleotide variant (missense variant)	GRID1-associated neurodevelopmental disorder	GUncertain significance
Select item 1279125	NM_017551.3(GRID1):c.1288A>G (p.Met430Val)	GRID1 (M430V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3102330	NM_017551.3(GRID1):c.1286C>G (p.Pro429Arg)	GRID1 (P429R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2502398	NM_017551.3(GRID1):c.1285C>A (p.Pro429Thr)	GRID1 (P429T)	Single nucleotide variant (missense variant)	GRID1-associated neurodevelopmental disorder	GUncertain significance
Select item 2341592	NM_017551.3(GRID1):c.1151G>A (p.Arg384Gln)	GRID1 (R384Q)	Single nucleotide variant (missense variant)	GRID1-associated neurodevelopmental disorder +1 more	GUncertain significance
Select item 2502397	NM_017551.3(GRID1):c.1119C>A (p.His373Gln)	GRID1 (H373Q)	Single nucleotide variant (missense variant)	GRID1-associated neurodevelopmental disorder	GUncertain significance
Select item 2492746	NM_017551.3(GRID1):c.1088G>A (p.Arg363Lys)	GRID1 (R363K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102329	NM_017551.3(GRID1):c.1040C>G (p.Ala347Gly)	GRID1 (A347G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2502396	NM_017551.3(GRID1):c.1022G>A (p.Arg341Gln)	GRID1 (R341Q)	Single nucleotide variant (missense variant)	GRID1-associated neurodevelopmental disorder	GUncertain significance
Select item 2502395	NM_017551.3(GRID1):c.919G>A (p.Asp307Asn)	GRID1 (D307N)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2537821	NM_017551.3(GRID1):c.913C>T (p.Leu305Phe)	GRID1 (L305F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2502394	NM_017551.3(GRID1):c.899G>T (p.Arg300Leu)	GRID1 (R300L)	Single nucleotide variant (missense variant)	GRID1-associated neurodevelopmental disorder	GUncertain significance
Select item 3282701	NM_017551.3(GRID1):c.895C>G (p.His299Asp)	GRID1 (H299D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 219328	NM_017551.3(GRID1):c.884C>T (p.Thr295Met)	GRID1 (T295M)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 3102349	NM_017551.3(GRID1):c.883A>T (p.Thr295Ser)	GRID1 (T295S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541645	NM_017551.3(GRID1):c.868G>C (p.Asp290His)	GRID1 (D290H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102348	NM_017551.3(GRID1):c.860C>A (p.Ser287Tyr)	GRID1 (S287Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2502393	NM_017551.3(GRID1):c.857C>T (p.Pro286Leu)	GRID1 (P286L)	Single nucleotide variant (missense variant)	GRID1-associated neurodevelopmental disorder	GUncertain significance
Select item 2260749	NM_017551.3(GRID1):c.836C>T (p.Thr279Ile)	GRID1 (T279I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 146272	GRCh38/hg38 10q23.1-23.2(chr10:85937958-86195924)x3	GRID1, LOC130004223	Copy number gain	See cases	GLikely benign
Select item 2502392	NM_017551.3(GRID1):c.706G>T (p.Ala236Ser)	GRID1 (A236S)	Single nucleotide variant (missense variant)	GRID1-associated neurodevelopmental disorder	GUncertain significance
Select item 3102347	NM_017551.3(GRID1):c.679G>A (p.Ala227Thr)	GRID1 (A227T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265245	NM_017551.3(GRID1):c.673C>T (p.Arg225Cys)	GRID1 (R225C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389797	NM_017551.3(GRID1):c.662G>A (p.Arg221Gln)	GRID1 (R221Q)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2502391	NM_017551.3(GRID1):c.596A>G (p.Lys199Arg)	GRID1 (K199R)	Single nucleotide variant (missense variant)	GRID1-associated neurodevelopmental disorder	GUncertain significance
Select item 3102346	NM_017551.3(GRID1):c.574G>A (p.Val192Ile)	GRID1 (V192I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102345	NM_017551.3(GRID1):c.560G>A (p.Arg187Gln)	GRID1 (R187Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2622395	NM_017551.3(GRID1):c.523A>G (p.Ile175Val)	GRID1 (I175V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 157182	NM_017551.3(GRID1):c.520+7072_520+11519del	GRID1	Deletion (intron variant)	Gestational diabetes mellitus uncontrolled	Gnot provided
Select item 3102344	NM_017551.3(GRID1):c.514G>A (p.Glu172Lys)	GRID1 (E172K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102342	NM_017551.3(GRID1):c.508G>A (p.Asp170Asn)	GRID1 (D170N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2502390	NM_017551.3(GRID1):c.499A>G (p.Met167Val)	GRID1 (M167V)	Single nucleotide variant (missense variant)	GRID1-associated neurodevelopmental disorder	GUncertain significance
Select item 2502389	NM_017551.3(GRID1):c.496G>A (p.Val166Ile)	GRID1 (V166I)	Single nucleotide variant (missense variant)	GRID1-associated neurodevelopmental disorder	GUncertain significance
Select item 2408589	NM_017551.3(GRID1):c.482G>A (p.Arg161His)	GRID1 (R161H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2502388	NM_017551.3(GRID1):c.481C>T (p.Arg161Cys)	GRID1 (R161C)	Single nucleotide variant (missense variant)	GRID1-associated neurodevelopmental disorder	GUncertain significance
Select item 3102341	NM_017551.3(GRID1):c.449A>G (p.Asn150Ser)	GRID1 (N150S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 208923	NM_017551.3(GRID1):c.442C>T (p.Arg148Cys)	GRID1 (R148C)	Single nucleotide variant (missense variant)	Abnormality of neuronal migration	GBenign
Select item 208924	NM_017551.3(GRID1):c.437C>T (p.Pro146Leu)	GRID1 (P146L)	Single nucleotide variant (missense variant)	Abnormality of neuronal migration	GBenign
Select item 2502387	NM_017551.3(GRID1):c.407G>A (p.Gly136Asp)	GRID1 (G136D)	Single nucleotide variant (missense variant)	GRID1-associated neurodevelopmental disorder	GUncertain significance

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