ClinVar for Gene (Select 392862) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3102390	NM_001145118.2(GRID2IP):c.799G>A (p.Val267Met)	GRID2IP, LOC129997946 (V267M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102389	NM_001145118.2(GRID2IP):c.791C>T (p.Ser264Phe)	GRID2IP, LOC129997946 (S264F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102388	NM_001145118.2(GRID2IP):c.760C>A (p.Arg254Ser)	GRID2IP, LOC129997946 (R64S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102386	NM_001145118.2(GRID2IP):c.477C>G (p.Phe159Leu)	GRID2IP (F159L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102385	NM_001145118.2(GRID2IP):c.431T>G (p.Val144Gly)	GRID2IP (V144G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102384	NM_001145118.2(GRID2IP):c.3625C>G (p.Leu1209Val)	GRID2IP (L1026V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102383	NM_001145118.2(GRID2IP):c.3605G>T (p.Ser1202Ile)	GRID2IP (S1202I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102382	NM_001145118.2(GRID2IP):c.34G>A (p.Gly12Ser)	GRID2IP (G12S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102381	NM_001145118.2(GRID2IP):c.343C>G (p.Arg115Gly)	GRID2IP (R115G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102380	NM_001145118.2(GRID2IP):c.334G>C (p.Ala112Pro)	GRID2IP (A112P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102379	NM_001145118.2(GRID2IP):c.2650G>C (p.Glu884Gln)	GRID2IP (E701Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102378	NM_001145118.2(GRID2IP):c.2629G>T (p.Ala877Ser)	GRID2IP (A686S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102377	NM_001145118.2(GRID2IP):c.247C>T (p.Pro83Ser)	GRID2IP (P83S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102376	NM_001145118.2(GRID2IP):c.2348C>T (p.Ala783Val)	GRID2IP (A600V +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3102375	NM_001145118.2(GRID2IP):c.2228C>G (p.Ser743Cys)	GRID2IP (S552C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102374	NM_001145118.2(GRID2IP):c.2111A>T (p.Glu704Val)	GRID2IP (E513V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102372	NM_001145118.2(GRID2IP):c.2006C>T (p.Thr669Ile)	GRID2IP (T486I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102371	NM_001145118.2(GRID2IP):c.199C>T (p.Arg67Cys)	GRID2IP (R67C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102370	NM_001145118.2(GRID2IP):c.1990C>G (p.Arg664Gly)	GRID2IP (R473G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102369	NM_001145118.2(GRID2IP):c.1982C>T (p.Pro661Leu)	GRID2IP (P470L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102368	NM_001145118.2(GRID2IP):c.1951G>C (p.Asp651His)	GRID2IP (D460H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102367	NM_001145118.2(GRID2IP):c.1872C>A (p.Ser624Arg)	GRID2IP (S433R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102366	NM_001145118.2(GRID2IP):c.181A>T (p.Ser61Cys)	GRID2IP (S61C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102364	NM_001145118.2(GRID2IP):c.154G>A (p.Val52Met)	GRID2IP (V52M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102363	NM_001145118.2(GRID2IP):c.1412C>T (p.Thr471Met)	GRID2IP (T471M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102362	NM_001145118.2(GRID2IP):c.1288G>A (p.Val430Ile)	GRID2IP (V430I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3062958	GRCh37/hg19 7p22.1(chr7:6007649-6753402)x3	AIMP2, CYTH3 +14 more	Copy number gain	not specified	GUncertain significance
Select item 2684469	GRCh37/hg19 7p22.3-21.3(chr7:43361-8890475)x3	PSMG3, RAC1 +73 more	Copy number gain	not provided	GPathogenic
Select item 2657304	NM_001145118.2(GRID2IP):c.1449G>A (p.Leu483=)	GRID2IP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2657303	NM_001145118.2(GRID2IP):c.2115C>T (p.Asn705=)	GRID2IP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2657302	NM_001145118.2(GRID2IP):c.2271A>C (p.Pro757=)	GRID2IP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2657301	NM_001145118.2(GRID2IP):c.2832C>G (p.Ala944=)	GRID2IP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2657300	NM_001145118.2(GRID2IP):c.2961C>T (p.Ala987=)	GRID2IP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2657299	NM_001145118.2(GRID2IP):c.3363C>T (p.Ser1121=)	GRID2IP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2623196	NM_001145118.2(GRID2IP):c.2447G>C (p.Arg816Pro)	GRID2IP (R816P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615459	NM_001145118.2(GRID2IP):c.1514G>A (p.Arg505His)	GRID2IP (R314H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610961	NM_001145118.2(GRID2IP):c.2333G>A (p.Arg778Gln)	GRID2IP (R587Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608782	NM_001145118.2(GRID2IP):c.659G>C (p.Arg220Pro)	GRID2IP (R220P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595320	NM_001145118.2(GRID2IP):c.572T>G (p.Leu191Arg)	GRID2IP (L191R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594329	NM_001145118.2(GRID2IP):c.671C>T (p.Ala224Val)	GRID2IP (A41V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589224	NM_001145118.2(GRID2IP):c.1685G>A (p.Arg562Gln)	GRID2IP (R379Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558947	NM_001145118.2(GRID2IP):c.440T>G (p.Ile147Ser)	GRID2IP (I147S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549036	NM_001145118.2(GRID2IP):c.3036C>A (p.Asn1012Lys)	GRID2IP (N821K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547243	NM_001145118.2(GRID2IP):c.2084C>G (p.Thr695Ser)	GRID2IP (T504S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543515	NM_001145118.2(GRID2IP):c.2566G>A (p.Asp856Asn)	GRID2IP (D673N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540247	NM_001145118.2(GRID2IP):c.1979G>A (p.Arg660His)	GRID2IP (R477H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538422	NM_001145118.2(GRID2IP):c.1513C>T (p.Arg505Cys)	GRID2IP (R505C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538038	NM_001145118.2(GRID2IP):c.3542C>T (p.Ala1181Val)	GRID2IP (A990V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521794	NM_001145118.2(GRID2IP):c.2501G>A (p.Arg834Gln)	GRID2IP (R651Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520808	NM_001145118.2(GRID2IP):c.115C>A (p.His39Asn)	GRID2IP (H39N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519620	NM_001145118.2(GRID2IP):c.1226G>A (p.Arg409His)	GRID2IP (R219H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518396	NM_001145118.2(GRID2IP):c.2402C>T (p.Pro801Leu)	GRID2IP (P610L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516904	NM_001145118.2(GRID2IP):c.2446C>T (p.Arg816Trp)	GRID2IP (R633W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516024	NM_001145118.2(GRID2IP):c.2804C>G (p.Ala935Gly)	GRID2IP (A752G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515971	NM_001145118.2(GRID2IP):c.1145C>T (p.Ala382Val)	GRID2IP (A192V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512686	NM_001145118.2(GRID2IP):c.50T>C (p.Phe17Ser)	GRID2IP (F17S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512034	NM_001145118.2(GRID2IP):c.1967C>T (p.Pro656Leu)	GRID2IP (P465L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490232	NM_001145118.2(GRID2IP):c.2342C>G (p.Ala781Gly)	GRID2IP (A598G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490141	NM_001145118.2(GRID2IP):c.1885C>A (p.Pro629Thr)	GRID2IP (P629T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489882	NM_001145118.2(GRID2IP):c.2756A>G (p.Gln919Arg)	GRID2IP (Q736R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488037	NM_001145118.2(GRID2IP):c.3203C>G (p.Ala1068Gly)	GRID2IP (A1068G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487955	NM_001145118.2(GRID2IP):c.3551T>A (p.Met1184Lys)	GRID2IP (M1001K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483923	NM_001145118.2(GRID2IP):c.1603C>T (p.Arg535Cys)	GRID2IP (R344C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483383	NM_001145118.2(GRID2IP):c.2434C>T (p.Pro812Ser)	GRID2IP (P629S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466470	NM_001145118.2(GRID2IP):c.1249G>A (p.Glu417Lys)	GRID2IP (E227K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465138	NM_001145118.2(GRID2IP):c.1481G>A (p.Arg494Gln)	GRID2IP (R303Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463569	NM_001145118.2(GRID2IP):c.815G>A (p.Gly272Asp)	GRID2IP, LOC129997946 (G272D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458665	NM_001145118.2(GRID2IP):c.2419G>A (p.Val807Met)	GRID2IP (V624M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410196	NM_001145118.2(GRID2IP):c.2799T>A (p.His933Gln)	GRID2IP (H742Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399545	NM_001145118.2(GRID2IP):c.184C>T (p.Arg62Cys)	GRID2IP (R62C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399108	NM_001145118.2(GRID2IP):c.946A>C (p.Lys316Gln)	GRID2IP (K126Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398121	NM_001145118.2(GRID2IP):c.694C>G (p.Arg232Gly)	GRID2IP, LOC129997946 (R232G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397068	NM_001145118.2(GRID2IP):c.1667A>C (p.Tyr556Ser)	GRID2IP (Y365S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396753	NM_001145118.2(GRID2IP):c.1069G>A (p.Val357Ile)	GRID2IP (V167I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391003	NM_001145118.2(GRID2IP):c.1543G>A (p.Gly515Ser)	GRID2IP (G332S +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2387948	NM_001145118.2(GRID2IP):c.739C>T (p.Arg247Cys)	GRID2IP, LOC129997946 (R64C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387725	NM_001145118.2(GRID2IP):c.2017C>T (p.Pro673Ser)	GRID2IP (P490S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383575	NM_001145118.2(GRID2IP):c.2138A>G (p.His713Arg)	GRID2IP (H713R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382427	NM_001145118.2(GRID2IP):c.170T>G (p.Val57Gly)	GRID2IP (V57G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374644	NM_001145118.2(GRID2IP):c.1361A>G (p.Tyr454Cys)	GRID2IP (Y454C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363713	NM_001145118.2(GRID2IP):c.2252C>G (p.Pro751Arg)	GRID2IP (P751R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358191	NM_001145118.2(GRID2IP):c.359T>C (p.Leu120Pro)	GRID2IP (L120P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354771	NM_001145118.2(GRID2IP):c.1807G>A (p.Glu603Lys)	GRID2IP (E420K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353661	NM_001145118.2(GRID2IP):c.3532G>A (p.Gly1178Ser)	GRID2IP (G995S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352703	NM_001145118.2(GRID2IP):c.3442G>C (p.Gly1148Arg)	GRID2IP (G957R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350415	NM_001145118.2(GRID2IP):c.1393G>A (p.Ala465Thr)	GRID2IP (A465T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348216	NM_001145118.2(GRID2IP):c.372G>C (p.Lys124Asn)	GRID2IP (K124N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345768	NM_001145118.2(GRID2IP):c.478G>A (p.Ala160Thr)	GRID2IP (A160T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339886	NM_001145118.2(GRID2IP):c.2198G>A (p.Ser733Asn)	GRID2IP (S542N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328616	NM_001145118.2(GRID2IP):c.1894A>G (p.Ser632Gly)	GRID2IP (S449G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312674	NM_001145118.2(GRID2IP):c.1644C>A (p.Asn548Lys)	GRID2IP (N357K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312288	NM_001145118.2(GRID2IP):c.85G>C (p.Val29Leu)	GRID2IP (V29L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308795	NM_001145118.2(GRID2IP):c.48C>G (p.Asp16Glu)	GRID2IP (D16E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297520	NM_001145118.2(GRID2IP):c.2242C>A (p.His748Asn)	GRID2IP (H557N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287282	NM_001145118.2(GRID2IP):c.377C>G (p.Pro126Arg)	GRID2IP (P126R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2282410	NM_001145118.2(GRID2IP):c.1942A>C (p.Ile648Leu)	GRID2IP (I465L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278155	NM_001145118.2(GRID2IP):c.367C>G (p.Arg123Gly)	GRID2IP (R123G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277362	NM_001145118.2(GRID2IP):c.1525T>C (p.Ser509Pro)	GRID2IP (S318P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271972	NM_001145118.2(GRID2IP):c.814G>C (p.Gly272Arg)	GRID2IP, LOC129997946 (G82R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271586	NM_001145118.2(GRID2IP):c.191G>A (p.Arg64His)	GRID2IP (R64H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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