ClinVar for Gene (Select 10985) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3099090	NM_006836.2(GCN1):c.994T>C (p.Ser332Pro)	GCN1 (S332P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099089	NM_006836.2(GCN1):c.937C>T (p.Arg313Cys)	GCN1 (R313C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099088	NM_006836.2(GCN1):c.7979A>T (p.Asp2660Val)	GCN1 (D2660V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099087	NM_006836.2(GCN1):c.7946G>A (p.Arg2649Gln)	GCN1 (R2649Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099086	NM_006836.2(GCN1):c.793A>G (p.Thr265Ala)	GCN1 (T265A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099085	NM_006836.2(GCN1):c.7837G>A (p.Asp2613Asn)	GCN1 (D2613N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099084	NM_006836.2(GCN1):c.7643C>T (p.Pro2548Leu)	GCN1 (P2548L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099082	NM_006836.2(GCN1):c.754T>A (p.Tyr252Asn)	GCN1 (Y252N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099081	NM_006836.2(GCN1):c.752G>A (p.Arg251Gln)	GCN1 (R251Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099080	NM_006836.2(GCN1):c.7471G>A (p.Val2491Met)	GCN1 (V2491M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099079	NM_006836.2(GCN1):c.7169A>G (p.Asn2390Ser)	GCN1 (N2390S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099078	NM_006836.2(GCN1):c.710A>G (p.Lys237Arg)	GCN1 (K237R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099077	NM_006836.2(GCN1):c.7082G>T (p.Arg2361Leu)	GCN1 (R2361L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099076	NM_006836.2(GCN1):c.6633G>C (p.Glu2211Asp)	GCN1 (E2211D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099075	NM_006836.2(GCN1):c.6589C>G (p.Leu2197Val)	GCN1 (L2197V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099074	NM_006836.2(GCN1):c.5767C>A (p.Leu1923Ile)	GCN1 (L1923I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099073	NM_006836.2(GCN1):c.5749C>T (p.Arg1917Cys)	GCN1 (R1917C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099072	NM_006836.2(GCN1):c.5731G>A (p.Val1911Ile)	GCN1 (V1911I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099071	NM_006836.2(GCN1):c.5251C>T (p.His1751Tyr)	GCN1 (H1751Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099070	NM_006836.2(GCN1):c.5106G>C (p.Glu1702Asp)	GCN1 (E1702D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099069	NM_006836.2(GCN1):c.4940A>G (p.Asp1647Gly)	GCN1 (D1647G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099068	NM_006836.2(GCN1):c.4900A>T (p.Met1634Leu)	GCN1 (M1634L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099067	NM_006836.2(GCN1):c.4669G>T (p.Ala1557Ser)	GCN1 (A1557S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099065	NM_006836.2(GCN1):c.409G>C (p.Asp137His)	GCN1 (D137H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099064	NM_006836.2(GCN1):c.389C>G (p.Ser130Trp)	GCN1 (S130W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099063	NM_006836.2(GCN1):c.371T>C (p.Val124Ala)	GCN1 (V124A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099062	NM_006836.2(GCN1):c.3518C>T (p.Ala1173Val)	GCN1 (A1173V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099061	NM_006836.2(GCN1):c.3068C>G (p.Pro1023Arg)	GCN1 (P1023R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099060	NM_006836.2(GCN1):c.2980C>T (p.His994Tyr)	GCN1 (H994Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099059	NM_006836.2(GCN1):c.2510A>G (p.Gln837Arg)	GCN1 (Q837R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099058	NM_006836.2(GCN1):c.2278C>T (p.Arg760Trp)	GCN1 (R760W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099057	NM_006836.2(GCN1):c.2266C>T (p.Arg756Cys)	GCN1 (R756C)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3099056	NM_006836.2(GCN1):c.2210G>T (p.Arg737Leu)	GCN1 (R737L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099055	NM_006836.2(GCN1):c.2210G>A (p.Arg737Gln)	GCN1 (R737Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099054	NM_006836.2(GCN1):c.2098G>A (p.Ala700Thr)	GCN1 (A700T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099053	NM_006836.2(GCN1):c.1846A>C (p.Lys616Gln)	GCN1 (K616Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099052	NM_006836.2(GCN1):c.1746G>T (p.Arg582Ser)	GCN1 (R582S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099051	NM_006836.2(GCN1):c.1597A>G (p.Met533Val)	GCN1 (M533V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099050	NM_006836.2(GCN1):c.1495T>G (p.Leu499Val)	GCN1 (L499V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099048	NM_006836.2(GCN1):c.1321G>T (p.Ala441Ser)	GCN1 (A441S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2672525	NM_006836.2(GCN1):c.6046G>T (p.Asp2016Tyr)	GCN1 (D2016Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2643395	NM_006836.2(GCN1):c.4893G>A (p.Thr1631=)	GCN1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2643394	NM_006836.2(GCN1):c.7653T>C (p.Leu2551=)	GCN1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2622329	NM_006836.2(GCN1):c.7567C>T (p.Pro2523Ser)	GCN1 (P2523S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613301	NM_006836.2(GCN1):c.5419A>G (p.Met1807Val)	GCN1 (M1807V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610760	NM_006836.2(GCN1):c.4108A>G (p.Ile1370Val)	GCN1 (I1370V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610171	NM_006836.2(GCN1):c.3635C>T (p.Pro1212Leu)	GCN1 (P1212L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2609021	NM_006836.2(GCN1):c.4124G>C (p.Gly1375Ala)	GCN1 (G1375A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589779	NM_006836.2(GCN1):c.1509C>G (p.Asp503Glu)	GCN1 (D503E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2568849	NM_006836.2(GCN1):c.6971C>T (p.Ala2324Val)	GCN1 (A2324V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551494	NM_006836.2(GCN1):c.2993A>G (p.Glu998Gly)	GCN1 (E998G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551229	NM_006836.2(GCN1):c.2912C>T (p.Ala971Val)	GCN1 (A971V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550315	NM_006836.2(GCN1):c.2684C>G (p.Pro895Arg)	GCN1 (P895R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550277	NM_006836.2(GCN1):c.3169G>A (p.Val1057Ile)	GCN1 (V1057I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549814	NM_006836.2(GCN1):c.1025T>A (p.Leu342Gln)	GCN1 (L342Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544447	NM_006836.2(GCN1):c.4297C>T (p.Arg1433Cys)	GCN1 (R1433C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538284	NM_006836.2(GCN1):c.4252A>C (p.Met1418Leu)	GCN1 (M1418L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536959	NM_006836.2(GCN1):c.3118A>T (p.Met1040Leu)	GCN1 (M1040L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535334	NM_006836.2(GCN1):c.1354G>A (p.Ala452Thr)	GCN1 (A452T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535160	NM_006836.2(GCN1):c.698T>G (p.Met233Arg)	GCN1 (M233R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532926	NM_006836.2(GCN1):c.4529C>T (p.Ser1510Leu)	GCN1 (S1510L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529807	NM_006836.2(GCN1):c.7508G>A (p.Gly2503Asp)	GCN1 (G2503D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528625	NM_006836.2(GCN1):c.7976C>T (p.Ala2659Val)	GCN1 (A2659V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522215	NM_006836.2(GCN1):c.5986C>T (p.Arg1996Trp)	GCN1 (R1996W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514118	NM_006836.2(GCN1):c.1105G>A (p.Val369Ile)	GCN1 (V369I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509604	NM_006836.2(GCN1):c.7853A>G (p.Asn2618Ser)	GCN1 (N2618S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495080	NM_006836.2(GCN1):c.7802C>T (p.Thr2601Ile)	GCN1 (T2601I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486362	NM_006836.2(GCN1):c.4427G>T (p.Arg1476Leu)	GCN1 (R1476L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486327	NM_006836.2(GCN1):c.1819G>A (p.Glu607Lys)	GCN1 (E607K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474446	NM_006836.2(GCN1):c.337G>A (p.Ala113Thr)	GCN1 (A113T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461440	NM_006836.2(GCN1):c.1669C>T (p.Leu557Phe)	GCN1 (L557F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457237	NM_006836.2(GCN1):c.7507G>A (p.Gly2503Ser)	GCN1 (G2503S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409454	NM_006836.2(GCN1):c.7866G>A (p.Met2622Ile)	GCN1 (M2622I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404110	NM_006836.2(GCN1):c.1642A>G (p.Arg548Gly)	GCN1 (R548G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382744	NM_006836.2(GCN1):c.712C>T (p.Pro238Ser)	GCN1 (P238S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374451	NM_006836.2(GCN1):c.1759A>G (p.Thr587Ala)	GCN1 (T587A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369334	NM_006836.2(GCN1):c.1108A>G (p.Ser370Gly)	GCN1 (S370G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361561	NM_006836.2(GCN1):c.4483G>T (p.Val1495Leu)	GCN1 (V1495L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356321	NM_006836.2(GCN1):c.2573C>T (p.Ala858Val)	GCN1 (A858V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355160	NM_006836.2(GCN1):c.3565C>T (p.Arg1189Cys)	GCN1 (R1189C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353339	NM_006836.2(GCN1):c.484G>A (p.Val162Met)	GCN1 (V162M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349578	NM_006836.2(GCN1):c.6274C>T (p.Arg2092Trp)	GCN1 (R2092W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347807	NM_006836.2(GCN1):c.3541G>A (p.Glu1181Lys)	GCN1 (E1181K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344998	NM_006836.2(GCN1):c.1373C>T (p.Thr458Met)	GCN1 (T458M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343589	NM_006836.2(GCN1):c.509C>T (p.Thr170Met)	GCN1 (T170M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342320	NM_006836.2(GCN1):c.2969C>T (p.Thr990Met)	GCN1 (T990M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339308	NM_006836.2(GCN1):c.3593T>C (p.Met1198Thr)	GCN1 (M1198T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335984	NM_006836.2(GCN1):c.1003A>G (p.Met335Val)	GCN1 (M335V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334981	NM_006836.2(GCN1):c.7556C>T (p.Ala2519Val)	GCN1 (A2519V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331388	NM_006836.2(GCN1):c.1322C>T (p.Ala441Val)	GCN1 (A441V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2327129	NM_006836.2(GCN1):c.6907G>A (p.Val2303Met)	GCN1 (V2303M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326874	NM_006836.2(GCN1):c.5408G>A (p.Arg1803Gln)	GCN1 (R1803Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321490	NM_006836.2(GCN1):c.2212G>T (p.Val738Phe)	GCN1 (V738F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320136	NM_006836.2(GCN1):c.4585C>T (p.Pro1529Ser)	GCN1 (P1529S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317146	NM_006836.2(GCN1):c.6226G>A (p.Val2076Met)	GCN1 (V2076M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314503	NM_006836.2(GCN1):c.66T>G (p.Ser22Arg)	GCN1 (S22R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310134	NM_006836.2(GCN1):c.6523C>T (p.Leu2175Phe)	GCN1 (L2175F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309075	NM_006836.2(GCN1):c.3463G>C (p.Asp1155His)	GCN1 (D1155H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308831	NM_006836.2(GCN1):c.1469T>C (p.Val490Ala)	GCN1 (V490A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306295	NM_006836.2(GCN1):c.4256T>C (p.Met1419Thr)	GCN1 (M1419T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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