"Ambry Genetics"[submitter] AND "IGL"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3332136	NM_007128.4(VPREB1):c.13C>G (p.Pro5Ala)	IGL, VPREB1 (P5A)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 3188735	NM_007128.4(VPREB1):c.67C>G (p.Leu23Val)	IGL, VPREB1 (L23V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332135	NM_007128.4(VPREB1):c.80C>T (p.Pro27Leu)	IGL, VPREB1 (P26L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188731	NM_007128.4(VPREB1):c.160G>A (p.Val54Ile)	IGL, VPREB1 (V54I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2531931	NM_007128.4(VPREB1):c.253C>T (p.Pro85Ser)	IGL, VPREB1 (P85S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358037	NM_007128.4(VPREB1):c.274G>A (p.Asp92Asn)	IGL, VPREB1 (D91N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205029	NM_007128.4(VPREB1):c.296A>T (p.Tyr99Phe)	IGL, VPREB1 (Y99F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188732	NM_007128.4(VPREB1):c.305T>A (p.Ile102Asn)	IGL, VPREB1 (I102N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188733	NM_007128.4(VPREB1):c.355G>T (p.Ala119Ser)	IGL, VPREB1 (A118S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470483	NM_007128.4(VPREB1):c.367G>C (p.Glu123Gln)	IGL, VPREB1 (E123Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188734	NM_007128.4(VPREB1):c.388G>C (p.Glu130Gln)	IGL, VPREB1 (E130Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379134	NM_007128.4(VPREB1):c.427C>T (p.Arg143Cys)	IGL, VPREB1 (R142C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372282	NM_080764.4(ZNF280B):c.1564G>C (p.Val522Leu)	IGL, ZNF280B (V522L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2381056	NM_080764.4(ZNF280B):c.1396C>T (p.Arg466Trp)	IGL, ZNF280B (R466W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194863	NM_080764.4(ZNF280B):c.1345T>A (p.Cys449Ser)	IGL, ZNF280B (C449S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2331279	NM_080764.4(ZNF280B):c.1333A>G (p.Thr445Ala)	IGL, ZNF280B (T445A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2410594	NM_080764.4(ZNF280B):c.1192C>A (p.Pro398Thr)	IGL, ZNF280B (P398T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335355	NM_080764.4(ZNF280B):c.1086C>T (p.Ile362=)	IGL, ZNF280B	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 3194861	NM_080764.4(ZNF280B):c.1031C>G (p.Thr344Ser)	IGL, ZNF280B (T344S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2518718	NM_080764.4(ZNF280B):c.1021A>G (p.Asn341Asp)	IGL, ZNF280B (N341D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2462514	NM_080764.4(ZNF280B):c.888A>T (p.Glu296Asp)	IGL, ZNF280B (E296D)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2267468	NM_080764.4(ZNF280B):c.754A>G (p.Asn252Asp)	IGL, ZNF280B (N252D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2242458	NM_080764.4(ZNF280B):c.706C>T (p.Pro236Ser)	IGL, ZNF280B (P236S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335354	NM_080764.4(ZNF280B):c.648T>A (p.Ser216Arg)	IGL, ZNF280B (S216R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2412018	NM_080764.4(ZNF280B):c.535G>A (p.Glu179Lys)	IGL, ZNF280B (E179K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2345340	NM_080764.4(ZNF280B):c.533T>C (p.Phe178Ser)	IGL, ZNF280B (F178S)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3335353	NM_080764.4(ZNF280B):c.500A>G (p.Glu167Gly)	IGL, ZNF280B (E167G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2258333	NM_080764.4(ZNF280B):c.470G>A (p.Ser157Asn)	IGL, ZNF280B (S157N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2397943	NM_080764.4(ZNF280B):c.440C>T (p.Thr147Ile)	IGL, ZNF280B (T147I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2535607	NM_080764.4(ZNF280B):c.406A>G (p.Asn136Asp)	IGL, ZNF280B (N136D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194864	NM_080764.4(ZNF280B):c.310G>T (p.Ala104Ser)	IGL, ZNF280B (A104S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2557319	NM_080764.4(ZNF280B):c.290A>G (p.Glu97Gly)	IGL, ZNF280B (E97G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194862	NM_080764.4(ZNF280B):c.110A>G (p.His37Arg)	IGL, ZNF280B (H37R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194865	NM_080764.4(ZNF280B):c.68T>C (p.Val23Ala)	IGL, ZNF280B (V23A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2343174	NM_080740.5(ZNF280A):c.1577C>T (p.Thr526Met)	IGL, ZNF280A (T526M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2236455	NM_080740.5(ZNF280A):c.1556C>T (p.Pro519Leu)	IGL, ZNF280A (P519L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495392	NM_080740.5(ZNF280A):c.1553C>G (p.Ser518Cys)	IGL, ZNF280A (S518C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535095	NM_080740.5(ZNF280A):c.1544C>T (p.Pro515Leu)	IGL, ZNF280A (P515L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393492	NM_080740.5(ZNF280A):c.1540G>T (p.Asp514Tyr)	IGL, ZNF280A (D514Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318078	NM_080740.5(ZNF280A):c.1513A>T (p.Met505Leu)	IGL, ZNF280A (M505L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334846	NM_080740.5(ZNF280A):c.1492G>C (p.Val498Leu)	IGL, ZNF280A (V498L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194854	NM_080740.5(ZNF280A):c.1376A>G (p.Gln459Arg)	IGL, ZNF280A (Q459R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335351	NM_080740.5(ZNF280A):c.1295T>C (p.Phe432Ser)	IGL, ZNF280A (F432S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194853	NM_080740.5(ZNF280A):c.1219G>A (p.Ala407Thr)	IGL, ZNF280A (A407T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464799	NM_080740.5(ZNF280A):c.1211C>T (p.Ser404Leu)	IGL, ZNF280A (S404L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411536	NM_080740.5(ZNF280A):c.1177C>G (p.Pro393Ala)	IGL, ZNF280A (P393A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460160	NM_080740.5(ZNF280A):c.1132G>A (p.Val378Ile)	IGL, ZNF280A (V378I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194851	NM_080740.5(ZNF280A):c.1093G>C (p.Val365Leu)	IGL, ZNF280A (V365L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194850	NM_080740.5(ZNF280A):c.1078A>G (p.Met360Val)	IGL, ZNF280A (M360V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194849	NM_080740.5(ZNF280A):c.1021C>T (p.Arg341Trp)	IGL, ZNF280A (R341W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208695	NM_080740.5(ZNF280A):c.1016G>A (p.Cys339Tyr)	IGL, ZNF280A (C339Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2565307	NM_080740.5(ZNF280A):c.1011G>C (p.Gln337His)	IGL, ZNF280A (Q337H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194860	NM_080740.5(ZNF280A):c.982G>A (p.Asp328Asn)	IGL, ZNF280A (D328N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335352	NM_080740.5(ZNF280A):c.916G>A (p.Val306Ile)	IGL, ZNF280A (V306I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219196	NM_080740.5(ZNF280A):c.869C>T (p.Pro290Leu)	IGL, ZNF280A (P290L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207924	NM_080740.5(ZNF280A):c.851A>G (p.His284Arg)	IGL, ZNF280A (H284R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194859	NM_080740.5(ZNF280A):c.746C>T (p.Ala249Val)	IGL, ZNF280A (A249V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194858	NM_080740.5(ZNF280A):c.715C>T (p.Leu239Phe)	IGL, ZNF280A (L239F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358294	NM_080740.5(ZNF280A):c.692C>G (p.Ala231Gly)	IGL, ZNF280A (A231G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461322	NM_080740.5(ZNF280A):c.685C>T (p.Pro229Ser)	IGL, ZNF280A (P229S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397306	NM_080740.5(ZNF280A):c.566G>T (p.Gly189Val)	IGL, ZNF280A (G189V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396988	NM_080740.5(ZNF280A):c.347C>A (p.Thr116Asn)	IGL, ZNF280A (T116N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382880	NM_080740.5(ZNF280A):c.298A>C (p.Ile100Leu)	IGL, ZNF280A (I100L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516233	NM_080740.5(ZNF280A):c.251C>T (p.Ala84Val)	IGL, ZNF280A (A84V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194857	NM_080740.5(ZNF280A):c.238C>T (p.Arg80Cys)	IGL, ZNF280A (R80C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194856	NM_080740.5(ZNF280A):c.181A>C (p.Asn61His)	IGL, ZNF280A (N61H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290468	NM_080740.5(ZNF280A):c.127G>A (p.Asp43Asn)	IGL, ZNF280A (D43N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335350	NM_080740.5(ZNF280A):c.46A>C (p.Asn16His)	IGL, ZNF280A (N16H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321373	NM_206956.3(PRAME):c.1513T>C (p.Cys505Arg)	IGL, PRAME (C489R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591552	NM_206956.3(PRAME):c.1510C>T (p.Pro504Ser)	IGL, PRAME (P504S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218126	NM_206956.3(PRAME):c.1465C>T (p.His489Tyr)	IGL, PRAME (H489Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218125	NM_206956.3(PRAME):c.1426C>T (p.Arg476Trp)	IGL, PRAME (R460W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394902	NM_206956.3(PRAME):c.1408T>G (p.Leu470Val)	IGL, PRAME (L470V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220089	NM_206956.3(PRAME):c.1377G>T (p.Arg459Ser)	IGL, PRAME (R443S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535753	NM_206956.3(PRAME):c.1361C>G (p.Thr454Ser)	IGL, PRAME (T454S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218124	NM_206956.3(PRAME):c.1304A>G (p.Asn435Ser)	IGL, PRAME (N435S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3309663	NM_206956.3(PRAME):c.1293C>G (p.Ile431Met)	IGL, PRAME (I415M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318608	NM_206956.3(PRAME):c.1172C>T (p.Thr391Met)	IGL, PRAME (T375M +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2391635	NM_206956.3(PRAME):c.1078A>C (p.Met360Leu)	IGL, PRAME (M360L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205518	NM_206956.3(PRAME):c.1078A>G (p.Met360Val)	IGL, PRAME (M360V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218123	NM_206956.3(PRAME):c.1020G>A (p.Met340Ile)	IGL, PRAME (M340I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2401473	NM_206956.3(PRAME):c.1016T>C (p.Val339Ala)	IGL, PRAME (V323A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218122	NM_206956.3(PRAME):c.1009G>C (p.Gly337Arg)	IGL, PRAME (G321R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410473	NM_206956.3(PRAME):c.1004C>T (p.Ser335Leu)	IGL, PRAME (S335L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218133	NM_206956.3(PRAME):c.998G>A (p.Arg333Gln)	IGL, PRAME (R317Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526556	NM_206956.3(PRAME):c.967C>G (p.Pro323Ala)	IGL, PRAME (P307A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215112	NM_206956.3(PRAME):c.958G>T (p.Val320Leu)	IGL, PRAME (V304L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3218132	NM_206956.3(PRAME):c.833C>T (p.Pro278Leu)	IGL, PRAME (P262L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233100	NM_206956.3(PRAME):c.796C>T (p.Leu266Phe)	IGL, PRAME (L266F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295908	NM_206956.3(PRAME):c.794T>G (p.Leu265Arg)	IGL, PRAME (L265R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218130	NM_206956.3(PRAME):c.770G>A (p.Gly257Asp)	IGL, PRAME (G257D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361050	NM_206956.3(PRAME):c.749C>T (p.Ala250Val)	IGL, PRAME (A234V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218129	NM_206956.3(PRAME):c.697G>T (p.Asp233Tyr)	IGL, PRAME (D217Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408485	NM_206956.3(PRAME):c.692A>G (p.Gln231Arg)	IGL, PRAME (Q231R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225287	NM_206956.3(PRAME):c.671A>G (p.Lys224Arg)	IGL, PRAME (K224R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218128	NM_206956.3(PRAME):c.654G>T (p.Met218Ile)	IGL, PRAME (M202I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285894	NM_206956.3(PRAME):c.562T>C (p.Cys188Arg)	IGL, PRAME (C188R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382435	NM_206956.3(PRAME):c.514T>G (p.Phe172Val)	IGL, PRAME (F156V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238876	NM_206956.3(PRAME):c.403G>A (p.Val135Ile)	IGL, PRAME (V135I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457337	NM_206956.3(PRAME):c.374G>A (p.Arg125Gln)	IGL, PRAME (R109Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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