IQGAP2[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58096	GRCh38/hg38 5q13.3-22.1(chr5:74163186-110809453)x3	ENC1, ERAP1 +690 more	Copy number gain	See cases	GPathogenic
Select item 2598577	NM_006633.5(IQGAP2):c.20C>A (p.Pro7Gln)	IQGAP2 (P7Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 729524	NM_006633.5(IQGAP2):c.34C>A (p.Pro12Thr)	IQGAP2 (P12T)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 723267	NM_006633.5(IQGAP2):c.57C>T (p.Asp19=)	IQGAP2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2611223	NM_006633.5(IQGAP2):c.89A>G (p.Glu30Gly)	IQGAP2 (E30G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206410	NM_006633.5(IQGAP2):c.115G>A (p.Glu39Lys)	IQGAP2 (E39K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 152763	GRCh38/hg38 5q13.3(chr5:76534282-76608747)x1	IQGAP2, LOC101929109 +4 more	Copy number loss	See cases	GUncertain significance
Select item 2614032	NM_006633.5(IQGAP2):c.173A>T (p.Glu58Val)	IQGAP2 (E58V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612238	NM_006633.5(IQGAP2):c.188C>T (p.Thr63Ile)	IQGAP2 (T63I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474666	NM_006633.5(IQGAP2):c.209G>A (p.Arg70Gln)	IQGAP2 (R20Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110608	NM_006633.5(IQGAP2):c.221A>T (p.Tyr74Phe)	IQGAP2 (Y74F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301498	NM_006633.5(IQGAP2):c.269A>T (p.Lys90Ile)	IQGAP2 (K90I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460751	NM_006633.5(IQGAP2):c.295C>T (p.Arg99Cys)	IQGAP2 (R99C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 252669	NM_006633.5(IQGAP2):c.322C>T (p.Arg108Ter)	IQGAP2 (R108* +1 more)	Single nucleotide variant (nonsense)	not specified	GUncertain significance
Select item 2257683	NM_006633.5(IQGAP2):c.329C>T (p.Thr110Ile)	IQGAP2 (T60I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257559	NM_006633.5(IQGAP2):c.340G>A (p.Val114Ile)	IQGAP2 (V114I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110618	NM_006633.5(IQGAP2):c.358A>C (p.Met120Leu)	IQGAP2 (M70L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244877	NM_006633.5(IQGAP2):c.391C>G (p.Pro131Ala)	IQGAP2 (P131A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257526	NM_006633.5(IQGAP2):c.419A>G (p.Lys140Arg)	IQGAP2 (K90R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1232742	NM_006633.5(IQGAP2):c.462G>A (p.Leu154=)	IQGAP2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3110623	NM_006633.5(IQGAP2):c.467T>A (p.Leu156Gln)	IQGAP2 (L156Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110624	NM_006633.5(IQGAP2):c.487C>A (p.Pro163Thr)	IQGAP2 (P163T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248275	NM_006633.5(IQGAP2):c.493A>G (p.Ile165Val)	IQGAP2 (I165V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 720792	NM_006633.5(IQGAP2):c.700G>A (p.Val234Ile)	IQGAP2 (V184I +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2235452	NM_006633.5(IQGAP2):c.706A>T (p.Thr236Ser)	IQGAP2 (T186S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480818	NM_006633.5(IQGAP2):c.710T>C (p.Leu237Pro)	IQGAP2 (L187P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211478	NM_006633.5(IQGAP2):c.905A>C (p.Asn302Thr)	IQGAP2 (N252T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542426	NM_006633.5(IQGAP2):c.932A>G (p.Asn311Ser)	IQGAP2 (N261S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403771	NM_006633.5(IQGAP2):c.937G>C (p.Val313Leu)	IQGAP2 (V263L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110626	NM_006633.5(IQGAP2):c.992C>T (p.Ala331Val)	IQGAP2 (A281V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110601	NM_006633.5(IQGAP2):c.1022C>T (p.Ala341Val)	IQGAP2 (A291V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612701	NM_006633.5(IQGAP2):c.1127C>A (p.Ala376Asp)	IQGAP2 (A326D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110602	NM_006633.5(IQGAP2):c.1192G>A (p.Ala398Thr)	IQGAP2 (A348T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3110603	NM_006633.5(IQGAP2):c.1208A>G (p.Asn403Ser)	IQGAP2 (N403S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544003	NM_006633.5(IQGAP2):c.1216A>C (p.Lys406Gln)	IQGAP2 (K356Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522490	NM_006633.5(IQGAP2):c.1231C>T (p.Arg411Cys)	IQGAP2 (R411C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265298	NM_006633.5(IQGAP2):c.1321G>A (p.Asp441Asn)	IQGAP2 (D441N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303330	NM_006633.5(IQGAP2):c.1325T>C (p.Met442Thr)	IQGAP2 (M392T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 786059	NM_006633.5(IQGAP2):c.1436C>A (p.Pro479His)	IQGAP2 (P429H +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3110605	NM_006633.5(IQGAP2):c.1460A>G (p.Asp487Gly)	IQGAP2 (D437G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 780542	NM_006633.5(IQGAP2):c.1470T>C (p.His490=)	IQGAP2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2272119	NM_004101.4(F2RL2):c.1060G>A (p.Asp354Asn)	F2RL2, IQGAP2 (D354N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2551400	NM_004101.4(F2RL2):c.944C>T (p.Ala315Val)	F2RL2, IQGAP2 (A293V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2489971	NM_004101.4(F2RL2):c.904G>A (p.Ala302Thr)	F2RL2, IQGAP2 (A280T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3091440	NM_004101.4(F2RL2):c.880C>T (p.His294Tyr)	F2RL2, IQGAP2 (H272Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2513200	NM_004101.4(F2RL2):c.877G>T (p.Asp293Tyr)	F2RL2, IQGAP2 (D271Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2489316	NM_004101.4(F2RL2):c.839A>G (p.Tyr280Cys)	F2RL2, IQGAP2 (Y258C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2239978	NM_004101.4(F2RL2):c.784T>G (p.Tyr262Asp)	F2RL2, IQGAP2 (Y240D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2554479	NM_004101.4(F2RL2):c.670T>C (p.Tyr224His)	F2RL2, IQGAP2 (Y202H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3091438	NM_004101.4(F2RL2):c.578T>C (p.Leu193Pro)	F2RL2, IQGAP2 (L193P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2247011	NM_004101.4(F2RL2):c.554C>T (p.Ala185Val)	F2RL2, IQGAP2 (A163V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3091437	NM_004101.4(F2RL2):c.503C>A (p.Ala168Asp)	F2RL2, IQGAP2 (A168D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2489268	NM_004101.4(F2RL2):c.503C>G (p.Ala168Gly)	F2RL2, IQGAP2 (A146G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2466105	NM_004101.4(F2RL2):c.403C>G (p.Leu135Val)	F2RL2, IQGAP2 (L135V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2339093	NM_004101.4(F2RL2):c.379T>C (p.Cys127Arg)	F2RL2, IQGAP2 (C105R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2341780	NM_004101.4(F2RL2):c.230A>G (p.His77Arg)	F2RL2, IQGAP2 (H55R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3091436	NM_004101.4(F2RL2):c.222T>G (p.Ser74Arg)	F2RL2, IQGAP2 (S52R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2313227	NM_004101.4(F2RL2):c.205A>G (p.Lys69Glu)	F2RL2, IQGAP2 (K47E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2383493	NM_004101.4(F2RL2):c.188C>T (p.Thr63Met)	F2RL2, IQGAP2 (T41M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2370541	NM_004101.4(F2RL2):c.173G>A (p.Gly58Asp)	F2RL2, IQGAP2 (G36D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 587553	NM_004101.4(F2RL2):c.160del (p.Ser54fs)	F2RL2, IQGAP2 (S32fs +1 more)	Deletion (frameshift variant +1 more)	not provided	GUncertain significance
Select item 2387618	NM_004101.4(F2RL2):c.134C>T (p.Pro45Leu)	F2RL2, IQGAP2 (P45L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2609858	NM_004101.4(F2RL2):c.127G>A (p.Ala43Thr)	F2RL2, IQGAP2 (A21T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2594178	NM_004101.4(F2RL2):c.121C>T (p.Arg41Cys)	F2RL2, IQGAP2 (R19C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2363808	NM_006633.5(IQGAP2):c.1576G>A (p.Asp526Asn)	IQGAP2 (D79N +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2397652	NM_006633.5(IQGAP2):c.1739A>G (p.Tyr580Cys)	IQGAP2 (Y580C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110606	NM_006633.5(IQGAP2):c.1792G>A (p.Gly598Ser)	IQGAP2 (G151S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110607	NM_006633.5(IQGAP2):c.1808T>G (p.Leu603Arg)	IQGAP2 (L156R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337928	NM_006633.5(IQGAP2):c.1832A>G (p.Tyr611Cys)	IQGAP2 (Y164C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534056	NM_006633.5(IQGAP2):c.1921G>A (p.Glu641Lys)	IQGAP2 (E591K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 787286	NM_006633.5(IQGAP2):c.1939G>C (p.Val647Leu)	IQGAP2 (V597L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2323433	NM_006633.5(IQGAP2):c.1957C>T (p.Arg653Cys)	IQGAP2 (R603C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2474407	NM_006633.5(IQGAP2):c.1971G>T (p.Trp657Cys)	IQGAP2 (W657C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2540199	NM_006633.5(IQGAP2):c.1996C>T (p.Arg666Cys)	IQGAP2 (R616C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2233789	NM_006633.5(IQGAP2):c.2020C>A (p.Pro674Thr)	IQGAP2 (P674T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2301689	NM_006633.5(IQGAP2):c.2030G>A (p.Arg677Lys)	IQGAP2 (R677K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2276791	NM_006633.5(IQGAP2):c.2077A>T (p.Asn693Tyr)	IQGAP2 (N643Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2520373	NM_006633.5(IQGAP2):c.2190G>C (p.Trp730Cys)	IQGAP2 (W680C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512490	NM_006633.5(IQGAP2):c.2221C>T (p.Leu741Phe)	IQGAP2 (L691F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110609	NM_006633.5(IQGAP2):c.2235G>T (p.Gln745His)	IQGAP2 (Q745H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 754434	NM_006633.5(IQGAP2):c.2289G>A (p.Ala763=)	IQGAP2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2324470	NM_006633.5(IQGAP2):c.2302G>A (p.Asp768Asn)	IQGAP2 (D264N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276368	NM_006633.5(IQGAP2):c.2304T>G (p.Asp768Glu)	IQGAP2 (D718E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110610	NM_006633.5(IQGAP2):c.2353C>T (p.Arg785Cys)	IQGAP2 (R735C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345119	NM_006633.5(IQGAP2):c.2354G>A (p.Arg785His)	IQGAP2 (R281H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509765	NM_006633.5(IQGAP2):c.2671C>T (p.Leu891Phe)	IQGAP2 (L841F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110611	NM_006633.5(IQGAP2):c.2765T>C (p.Leu922Pro)	IQGAP2 (L418P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216594	NM_006633.5(IQGAP2):c.2768A>G (p.Tyr923Cys)	IQGAP2 (Y873C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110612	NM_006633.5(IQGAP2):c.2797T>A (p.Tyr933Asn)	IQGAP2 (Y429N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110613	NM_006633.5(IQGAP2):c.2919A>C (p.Arg973Ser)	IQGAP2 (R469S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378625	NM_006633.5(IQGAP2):c.2980G>A (p.Asp994Asn)	IQGAP2 (D944N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 770912	NM_006633.5(IQGAP2):c.2982C>T (p.Asp994=)	IQGAP2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2371022	NM_006633.5(IQGAP2):c.3002A>G (p.Asn1001Ser)	IQGAP2 (N1001S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544956	NM_006633.5(IQGAP2):c.3136G>T (p.Ala1046Ser)	IQGAP2 (A1046S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 791444	NM_006633.5(IQGAP2):c.3155G>T (p.Arg1052Ile)	IQGAP2 (R1002I +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2325271	NM_006633.5(IQGAP2):c.3184A>G (p.Ile1062Val)	IQGAP2 (I1012V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 717196	NM_006633.5(IQGAP2):c.3234A>G (p.Lys1078=)	IQGAP2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2276166	NM_006633.5(IQGAP2):c.3254A>T (p.His1085Leu)	IQGAP2 (H1085L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110615	NM_006633.5(IQGAP2):c.3311T>A (p.Leu1104Gln)	IQGAP2 (L1054Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110616	NM_006633.5(IQGAP2):c.3325A>C (p.Met1109Leu)	IQGAP2 (M1059L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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