"Ambry Genetics"[submitter] AND "IL4R"[gene] - ClinVar

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Items: 51

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3285892	NM_000418.4(IL4R):c.28T>A (p.Phe10Ile)	IL4R (F10I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109439	NM_000418.4(IL4R):c.133G>A (p.Glu45Lys)	IL4R (E45K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2457376	NM_000418.4(IL4R):c.169G>A (p.Glu57Lys)	IL4R (E42K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2361862	NM_000418.4(IL4R):c.175C>T (p.Arg59Cys)	IL4R (R59C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109448	NM_000418.4(IL4R):c.245C>T (p.Ala82Val)	IL4R (A82V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3285898	NM_000418.4(IL4R):c.277G>A (p.Val93Met)	IL4R (V78M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2360543	NM_000418.4(IL4R):c.355G>A (p.Glu119Lys)	IL4R (E104K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2544207	NM_000418.4(IL4R):c.370A>G (p.Arg124Gly)	IL4R (R109G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109449	NM_000418.4(IL4R):c.437C>T (p.Pro146Leu)	IL4R (P131L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3285897	NM_000418.4(IL4R):c.472A>T (p.Thr158Ser)	IL4R (T143S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2249995	NM_000418.4(IL4R):c.496G>C (p.Glu166Gln)	IL4R (E151Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109450	NM_000418.4(IL4R):c.520A>G (p.Ile174Val)	IL4R (I174V +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2253102	NM_000418.4(IL4R):c.595G>A (p.Ala199Thr)	IL4R (A39T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224161	NM_000418.4(IL4R):c.601G>A (p.Val201Met)	IL4R (V186M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265949	NM_000418.4(IL4R):c.648C>A (p.Ser216Arg)	IL4R (S201R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488041	NM_000418.4(IL4R):c.687C>G (p.Phe229Leu)	IL4R (F69L +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3109451	NM_000418.4(IL4R):c.688G>A (p.Glu230Lys)	IL4R (E230K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480869	NM_000418.4(IL4R):c.817C>T (p.Arg273Cys)	IL4R (R273C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277811	NM_000418.4(IL4R):c.818G>A (p.Arg273His)	IL4R (R258H +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2317710	NM_000418.4(IL4R):c.832A>G (p.Ile278Val)	IL4R (I118V +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3109452	NM_000418.4(IL4R):c.875G>A (p.Arg292Gln)	IL4R (R132Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554912	NM_000418.4(IL4R):c.929T>C (p.Leu310Ser)	IL4R (L150S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348751	NM_000418.4(IL4R):c.968A>T (p.Asp323Val)	IL4R (D163V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109435	NM_000418.4(IL4R):c.1072G>A (p.Val358Met)	IL4R (V343M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493213	NM_000418.4(IL4R):c.1119G>C (p.Glu373Asp)	IL4R (E213D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109437	NM_000418.4(IL4R):c.1178A>T (p.Asp393Val)	IL4R (D378V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285894	NM_000418.4(IL4R):c.1247G>A (p.Gly416Glu)	IL4R (G416E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109438	NM_000418.4(IL4R):c.1281G>T (p.Met427Ile)	IL4R (M412I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109440	NM_000418.4(IL4R):c.1379G>A (p.Gly460Asp)	IL4R (G460D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302165	NM_000418.4(IL4R):c.1379G>T (p.Gly460Val)	IL4R (G300V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317709	NM_000418.4(IL4R):c.1439A>G (p.Asp480Gly)	IL4R (D480G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355062	NM_000418.4(IL4R):c.1565A>G (p.His522Arg)	IL4R (H362R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491382	NM_000418.4(IL4R):c.1663C>T (p.Arg555Cys)	IL4R (R555C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285895	NM_000418.4(IL4R):c.1664G>A (p.Arg555His)	IL4R (R555H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340670	NM_000418.4(IL4R):c.1675C>G (p.Leu559Val)	IL4R (L399V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109441	NM_000418.4(IL4R):c.1760C>T (p.Thr587Ile)	IL4R (T427I +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3109442	NM_000418.4(IL4R):c.1840G>A (p.Ala614Thr)	IL4R (A454T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540571	NM_000418.4(IL4R):c.1913T>C (p.Ile638Thr)	IL4R (I623T +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3109443	NM_000418.4(IL4R):c.1994C>T (p.Pro665Leu)	IL4R (P505L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271905	NM_000418.4(IL4R):c.2026G>C (p.Glu676Gln)	IL4R (E516Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329110	NM_000418.4(IL4R):c.2048G>A (p.Gly683Glu)	IL4R (G523E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320468	NM_000418.4(IL4R):c.2057T>C (p.Val686Ala)	IL4R (V526A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285893	NM_000418.4(IL4R):c.2068C>T (p.Pro690Ser)	IL4R (P675S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594841	NM_000418.4(IL4R):c.2077C>T (p.Pro693Ser)	IL4R (P533S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109445	NM_000418.4(IL4R):c.2107C>G (p.Leu703Val)	IL4R (L543V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109446	NM_000418.4(IL4R):c.2128G>A (p.Gly710Ser)	IL4R (G710S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109447	NM_000418.4(IL4R):c.2248G>A (p.Asp750Asn)	IL4R (D750N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2269351	NM_000418.4(IL4R):c.2249A>G (p.Asp750Gly)	IL4R (D735G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289123	NM_000418.4(IL4R):c.2413T>G (p.Ser805Ala)	IL4R (S805A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491875	NM_000418.4(IL4R):c.2425C>T (p.Pro809Ser)	IL4R (P649S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590128	NM_000418.4(IL4R):c.2443G>A (p.Val815Ile)	IL4R (V655I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 51