ClinVar for Gene (Select 121227) - ClinVar

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Links from Gene

Items: 81

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3291337	NM_153377.5(LRIG3):c.2599A>G (p.Arg867Gly)	LRIG3 (R807G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291336	NM_153377.5(LRIG3):c.2062A>G (p.Asn688Asp)	LRIG3 (N628D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291335	NM_153377.5(LRIG3):c.1690A>G (p.Thr564Ala)	LRIG3 (T504A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291334	NM_153377.5(LRIG3):c.335C>T (p.Thr112Ile)	LRIG3 (T52I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291333	NM_153377.5(LRIG3):c.1638G>A (p.Met546Ile)	LRIG3 (M546I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291332	NM_153377.5(LRIG3):c.1505C>T (p.Thr502Met)	LRIG3 (T442M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291331	NM_153377.5(LRIG3):c.2665G>A (p.Gly889Arg)	LRIG3 (G829R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291330	NM_153377.5(LRIG3):c.224G>C (p.Trp75Ser)	LRIG3 (W75S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291328	NM_153377.5(LRIG3):c.2336A>G (p.Asn779Ser)	LRIG3 (N779S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291327	NM_153377.5(LRIG3):c.842G>C (p.Gly281Ala)	LOC126861547, LRIG3 (G281A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291326	NM_153377.5(LRIG3):c.320A>G (p.Asn107Ser)	LRIG3 (N47S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291325	NM_153377.5(LRIG3):c.1675G>T (p.Val559Leu)	LRIG3 (V499L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120066	NM_153377.5(LRIG3):c.941G>A (p.Ser314Asn)	LOC126861547, LRIG3 (S254N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120065	NM_153377.5(LRIG3):c.92G>A (p.Gly31Asp)	LRIG3 (G31D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120064	NM_153377.5(LRIG3):c.913G>A (p.Asp305Asn)	LOC126861547, LRIG3 (D245N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120063	NM_153377.5(LRIG3):c.499C>G (p.Leu167Val)	LRIG3 (L107V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120062	NM_153377.5(LRIG3):c.3076C>T (p.Pro1026Ser)	LRIG3 (P966S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120061	NM_153377.5(LRIG3):c.2952C>A (p.Ser984Arg)	LRIG3 (S924R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120060	NM_153377.5(LRIG3):c.2941T>A (p.Cys981Ser)	LRIG3 (C981S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120059	NM_153377.5(LRIG3):c.2777C>T (p.Thr926Ile)	LRIG3 (T866I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120058	NM_153377.5(LRIG3):c.2245A>C (p.Asn749His)	LRIG3 (N749H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120057	NM_153377.5(LRIG3):c.2200G>A (p.Asp734Asn)	LRIG3 (D674N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120056	NM_153377.5(LRIG3):c.1984T>C (p.Phe662Leu)	LRIG3 (F602L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120055	NM_153377.5(LRIG3):c.1869G>C (p.Glu623Asp)	LRIG3 (E623D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120054	NM_153377.5(LRIG3):c.1478G>T (p.Cys493Phe)	LRIG3 (C493F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120053	NM_153377.5(LRIG3):c.1169G>A (p.Arg390Gln)	LRIG3 (R390Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3063261	GRCh37/hg19 12q14.1(chr12:59148987-59769685)x1	LRIG3	Copy number loss	not specified	GUncertain significance
Select item 2643155	NM_153377.5(LRIG3):c.1380G>A (p.Ala460=)	LRIG3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2643154	NM_153377.5(LRIG3):c.2019A>G (p.Val673=)	LRIG3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2599356	NM_153377.5(LRIG3):c.661G>A (p.Glu221Lys)	LRIG3 (E221K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2560086	NM_153377.5(LRIG3):c.1849G>A (p.Gly617Arg)	LRIG3 (G557R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554082	NM_153377.5(LRIG3):c.1283A>G (p.Asn428Ser)	LRIG3 (N368S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543161	NM_153377.5(LRIG3):c.3158A>G (p.Tyr1053Cys)	LRIG3 (Y993C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542035	NM_153377.5(LRIG3):c.2338G>A (p.Val780Met)	LRIG3 (V720M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514360	NM_153377.5(LRIG3):c.3098C>G (p.Ser1033Trp)	LRIG3 (S1033W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510732	NM_153377.5(LRIG3):c.1583C>G (p.Ser528Cys)	LRIG3 (S468C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2498574	GRCh37/hg19 12q13.3-14.1(chr12:57064059-59314016)x1	AGAP2, ARHGAP9 +45 more	Copy number loss	not provided	GLikely pathogenic
Select item 2494399	NM_153377.5(LRIG3):c.1969G>A (p.Glu657Lys)	LRIG3 (E657K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493780	NM_153377.5(LRIG3):c.1733A>G (p.Lys578Arg)	LRIG3 (K518R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488961	NM_153377.5(LRIG3):c.2112G>C (p.Leu704Phe)	LRIG3 (L704F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411359	NM_153377.5(LRIG3):c.2759G>A (p.Cys920Tyr)	LRIG3 (C860Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408895	NM_153377.5(LRIG3):c.1055A>T (p.Asp352Val)	LOC126861547, LRIG3 (D352V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399018	NM_153377.5(LRIG3):c.2491T>C (p.Tyr831His)	LRIG3 (Y771H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397349	NM_153377.5(LRIG3):c.1990G>A (p.Val664Met)	LRIG3 (V664M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389713	NM_153377.5(LRIG3):c.524A>G (p.Asn175Ser)	LRIG3 (N175S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383305	NM_153377.5(LRIG3):c.3287A>G (p.His1096Arg)	LRIG3 (H1036R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378570	NM_153377.5(LRIG3):c.2503C>T (p.Arg835Trp)	LRIG3 (R775W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377801	NM_153377.5(LRIG3):c.1526C>T (p.Ser509Leu)	LRIG3 (S509L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366527	NM_153377.5(LRIG3):c.2342G>A (p.Arg781His)	LRIG3 (R721H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363496	NM_153377.5(LRIG3):c.7G>T (p.Ala3Ser)	LRIG3 (A3S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362494	NM_153377.5(LRIG3):c.1657C>T (p.Arg553Trp)	LRIG3 (R493W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353471	NM_153377.5(LRIG3):c.118G>A (p.Gly40Arg)	LOC130008170, LRIG3 (G40R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329680	NM_153377.5(LRIG3):c.943G>A (p.Glu315Lys)	LOC126861547, LRIG3 (E315K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324658	NM_153377.5(LRIG3):c.533G>A (p.Arg178Gln)	LRIG3 (R118Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309547	NM_153377.5(LRIG3):c.1190G>A (p.Arg397Gln)	LRIG3 (R337Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306299	NM_153377.5(LRIG3):c.2279G>T (p.Ser760Ile)	LRIG3 (S760I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302450	NM_153377.5(LRIG3):c.2233T>C (p.Phe745Leu)	LRIG3 (F685L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301938	NM_153377.5(LRIG3):c.1847C>A (p.Ala616Asp)	LRIG3 (A616D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286680	NM_153377.5(LRIG3):c.1664A>G (p.Gln555Arg)	LRIG3 (Q495R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283045	NM_153377.5(LRIG3):c.424A>G (p.Lys142Glu)	LRIG3 (K142E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273096	NM_153377.5(LRIG3):c.2101C>T (p.Arg701Trp)	LRIG3 (R641W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271436	NM_153377.5(LRIG3):c.2551C>T (p.Pro851Ser)	LRIG3 (P851S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248071	NM_153377.5(LRIG3):c.2102G>T (p.Arg701Leu)	LRIG3 (R641L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246016	NM_153377.5(LRIG3):c.914A>T (p.Asp305Val)	LOC126861547, LRIG3 (D245V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235691	NM_153377.5(LRIG3):c.1063T>C (p.Phe355Leu)	LOC126861547, LRIG3 (F295L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 980440	GRCh37/hg19 12q14.1(chr12:59136522-62410625)x1	SLC16A7, LRIG3 +1 more	Copy number loss	not provided	GUncertain significance
Select item 815528	GRCh37/hg19 12q13.2-14.1(chr12:55552371-62126304)x3	AGAP2, ANKRD52 +105 more	Copy number gain	not provided	GPathogenic
Select item 781085	NM_153377.5(LRIG3):c.2634CCA[2] (p.His880del)	LRIG3 (H820del +1 more)	Microsatellite (inframe_deletion)	not provided	GBenign
Select item 776901	NM_153377.5(LRIG3):c.2694T>A (p.Ser898Arg)	LRIG3 (S838R +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 715584	NM_153377.5(LRIG3):c.1132A>G (p.Met378Val)	LRIG3 (M318V +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 563960	GRCh37/hg19 12q14.1(chr12:58544526-59353323)x3	LRIG3	Copy number gain	not provided	GUncertain significance
Select item 563954	GRCh37/hg19 12q14.1(chr12:59148987-59769685)x1	LRIG3	Copy number loss	not provided	GUncertain significance
Select item 441984	GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)	SLC15A5, SLC16A7 +1006 more	Copy number gain	See cases	GPathogenic
Select item 441983	GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)x3	A2M, A2ML1 +1006 more	Copy number gain	See cases	GPathogenic
Select item 395032	GRCh37/hg19 12q14.1(chr12:59167152-60244566)x3	LRIG3, SLC16A7	Copy number gain	See cases	GLikely benign
Select item 268075	GRCh37/hg19 12p13.33-q24.33(chr12:1-133851895)x3	GALNT8, H2AJ +1007 more	Copy number gain	See cases	GPathogenic
Select item 155208	GRCh38/hg38 12q14.1(chr12:58802649-59703763)x3	LINC02448, LOC100506869 +24 more	Copy number gain	See cases	GUncertain significance
Select item 150740	GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3	ACAD10, ACADS +4836 more	Copy number gain	See cases	GPathogenic
Select item 59020	GRCh38/hg38 12q13.3-14.1(chr12:57041158-60273934)x1	AGAP2, AGAP2-AS1 +162 more	Copy number loss	See cases	GPathogenic
Select item 59019	GRCh38/hg38 12q13.3-14.2(chr12:57013355-63042498)x1	AGAP2, AGAP2-AS1 +199 more	Copy number loss	See cases	GPathogenic
Select item 34221	GRCh38/hg38 12q14.1(chr12:58773370-59370427)x1	LINC02388, LOC100506869 +17 more	Copy number loss	See cases	GUncertain significance

ClinVar

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Germline classification

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Links from Gene

Items: 81