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Variants search result for Homo sapiens
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66 records found for search term Chi3l1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8560316CV23151single nucleotide variantNM_001276.2(CHI3L1):c.-131C>GAsthma-related traits, susceptibility to, 7 [RCV000008580]risk factor1203186754203186754Human2name
408394324CV3521878single nucleotide variantNM_001276.4(CHI3L1):c.258-2A>CSchizophrenia [RCV004764677]uncertain significance1203184634203184634Human2name
156325950CV2205504single nucleotide variantNM_001276.4(CHI3L1):c.14C>A (p.Ala5Glu)not specified [RCV004082439]uncertain significance1203186610203186610Humanname
156230890CV2348718single nucleotide variantNM_001276.4(CHI3L1):c.13G>A (p.Ala5Thr)not specified [RCV004201129]uncertain significance1203186611203186611Humanname
329366062CV2438059single nucleotide variantNM_001276.4(CHI3L1):c.14C>T (p.Ala5Val)not specified [RCV004256850]likely benign1203186610203186610Humanname
597770329CV3656570single nucleotide variantNM_001276.4(CHI3L1):c.23C>T (p.Thr8Ile)not specified [RCV004896686]uncertain significance1203186601203186601Humanname
401762174CV2722672single nucleotide variantNM_001276.4(CHI3L1):c.61G>A (p.Ala21Thr)not specified [RCV004325119]uncertain significance1203185380203185380Humanname
401865351CV2791622single nucleotide variantNM_001276.4(CHI3L1):c.540G>A (p.Ala180=)not specified [RCV004358984]likely benign1203182778203182778Humanname
405661553CV3300906single nucleotide variantNM_001276.4(CHI3L1):c.58T>G (p.Ser20Ala)not specified [RCV004439209]uncertain significance1203185383203185383Humanname
405661562CV3300909single nucleotide variantNM_001276.4(CHI3L1):c.86C>T (p.Thr29Ile)not specified [RCV004439212]uncertain significance1203185355203185355Humanname
597770293CV3656579single nucleotide variantNM_001276.4(CHI3L1):c.98A>G (p.Gln33Arg)not specified [RCV004896694]uncertain significance1203185343203185343Humanname
15191491CV718543single nucleotide variantNM_001276.4(CHI3L1):c.348C>A (p.Arg116=)not provided [RCV000888394]benign1203183758203183758Humanname
15191762CV732016single nucleotide variantNM_001276.4(CHI3L1):c.723G>A (p.Val241=)not provided [RCV000910342]benign1203180641203180641Humanname
156397437CV2200496single nucleotide variantNM_001276.4(CHI3L1):c.112G>A (p.Asp38Asn)not specified [RCV004078852]uncertain significance1203185329203185329Humanname
401736901CV2689518single nucleotide variantNM_001276.4(CHI3L1):c.199G>A (p.Asp67Asn)not specified [RCV004308356]uncertain significance1203185242203185242Humanname
401747377CV2698857single nucleotide variantNM_001276.4(CHI3L1):c.158A>T (p.His53Leu)not specified [RCV004301289]uncertain significance1203185283203185283Humanname
405661535CV3300900single nucleotide variantNM_001276.4(CHI3L1):c.133G>A (p.Ala45Thr)not specified [RCV004439203]uncertain significance1203185308203185308Humanname
597770320CV3656572single nucleotide variantNM_001276.4(CHI3L1):c.122G>C (p.Cys41Ser)not specified [RCV004896688]uncertain significance1203185319203185319Humanname
597770315CV3656573single nucleotide variantNM_001276.4(CHI3L1):c.232G>A (p.Gly78Ser)not specified [RCV004896689]uncertain significance1203185209203185209Humanname
597770311CV3656574single nucleotide variantNM_001276.4(CHI3L1):c.266A>G (p.Asn89Ser)not specified [RCV004896690]uncertain significance1203184624203184624Humanname
597770307CV3656575single nucleotide variantNM_001276.4(CHI3L1):c.216T>A (p.Asn72Lys)not specified [RCV004896691]uncertain significance1203185225203185225Humanname
598214308CV3951557single nucleotide variantNM_001276.4(CHI3L1):c.131A>C (p.Asp44Ala)not specified [RCV005316545]uncertain significance1203185310203185310Humanname
156323137CV2201517single nucleotide variantNM_001276.4(CHI3L1):c.371C>T (p.Pro124Leu)not specified [RCV004080008]uncertain significance1203183735203183735Humanname
156384816CV2231197single nucleotide variantNM_001276.4(CHI3L1):c.767T>C (p.Met256Thr)not specified [RCV004094397]uncertain significance1203180597203180597Humanname
156168805CV2299500single nucleotide variantNM_001276.4(CHI3L1):c.388C>A (p.His130Asn)not specified [RCV004154570]uncertain significance1203183718203183718Humanname
156262344CV2319780single nucleotide variantNM_001276.4(CHI3L1):c.476C>A (p.Ala159Asp)not specified [RCV004187310]uncertain significance1203182842203182842Humanname
156394846CV2328221single nucleotide variantNM_001276.4(CHI3L1):c.782T>C (p.Phe261Ser)not specified [RCV004173312]uncertain significance1203180582203180582Humanname
156333328CV2335972single nucleotide variantNM_001276.4(CHI3L1):c.689G>A (p.Ser230Asn)not specified [RCV004189581]uncertain significance1203181184203181184Humanname
155968202CV2337818single nucleotide variantNM_001276.4(CHI3L1):c.526G>A (p.Ala176Thr)not specified [RCV004183831]uncertain significance1203182792203182792Humanname
156255852CV2376732single nucleotide variantNM_001276.4(CHI3L1):c.779C>G (p.Thr260Ser)not specified [RCV004227016]uncertain significance1203180585203180585Humanname
156132712CV2382804single nucleotide variantNM_001276.4(CHI3L1):c.671G>A (p.Arg224Gln)not specified [RCV004224142]uncertain significance1203181202203181202Humanname
329354018CV2436782single nucleotide variantNM_001276.4(CHI3L1):c.910C>T (p.Arg304Cys)not specified [RCV004260186]uncertain significance1203179862203179862Humanname
329375247CV2440864single nucleotide variantNM_001276.4(CHI3L1):c.638G>A (p.Arg213His)not specified [RCV004261260]uncertain significance1203181235203181235Humanname
401758055CV2704148single nucleotide variantNM_001276.4(CHI3L1):c.950C>G (p.Pro317Arg)not specified [RCV004311164]uncertain significance1203179822203179822Humanname
401772110CV2708130single nucleotide variantNM_001276.4(CHI3L1):c.982T>C (p.Tyr328His)not specified [RCV004311504]uncertain significance1203179790203179790Humanname
401894851CV2781907single nucleotide variantNM_001276.4(CHI3L1):c.626A>G (p.His209Arg)not specified [RCV004357150]uncertain significance1203181247203181247Humanname
405661537CV3300901single nucleotide variantNM_001276.4(CHI3L1):c.304G>T (p.Gly102Trp)not specified [RCV004439204]uncertain significance1203184586203184586Humanname
405661541CV3300902single nucleotide variantNM_001276.4(CHI3L1):c.349C>T (p.Arg117Trp)not specified [RCV004439205]uncertain significance1203183757203183757Humanname
405661544CV3300903single nucleotide variantNM_001276.4(CHI3L1):c.382C>T (p.Arg128Cys)not specified [RCV004439206]uncertain significance1203183724203183724Humanname
405661547CV3300904single nucleotide variantNM_001276.4(CHI3L1):c.539C>T (p.Ala180Val)not specified [RCV004439207]uncertain significance1203182779203182779Humanname
405661550CV3300905single nucleotide variantNM_001276.4(CHI3L1):c.578A>G (p.Lys193Arg)not specified [RCV004439208]uncertain significance1203182740203182740Humanname
405661556CV3300907single nucleotide variantNM_001276.4(CHI3L1):c.689G>T (p.Ser230Ile)not specified [RCV004439210]uncertain significance1203181184203181184Humanname
405661559CV3300908single nucleotide variantNM_001276.4(CHI3L1):c.730A>C (p.Met244Leu)not specified [RCV004439211]uncertain significance1203180634203180634Humanname
407455461CV3422697single nucleotide variantNM_001276.4(CHI3L1):c.937G>A (p.Gly313Ser)not specified [RCV004610325]uncertain significance1203179835203179835Humanname
407455466CV3422699single nucleotide variantNM_001276.4(CHI3L1):c.616T>C (p.Tyr206His)not specified [RCV004610327]uncertain significance1203181257203181257Humanname
407455468CV3422700single nucleotide variantNM_001276.4(CHI3L1):c.998G>T (p.Ser333Ile)not specified [RCV004610328]uncertain significance1203179774203179774Humanname
407455471CV3422701single nucleotide variantNM_001276.4(CHI3L1):c.820G>A (p.Val274Ile)not specified [RCV004610329]uncertain significance1203180544203180544Humanname
597770325CV3656571single nucleotide variantNM_001276.4(CHI3L1):c.446A>C (p.His149Pro)not specified [RCV004896687]uncertain significance1203183660203183660Humanname
597770302CV3656576single nucleotide variantNM_001276.4(CHI3L1):c.877A>G (p.Thr293Ala)not specified [RCV004896692]uncertain significance1203180487203180487Humanname
597770288CV3656580single nucleotide variantNM_001276.4(CHI3L1):c.298A>G (p.Asn100Asp)not specified [RCV004896695]uncertain significance1203184592203184592Humanname
598214283CV3951551single nucleotide variantNM_001276.4(CHI3L1):c.592C>G (p.Leu198Val)not specified [RCV005316540]uncertain significance1203181281203181281Humanname
598214298CV3951554single nucleotide variantNM_001276.4(CHI3L1):c.409C>G (p.Leu137Val)not specified [RCV005316543]uncertain significance1203183697203183697Humanname
598264381CV3951555single nucleotide variantNM_001276.4(CHI3L1):c.784G>A (p.Gly262Arg)not specified [RCV005326118]uncertain significance1203180580203180580Humanname
598214315CV3951558single nucleotide variantNM_001276.4(CHI3L1):c.617A>G (p.Tyr206Cys)not specified [RCV005316546]uncertain significance1203181256203181256Humanname
598214327CV3951560single nucleotide variantNM_001276.4(CHI3L1):c.983A>G (p.Tyr328Cys)not specified [RCV005316548]uncertain significance1203179789203179789Humanname
616938796CV4015878single nucleotide variantNM_001276.4(CHI3L1):c.433A>G (p.Arg145Gly)Thalidomide response [RCV005414430]drug response1203183673203183673Humanname
401752136CV2682714single nucleotide variantNM_001276.4(CHI3L1):c.1082G>A (p.Gly361Asp)not specified [RCV004281694]uncertain significance1203179515203179515Humanname
401744313CV2696979single nucleotide variantNM_001276.4(CHI3L1):c.1088T>G (p.Phe363Cys)not specified [RCV004292971]uncertain significance1203179509203179509Humanname
401891190CV2769131single nucleotide variantNM_001276.4(CHI3L1):c.1004A>G (p.Lys335Arg)not specified [RCV004348979]uncertain significance1203179768203179768Humanname
405661532CV3300899single nucleotide variantNM_001276.4(CHI3L1):c.1040C>T (p.Ala347Val)not specified [RCV004439202]uncertain significance1203179557203179557Humanname
407455463CV3422698single nucleotide variantNM_001276.4(CHI3L1):c.1148C>T (p.Thr383Met)not specified [RCV004610326]uncertain significance1203179449203179449Humanname
597770333CV3656569single nucleotide variantNM_001276.4(CHI3L1):c.1144G>T (p.Ala382Ser)not specified [RCV004896685]uncertain significance1203179453203179453Humanname
598214288CV3951552single nucleotide variantNM_001276.4(CHI3L1):c.1045G>A (p.Ala349Thr)not specified [RCV005316541]uncertain significance1203179552203179552Humanname
598214303CV3951556single nucleotide variantNM_001276.4(CHI3L1):c.1135G>A (p.Ala379Thr)not specified [RCV005316544]uncertain significance1203179462203179462Humanname
598214321CV3951559single nucleotide variantNM_001276.4(CHI3L1):c.1048A>G (p.Met350Val)not specified [RCV005316547]uncertain significance1203179549203179549Humanname
598124931CV3885480duplicationNM_001276.4(CHI3L1):c.722_725dup (p.Tyr243fs)not specified [RCV005240058]uncertain significance1203180638203180639Humanname