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Variants search result for Homo sapiens
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45 records found for search term Lamp3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8578454CV112836single nucleotide variantNM_014398.3(LAMP3):c.889-3924C>GLung cancer [RCV000093359]uncertain significance3183144519183144519Humanname
155932962CV2372196single nucleotide variantNM_014398.4(LAMP3):c.61G>A (p.Asp21Asn)not specified [RCV004216976]uncertain significance3183154380183154380Humanname
405814882CV3273071single nucleotide variantNM_014398.4(LAMP3):c.29C>T (p.Ala10Val)not specified [RCV004410060]likely benign3183162627183162627Humanname
405814889CV3273074single nucleotide variantNM_014398.4(LAMP3):c.61G>T (p.Asp21Tyr)not specified [RCV004410063]likely benign3183154380183154380Humanname
156080225CV2292676single nucleotide variantNM_014398.4(LAMP3):c.224T>C (p.Phe75Ser)not specified [RCV004154362]likely benign3183154217183154217Humanname
156161054CV2398238single nucleotide variantNM_014398.4(LAMP3):c.217A>C (p.Ile73Leu)not specified [RCV004235151]uncertain significance3183154224183154224Humanname
401875615CV2766113single nucleotide variantNM_014398.4(LAMP3):c.278A>G (p.Asn93Ser)not specified [RCV004340568]likely benign3183154163183154163Humanname
405814878CV3273069single nucleotide variantNM_014398.4(LAMP3):c.155T>C (p.Val52Ala)not specified [RCV004410058]uncertain significance3183154286183154286Humanname
405814880CV3273070single nucleotide variantNM_014398.4(LAMP3):c.265G>A (p.Ala89Thr)not specified [RCV004410059]uncertain significance3183154176183154176Humanname
598197489CV3987581single nucleotide variantNM_014398.4(LAMP3):c.206T>C (p.Met69Thr)not specified [RCV005355367]likely benign3183154235183154235Humanname
8630700CV85855single nucleotide variantNM_014398.3(LAMP3):c.1047C>T (p.Ala349=)Malignant melanoma [RCV000065939]not provided3183135787183135787Humanname
156319216CV2260801single nucleotide variantNM_014398.4(LAMP3):c.976G>A (p.Val326Met)not specified [RCV004125716]likely benign3183135858183135858Humanname
156054813CV2269606single nucleotide variantNM_014398.4(LAMP3):c.487A>G (p.Ser163Gly)not specified [RCV004124701]uncertain significance3183153954183153954Humanname
155944201CV2295058single nucleotide variantNM_014398.4(LAMP3):c.646C>G (p.Leu216Val)not specified [RCV004156176]uncertain significance3183153795183153795Humanname
156166879CV2315265single nucleotide variantNM_014398.4(LAMP3):c.809C>A (p.Ala270Asp)not specified [RCV004167254]uncertain significance3183152454183152454Humanname
156278739CV2325118single nucleotide variantNM_014398.4(LAMP3):c.814G>A (p.Gly272Arg)not specified [RCV004175647]uncertain significance3183152449183152449Humanname
156188222CV2395384single nucleotide variantNM_014398.4(LAMP3):c.830G>A (p.Arg277Gln)not specified [RCV004239473]likely benign3183152433183152433Humanname
156095070CV2398907single nucleotide variantNM_014398.4(LAMP3):c.803C>T (p.Thr268Met)not specified [RCV004245222]uncertain significance3183152460183152460Humanname
329381040CV2440608single nucleotide variantNM_014398.4(LAMP3):c.391C>T (p.Pro131Ser)not specified [RCV004256520]uncertain significance3183154050183154050Humanname
401738575CV2676324single nucleotide variantNM_014398.4(LAMP3):c.726G>A (p.Met242Ile)not specified [RCV004286358]uncertain significance3183153715183153715Humanname
401718882CV2679338single nucleotide variantNM_014398.4(LAMP3):c.476C>A (p.Thr159Asn)not specified [RCV004285877]uncertain significance3183153965183153965Humanname
401749757CV2694738single nucleotide variantNM_014398.4(LAMP3):c.950C>T (p.Thr317Ile)not specified [RCV004298825]uncertain significance3183135884183135884Humanname
401861246CV2755497single nucleotide variantNM_014398.4(LAMP3):c.840C>A (p.Asn280Lys)not specified [RCV004340081]uncertain significance3183152423183152423Humanname
401893091CV2762860single nucleotide variantNM_014398.4(LAMP3):c.544G>A (p.Gly182Ser)not specified [RCV004340406]likely benign3183153897183153897Humanname
401864234CV2781606single nucleotide variantNM_014398.4(LAMP3):c.922G>A (p.Ala308Thr)not specified [RCV004354815]uncertain significance3183140562183140562Humanname
401919457CV2794627single nucleotide variantNM_014398.4(LAMP3):c.862G>A (p.Gly288Arg)See cases [RCV003388301]|not specified [RCV004935323]uncertain significance3183152401183152401Humanname
405814885CV3273072single nucleotide variantNM_014398.4(LAMP3):c.317C>T (p.Thr106Ile)not specified [RCV004410061]uncertain significance3183154124183154124Humanname
405814887CV3273073single nucleotide variantNM_014398.4(LAMP3):c.394T>G (p.Tyr132Asp)not specified [RCV004410062]uncertain significance3183154047183154047Humanname
405814891CV3273075single nucleotide variantNM_014398.4(LAMP3):c.747A>C (p.Gln249His)not specified [RCV004410064]uncertain significance3183153694183153694Humanname
405814893CV3273076single nucleotide variantNM_014398.4(LAMP3):c.787A>G (p.Ile263Val)not specified [RCV004410065]uncertain significance3183152476183152476Humanname
405814895CV3273077single nucleotide variantNM_014398.4(LAMP3):c.808G>A (p.Ala270Thr)not specified [RCV004410066]uncertain significance3183152455183152455Humanname
407481823CV3456271single nucleotide variantNM_014398.4(LAMP3):c.803C>G (p.Thr268Arg)not specified [RCV004640024]uncertain significance3183152460183152460Humanname
597631311CV3701439single nucleotide variantNM_014398.4(LAMP3):c.310C>A (p.Leu104Met)not specified [RCV004939699]uncertain significance3183154131183154131Humanname
597631314CV3701440single nucleotide variantNM_014398.4(LAMP3):c.391C>G (p.Pro131Ala)not specified [RCV004939700]uncertain significance3183154050183154050Humanname
597631318CV3701441single nucleotide variantNM_014398.4(LAMP3):c.772C>T (p.Arg258Trp)not specified [RCV004939701]uncertain significance3183152491183152491Humanname
597631321CV3701442single nucleotide variantNM_014398.4(LAMP3):c.653C>T (p.Pro218Leu)not specified [RCV004939702]uncertain significance3183153788183153788Humanname
597631323CV3701443single nucleotide variantNM_014398.4(LAMP3):c.320C>T (p.Thr107Ile)not specified [RCV004939703]uncertain significance3183154121183154121Humanname
598197482CV3987579single nucleotide variantNM_014398.4(LAMP3):c.992C>T (p.Thr331Ile)not specified [RCV005355366]uncertain significance3183135842183135842Humanname
598229452CV3987580single nucleotide variantNM_014398.4(LAMP3):c.697G>A (p.Gly233Arg)not specified [RCV005362542]uncertain significance3183153744183153744Humanname
598174300CV3987582single nucleotide variantNM_014398.4(LAMP3):c.389C>A (p.Ala130Asp)not specified [RCV005371101]uncertain significance3183154052183154052Humanname
155904878CV2349603single nucleotide variantNM_014398.4(LAMP3):c.1018G>A (p.Val340Met)not specified [RCV004204027]uncertain significance3183135816183135816Humanname
329364972CV2439958single nucleotide variantNM_014398.4(LAMP3):c.1000G>A (p.Gly334Arg)not specified [RCV004260439]uncertain significance3183135834183135834Humanname
401869928CV2792224single nucleotide variantNM_014398.4(LAMP3):c.1168A>G (p.Ile390Val)not specified [RCV004361425]uncertain significance3183124164183124164Humanname
405814876CV3273068single nucleotide variantNM_014398.4(LAMP3):c.1191G>T (p.Met397Ile)not specified [RCV004410057]uncertain significance3183124141183124141Humanname
13528675CV513533deletionNM_014398.4(LAMP3):c.1172_1173del (p.Val391fs)not provided [RCV000626078]uncertain significance3183124159183124160Humanname