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28 records found for search term Lrrc52
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8575022CV109362single nucleotide variantNM_001005214.3(LRRC52):c.623-2177G>TLung cancer [RCV000089887]uncertain significance1165561328165561328Humanname
401764074CV2725424single nucleotide variantNM_001005214.4(LRRC52):c.7C>A (p.Leu3Ile)not specified [RCV004320061]uncertain significance1165544303165544303Humanname
401780106CV2676820single nucleotide variantNM_001005214.4(LRRC52):c.11C>T (p.Ala4Val)not specified [RCV004290989]uncertain significance1165544307165544307Humanname
597633145CV3693497single nucleotide variantNM_001005214.4(LRRC52):c.16G>A (p.Gly6Ser)not specified [RCV004940136]uncertain significance1165544312165544312Humanname
405656062CV3287895single nucleotide variantNM_001005214.4(LRRC52):c.62T>G (p.Val21Gly)not specified [RCV004415683]uncertain significance1165544358165544358Humanname
597633141CV3693498single nucleotide variantNM_001005214.4(LRRC52):c.67G>A (p.Gly23Arg)not specified [RCV004940137]uncertain significance1165544363165544363Humanname
598251179CV3984756single nucleotide variantNM_001005214.4(LRRC52):c.98A>G (p.Gln33Arg)not specified [RCV005366637]uncertain significance1165544394165544394Humanname
15186331CV718347single nucleotide variantNM_001005214.4(LRRC52):c.345G>C (p.Ser115=)not provided [RCV000886945]benign1165544641165544641Humanname
156253693CV2193123single nucleotide variantNM_001005214.4(LRRC52):c.136G>A (p.Glu46Lys)not specified [RCV004071126]uncertain significance1165544432165544432Humanname
156167726CV2399068single nucleotide variantNM_001005214.4(LRRC52):c.269G>A (p.Arg90Gln)not specified [RCV004245364]likely benign1165544565165544565Humanname
407501097CV3456561single nucleotide variantNM_001005214.4(LRRC52):c.112A>G (p.Ile38Val)not specified [RCV004644785]uncertain significance1165544408165544408Humanname
156262447CV2314857single nucleotide variantNM_001005214.4(LRRC52):c.889C>T (p.Arg297Trp)not specified [RCV004170976]uncertain significance1165563771165563771Humanname
156160746CV2319403single nucleotide variantNM_001005214.4(LRRC52):c.772G>A (p.Ala258Thr)not specified [RCV004184993]uncertain significance1165563654165563654Humanname
156273450CV2344131single nucleotide variantNM_001005214.4(LRRC52):c.914C>T (p.Ser305Leu)not specified [RCV004195730]uncertain significance1165563796165563796Humanname
329361191CV2459474single nucleotide variantNM_001005214.4(LRRC52):c.773C>T (p.Ala258Val)not specified [RCV004275152]uncertain significance1165563655165563655Humanname
401890413CV2768193single nucleotide variantNM_001005214.4(LRRC52):c.698G>A (p.Arg233Gln)not specified [RCV004350196]uncertain significance1165563580165563580Humanname
405656059CV3287894single nucleotide variantNM_001005214.4(LRRC52):c.316C>T (p.Leu106Phe)not specified [RCV004415682]uncertain significance1165544612165544612Humanname
407501088CV3456559single nucleotide variantNM_001005214.4(LRRC52):c.491C>G (p.Thr164Ser)not specified [RCV004644783]uncertain significance1165544787165544787Humanname
407501093CV3456560single nucleotide variantNM_001005214.4(LRRC52):c.524C>T (p.Thr175Ile)not specified [RCV004644784]uncertain significance1165544820165544820Humanname
597633149CV3693496single nucleotide variantNM_001005214.4(LRRC52):c.794T>C (p.Leu265Pro)not specified [RCV004940135]uncertain significance1165563676165563676Humanname
597632996CV3693499single nucleotide variantNM_001005214.4(LRRC52):c.703A>G (p.Met235Val)not specified [RCV004940138]uncertain significance1165563585165563585Humanname
597632872CV3693500single nucleotide variantNM_001005214.4(LRRC52):c.496G>A (p.Asp166Asn)not specified [RCV004940139]uncertain significance1165544792165544792Humanname
597632877CV3693501single nucleotide variantNM_001005214.4(LRRC52):c.368T>G (p.Val123Gly)not specified [RCV004940140]uncertain significance1165544664165544664Humanname
597632883CV3693502single nucleotide variantNM_001005214.4(LRRC52):c.320A>C (p.Asp107Ala)not specified [RCV004940141]uncertain significance1165544616165544616Humanname
598222581CV3984757single nucleotide variantNM_001005214.4(LRRC52):c.599T>C (p.Ile200Thr)not specified [RCV005379911]uncertain significance1165544895165544895Humanname
598222587CV3984758single nucleotide variantNM_001005214.4(LRRC52):c.863C>T (p.Ala288Val)not specified [RCV005379912]uncertain significance1165563745165563745Humanname
598251183CV3984759single nucleotide variantNM_001005214.4(LRRC52):c.406C>T (p.Pro136Ser)not specified [RCV005366638]uncertain significance1165544702165544702Humanname
15130752CV706827single nucleotide variantNM_001005214.4(LRRC52):c.829C>T (p.Arg277Cys)not provided [RCV000964487]benign1165563711165563711Humanname