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32 records found for search term Lrrc55
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156224755CV2202997single nucleotide variantNM_001005210.4(LRRC55):c.-60G>Anot specified [RCV004069252]uncertain significance115718196357181963Humanname
156270933CV2286248single nucleotide variantNM_001005210.4(LRRC55):c.-36G>Anot specified [RCV004146208]uncertain significance115718198757181987Humanname
597632892CV3693504single nucleotide variantNM_001005210.4(LRRC55):c.-42C>Tnot specified [RCV004940143]uncertain significance115718198157181981Humanname
401857815CV2769607single nucleotide variantNM_001005210.2(LRRC55):c.13C>T (p.Pro5Ser)not specified [RCV004351251]likely benign115718190657181906Humanname
329366560CV2441709single nucleotide variantNM_001005210.4(LRRC55):c.54G>A (p.Met18Ile)not specified [RCV004259878]uncertain significance115718207657182076Humanname
401768803CV2716735single nucleotide variantNM_001005210.4(LRRC55):c.67C>T (p.Leu23Phe)not specified [RCV004327779]uncertain significance115718208957182089Humanname
598222607CV3984762single nucleotide variantNM_001005210.4(LRRC55):c.95C>T (p.Ser32Leu)not specified [RCV005379915]uncertain significance115718211757182117Humanname
156078999CV2198349single nucleotide variantNM_001005210.4(LRRC55):c.133C>T (p.Arg45Cys)not specified [RCV004081892]uncertain significance115718215557182155Humanname
156028848CV2205867single nucleotide variantNM_001005210.4(LRRC55):c.278T>G (p.Val93Gly)not specified [RCV004078306]uncertain significance115718230057182300Humanname
156141453CV2243828single nucleotide variantNM_001005210.4(LRRC55):c.171C>G (p.Phe57Leu)not specified [RCV004114781]uncertain significance115718219357182193Humanname
329367775CV2427553single nucleotide variantNM_001005210.4(LRRC55):c.227G>A (p.Arg76His)not specified [RCV004250190]uncertain significance115718224957182249Humanname
405656064CV3287896single nucleotide variantNM_001005210.4(LRRC55):c.118G>A (p.Val40Ile)not specified [RCV004415684]uncertain significance115718214057182140Humanname
407501100CV3456562single nucleotide variantNM_001005210.4(LRRC55):c.164G>A (p.Arg55Gln)not specified [RCV004644786]uncertain significance115718218657182186Humanname
407501104CV3456563single nucleotide variantNM_001005210.4(LRRC55):c.265A>G (p.Met89Val)not specified [RCV004644787]uncertain significance115718228757182287Humanname
407468190CV3456564single nucleotide variantNM_001005210.4(LRRC55):c.175G>A (p.Val59Met)not specified [RCV004636185]uncertain significance115718219757182197Humanname
407468193CV3456566single nucleotide variantNM_001005210.4(LRRC55):c.143T>G (p.Val48Gly)not specified [RCV004636186]uncertain significance115718216557182165Humanname
597632903CV3693507single nucleotide variantNM_001005210.4(LRRC55):c.245C>T (p.Pro82Leu)not specified [RCV004940145]uncertain significance115718226757182267Humanname
597632907CV3693508single nucleotide variantNM_001005210.4(LRRC55):c.111C>G (p.Ser37Arg)not specified [RCV004940146]uncertain significance115718213357182133Humanname
155941479CV2229162single nucleotide variantNM_001005210.4(LRRC55):c.316C>T (p.Arg106Trp)not specified [RCV004099203]uncertain significance115718233857182338Humanname
155947471CV2234819single nucleotide variantNM_001005210.4(LRRC55):c.351C>G (p.His117Gln)not specified [RCV004113046]uncertain significance115718237357182373Humanname
156152427CV2318906single nucleotide variantNM_001005210.4(LRRC55):c.455G>C (p.Arg152Thr)not specified [RCV004175804]uncertain significance115718247757182477Humanname
156102890CV2352325single nucleotide variantNM_001005210.4(LRRC55):c.700G>A (p.Glu234Lys)not specified [RCV004200799]uncertain significance115718728357187283Humanname
329357751CV2427825single nucleotide variantNM_001005210.4(LRRC55):c.685G>A (p.Gly229Ser)not specified [RCV004252600]uncertain significance115718726857187268Humanname
329399575CV2443282single nucleotide variantNM_001005210.4(LRRC55):c.889G>A (p.Glu297Lys)not specified [RCV004260084]uncertain significance115718747257187472Humanname
401889699CV2766842single nucleotide variantNM_001005210.4(LRRC55):c.787T>A (p.Phe263Ile)not specified [RCV004349227]uncertain significance115718737057187370Humanname
405656066CV3287897single nucleotide variantNM_001005210.4(LRRC55):c.742G>T (p.Ala248Ser)not specified [RCV004415685]uncertain significance115718732557187325Humanname
405656067CV3287898single nucleotide variantNM_001005210.4(LRRC55):c.799G>A (p.Val267Met)not specified [RCV004415686]uncertain significance115718738257187382Humanname
407501108CV3456565single nucleotide variantNM_001005210.4(LRRC55):c.443C>T (p.Pro148Leu)not specified [RCV004644788]uncertain significance115718246557182465Humanname
597632887CV3693503single nucleotide variantNM_001005210.4(LRRC55):c.710C>T (p.Pro237Leu)not specified [RCV004940142]uncertain significance115718729357187293Humanname
597632898CV3693505single nucleotide variantNM_001005210.4(LRRC55):c.580G>A (p.Gly194Ser)not specified [RCV004940144]uncertain significance115718260257182602Humanname
598222600CV3984761single nucleotide variantNM_001005210.4(LRRC55):c.863G>A (p.Arg288His)not specified [RCV005379914]uncertain significance115718744657187446Humanname
598222613CV3984763single nucleotide variantNM_001005210.4(LRRC55):c.509G>A (p.Ser170Asn)not specified [RCV005379916]uncertain significance115718253157182531Humanname