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13 records found for search term Lce1c
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598175022CV3987814single nucleotide variantNM_178351.4(LCE1C):c.17G>A (p.Ser6Asn)not specified [RCV005371208]likely benign1152805462152805462Humanname
401891977CV2777178single nucleotide variantNM_178351.4(LCE1C):c.34C>A (p.Pro12Thr)not specified [RCV004354218]uncertain significance1152805445152805445Humanname
156398878CV2194842single nucleotide variantNM_178351.4(LCE1C):c.113C>T (p.Pro38Leu)not specified [RCV004075379]uncertain significance1152805366152805366Humanname
405817482CV3283758single nucleotide variantNM_178351.4(LCE1C):c.259T>C (p.Cys87Arg)not specified [RCV004412416]likely benign1152805220152805220Humanname
407491215CV3452484single nucleotide variantNM_178351.4(LCE1C):c.107A>G (p.Lys36Arg)not specified [RCV004642167]uncertain significance1152805372152805372Humanname
407491220CV3452485single nucleotide variantNM_178351.4(LCE1C):c.187A>G (p.Ser63Gly)not specified [RCV004642168]uncertain significance1152805292152805292Humanname
597631908CV3698703single nucleotide variantNM_178351.4(LCE1C):c.232A>C (p.Ser78Arg)not specified [RCV004939892]uncertain significance1152805247152805247Humanname
597631912CV3698704single nucleotide variantNM_178351.4(LCE1C):c.218G>T (p.Gly73Val)not specified [RCV004939893]uncertain significance1152805261152805261Humanname
598175007CV3987812single nucleotide variantNM_178351.4(LCE1C):c.211G>C (p.Gly71Arg)not specified [RCV005371206]uncertain significance1152805268152805268Humanname
598175014CV3987813single nucleotide variantNM_178351.4(LCE1C):c.244C>T (p.Arg82Cys)not specified [RCV005371207]uncertain significance1152805235152805235Humanname
15193020CV696106single nucleotide variantNM_178351.4(LCE1C):c.200G>T (p.Cys67Phe)not provided [RCV000955248]benign1152805279152805279Humanname
329392596CV2471349single nucleotide variantNM_178351.4(LCE1C):c.305G>T (p.Gly102Val)not specified [RCV004280357]uncertain significance1152805174152805174Humanname
15157982CV706702single nucleotide variantNM_178351.4(LCE1C):c.317G>A (p.Cys106Tyr)not provided [RCV000969414]benign1152805162152805162Humanname