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23 records found for search term Ebpl
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8582866CV117422single nucleotide variantNM_001278636.1(EBPL):c.381-549A>GLung cancer [RCV000097943]uncertain significance134966247649662476Humanname
401742602CV2715272single nucleotide variantNM_032565.5(EBPL):c.79G>A (p.Ala27Thr)not specified [RCV004324613]uncertain significance134969134649691346Humanname
407478299CV3441444single nucleotide variantNM_032565.5(EBPL):c.68C>A (p.Ala23Glu)not specified [RCV004617492]uncertain significance134969135749691357Humanname
329392156CV2470430single nucleotide variantNM_032565.5(EBPL):c.107A>G (p.Gln36Arg)not specified [RCV004273461]likely benign134969131849691318Humanname
401746037CV2694779single nucleotide variantNM_032565.5(EBPL):c.124G>T (p.Gly42Trp)not specified [RCV004298862]uncertain significance134969130149691301Humanname
401893062CV2762796single nucleotide variantNM_032565.5(EBPL):c.130C>T (p.Leu44Phe)not specified [RCV004340348]uncertain significance134969129549691295Humanname
405752895CV3238384single nucleotide variantNM_032565.5(EBPL):c.266C>T (p.Ala89Val)not specified [RCV004382260]uncertain significance134966317149663171Humanname
597803026CV3667206single nucleotide variantNM_032565.5(EBPL):c.262G>A (p.Asp88Asn)not specified [RCV004907002]uncertain significance134966317549663175Humanname
598268809CV3953938single nucleotide variantNM_032565.5(EBPL):c.208G>A (p.Val70Ile)not specified [RCV005327179]likely benign134966981049669810Humanname
156328127CV2217418single nucleotide variantNM_032565.5(EBPL):c.319G>A (p.Ala107Thr)not specified [RCV004087847]uncertain significance134966311849663118Humanname
156155671CV2328807single nucleotide variantNM_032565.5(EBPL):c.529G>T (p.Val177Phe)not specified [RCV004178030]uncertain significance134966106049661060Humanname
156155539CV2359737single nucleotide variantNM_032565.5(EBPL):c.319G>T (p.Ala107Ser)not specified [RCV004210554]uncertain significance134966311849663118Humanname
401869559CV2772443single nucleotide variantNM_032565.5(EBPL):c.412G>C (p.Glu138Gln)not specified [RCV004355229]uncertain significance134966117749661177Humanname
405752902CV3238385single nucleotide variantNM_032565.5(EBPL):c.359T>C (p.Ile120Thr)not specified [RCV004382261]uncertain significance134966307849663078Humanname
405752912CV3238386single nucleotide variantNM_032565.5(EBPL):c.467A>G (p.Asn156Ser)not specified [RCV004382262]uncertain significance134966112249661122Humanname
405752917CV3238387single nucleotide variantNM_032565.5(EBPL):c.526T>A (p.Trp176Arg)not specified [RCV004382263]uncertain significance134966106349661063Humanname
407478294CV3441443single nucleotide variantNM_032565.5(EBPL):c.379C>T (p.Arg127Trp)not specified [RCV004617491]uncertain significance134966305849663058Humanname
407478304CV3441445single nucleotide variantNM_032565.5(EBPL):c.406G>A (p.Val136Met)not specified [RCV004617493]uncertain significance134966118349661183Humanname
407478309CV3441446single nucleotide variantNM_032565.5(EBPL):c.412G>A (p.Glu138Lys)not specified [RCV004617494]uncertain significance134966117749661177Humanname
407478316CV3441447single nucleotide variantNM_032565.5(EBPL):c.326A>G (p.Asp109Gly)not specified [RCV004617495]uncertain significance134966311149663111Humanname
597803024CV3667205single nucleotide variantNM_032565.5(EBPL):c.538C>T (p.Pro180Ser)not specified [RCV004907001]uncertain significance134966105149661051Humanname
597803027CV3667207single nucleotide variantNM_032565.5(EBPL):c.482A>G (p.Asn161Ser)not specified [RCV004907003]likely benign134966110749661107Humanname
597735758CV3667208single nucleotide variantNM_032565.5(EBPL):c.548T>G (p.Leu183Arg)not specified [RCV004920529]uncertain significance134966104149661041Humanname