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Variants search result for Homo sapiens
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10 records found for search term Efcab9
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405769415CV3241600single nucleotide variantNM_001171183.2(EFCAB9):c.94T>C (p.Tyr32His)not specified [RCV004384865]uncertain significance5172194266172194266Humanname
156176265CV2317415single nucleotide variantNM_001171183.2(EFCAB9):c.280C>G (p.His94Asp)not specified [RCV004172387]uncertain significance5172199526172199526Humanname
329357614CV2453679single nucleotide variantNM_001171183.2(EFCAB9):c.210G>A (p.Met70Ile)not specified [RCV004269332]uncertain significance5172199456172199456Humanname
597645806CV3664248single nucleotide variantNM_001171183.2(EFCAB9):c.223G>C (p.Ala75Pro)not specified [RCV004909842]uncertain significance5172199469172199469Humanname
597645812CV3664249single nucleotide variantNM_001171183.2(EFCAB9):c.230G>A (p.Gly77Asp)not specified [RCV004909843]uncertain significance5172199476172199476Humanname
156312689CV2196406single nucleotide variantNM_001171183.2(EFCAB9):c.323G>A (p.Arg108Gln)not specified [RCV004073710]uncertain significance5172200603172200603Humanname
156183934CV2292196single nucleotide variantNM_001171183.2(EFCAB9):c.463C>T (p.Arg155Cys)not specified [RCV004148245]uncertain significance5172203214172203214Humanname
401758140CV2682195single nucleotide variantNM_001171183.2(EFCAB9):c.436C>T (p.Arg146Cys)not specified [RCV004290239]uncertain significance5172200716172200716Humanname
401730040CV2700386single nucleotide variantNM_001171183.2(EFCAB9):c.308T>C (p.Met103Thr)not specified [RCV004311035]uncertain significance5172200588172200588Humanname
405769409CV3241599single nucleotide variantNM_001171183.2(EFCAB9):c.514T>A (p.Leu172Ile)not specified [RCV004384864]uncertain significance5172203265172203265Humanname