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Variants search result for Homo sapiens
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23 records found for search term Ropn1l
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401879021CV2778089single nucleotide variantNM_031916.5(ROPN1L):c.52G>A (p.Glu18Lys)not specified [RCV004348036]uncertain significance51044221910442219Humanname
401891696CV2779314single nucleotide variantNM_031916.5(ROPN1L):c.28G>T (p.Ala10Ser)not specified [RCV004350984]uncertain significance51044219510442195Humanname
155908290CV2387277single nucleotide variantNM_031916.5(ROPN1L):c.190C>A (p.Pro64Thr)not specified [RCV004238369]uncertain significance51044831810448318Humanname
329402296CV2454004single nucleotide variantNM_031916.5(ROPN1L):c.143C>A (p.Ala48Asp)not specified [RCV004271662]uncertain significance51044827110448271Humanname
405718635CV3309772single nucleotide variantNM_031916.5(ROPN1L):c.155G>C (p.Gly52Ala)not specified [RCV004449520]uncertain significance51044828310448283Humanname
405718643CV3309773single nucleotide variantNM_031916.5(ROPN1L):c.160C>G (p.Pro54Ala)not specified [RCV004449521]uncertain significance51044828810448288Humanname
407487374CV3479890single nucleotide variantNM_031916.5(ROPN1L):c.103C>A (p.Pro35Thr)not specified [RCV004665615]uncertain significance51044227010442270Humanname
598207273CV3906107single nucleotide variantNM_031916.5(ROPN1L):c.128C>T (p.Ala43Val)not specified [RCV005270017]uncertain significance51044229510442295Humanname
598207279CV3906108single nucleotide variantNM_031916.5(ROPN1L):c.177C>G (p.Asp59Glu)not specified [RCV005270018]uncertain significance51044830510448305Humanname
598207290CV3906110single nucleotide variantNM_031916.5(ROPN1L):c.274G>A (p.Val92Met)not specified [RCV005270020]uncertain significance51044997010449970Humanname
329402295CV2454005single nucleotide variantNM_031916.5(ROPN1L):c.398G>C (p.Gly133Ala)not specified [RCV004271663]uncertain significance51045009410450094Humanname
329399258CV2470013single nucleotide variantNM_031916.5(ROPN1L):c.319C>A (p.Pro107Thr)not specified [RCV004287289]uncertain significance51045001510450015Humanname
401866702CV2776511single nucleotide variantNM_031916.5(ROPN1L):c.485G>C (p.Arg162Pro)not specified [RCV004355612]uncertain significance51046125110461251Humanname
405718657CV3309774single nucleotide variantNM_031916.5(ROPN1L):c.378G>T (p.Trp126Cys)not specified [RCV004449522]uncertain significance51045007410450074Humanname
405718668CV3309775single nucleotide variantNM_031916.5(ROPN1L):c.395T>A (p.Leu132His)not specified [RCV004449523]uncertain significance51045009110450091Humanname
405718677CV3309776single nucleotide variantNM_031916.5(ROPN1L):c.511G>T (p.Val171Phe)not specified [RCV004449524]uncertain significance51046127710461277Humanname
405718684CV3309777single nucleotide variantNM_031916.5(ROPN1L):c.517C>T (p.Arg173Cys)not specified [RCV004449525]uncertain significance51046128310461283Humanname
407513554CV3479887single nucleotide variantNM_031916.5(ROPN1L):c.521A>G (p.Tyr174Cys)not specified [RCV004674168]uncertain significance51046128710461287Humanname
407487583CV3479888single nucleotide variantNM_031916.5(ROPN1L):c.431C>T (p.Ala144Val)not specified [RCV004665613]uncertain significance51046119710461197Humanname
407487488CV3479889single nucleotide variantNM_031916.5(ROPN1L):c.628G>T (p.Asp210Tyr)not specified [RCV004665614]uncertain significance51046488210464882Humanname
597756229CV3586930single nucleotide variantNM_031916.5(ROPN1L):c.312G>T (p.Leu104Phe)not specified [RCV004847717]uncertain significance51045000810450008Humanname
597689324CV3586931single nucleotide variantNM_031916.5(ROPN1L):c.566C>G (p.Ser189Cys)not specified [RCV004858692]uncertain significance51046133210461332Humanname
598207284CV3906109single nucleotide variantNM_031916.5(ROPN1L):c.647G>A (p.Arg216Lys)not specified [RCV005270019]uncertain significance51046490110464901Humanname