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19 records found for search term Morf4l1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155972487CV2309414single nucleotide variantNM_006791.4(MORF4L1):c.156-1163G>Cnot specified [RCV004165558]uncertain significance157888497878884978Humanname
155964417CV2330442single nucleotide variantNM_006791.4(MORF4L1):c.156-1100C>Gnot specified [RCV004181015]uncertain significance157888504178885041Humanname
401775119CV2713785single nucleotide variantNM_006791.4(MORF4L1):c.156-1143T>Anot specified [RCV004321128]likely benign157888499878884998Humanname
405706047CV3362148single nucleotide variantNM_006791.4(MORF4L1):c.156-1155C>Tnot specified [RCV004493136]uncertain significance157888498678884986Humanname
405706106CV3362156single nucleotide variantNM_006791.4(MORF4L1):c.156-1074C>Anot specified [RCV004493144]uncertain significance157888506778885067Humanname
597660374CV3563903single nucleotide variantNM_006791.4(MORF4L1):c.156-1167G>Tnot specified [RCV004828369]uncertain significance157888497478884974Humanname
598167970CV3986289single nucleotide variantNM_006791.4(MORF4L1):c.156-1064C>Tnot specified [RCV005369618]uncertain significance157888507778885077Humanname
598201203CV3986290single nucleotide variantNM_006791.4(MORF4L1):c.156-1154G>Anot specified [RCV005375987]uncertain significance157888498778884987Humanname
8584582CV119156single nucleotide variantNM_001265603.1(MORF4L1):c.-109-3526A>GLung cancer [RCV000099676]uncertain significance157888261578882615Humanname
401749050CV2713611single nucleotide variantNM_006791.4(MORF4L1):c.28A>G (p.Lys10Glu)not specified [RCV004320986]uncertain significance157887304578873045Humanname
405706140CV3362161single nucleotide variantNM_006791.4(MORF4L1):c.197T>C (p.Val66Ala)not specified [RCV004493149]uncertain significance157888618278886182Humanname
407495973CV3453876single nucleotide variantNM_006791.4(MORF4L1):c.173C>T (p.Pro58Leu)not specified [RCV004643349]uncertain significance157888615878886158Humanname
598201210CV3986291single nucleotide variantNM_006791.4(MORF4L1):c.103A>G (p.Ile35Val)not specified [RCV005375988]uncertain significance157888052778880527Humanname
156205400CV2311356single nucleotide variantNM_006791.4(MORF4L1):c.379A>G (p.Ser127Gly)not specified [RCV004166422]uncertain significance157889151378891513Humanname
156194026CV2351906single nucleotide variantNM_006791.4(MORF4L1):c.866A>G (p.Asn289Ser)not specified [RCV004198047]uncertain significance157889488378894883Humanname
156051953CV2363300single nucleotide variantNM_006791.4(MORF4L1):c.368G>C (p.Gly123Ala)not specified [RCV004213852]uncertain significance157889150278891502Humanname
401869602CV2772458single nucleotide variantNM_006791.4(MORF4L1):c.902A>G (p.Asn301Ser)not specified [RCV004355240]uncertain significance157889699778896997Humanname
407495969CV3453875single nucleotide variantNM_006791.4(MORF4L1):c.452T>C (p.Met151Thr)not specified [RCV004643348]uncertain significance157889222578892225Humanname
597660368CV3563902single nucleotide variantNM_006791.4(MORF4L1):c.610C>T (p.Arg204Cys)not specified [RCV004828368]uncertain significance157889360878893608Humanname