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Pathways
Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)


5 records found for search term Vsnl1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405663571CV3342324single nucleotide variantNM_003385.5(VSNL1):c.8A>G (p.Lys3Arg)not specified [RCV004485020]uncertain significance21759208217592082Humanname
401734910CV2737119deletionNM_003385.5(VSNL1):c.-5-10102_-5-7979delSee cases [RCV003313911]uncertain significance21758196617584089Humanname
405663568CV3342323single nucleotide variantNM_003385.5(VSNL1):c.187A>G (p.Lys63Glu)not specified [RCV004485019]uncertain significance21764943417649434Humanname
598256021CV3926159single nucleotide variantNM_003385.5(VSNL1):c.281G>A (p.Arg94Lys)not specified [RCV005299536]uncertain significance21764952817649528Humanname
401737863CV2703678single nucleotide variantNM_003385.5(VSNL1):c.353G>A (p.Arg118Gln)not specified [RCV004315929]uncertain significance21764960017649600Humanname