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Variants search result for Homo sapiens
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36 records found for search term Samsn1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15178458CV745324single nucleotide variantNM_022136.5(SAMSN1):c.561+9A>Gnot provided [RCV000906882]benign211451030114510301Humanname
156212807CV2385809single nucleotide variantNM_022136.5(SAMSN1):c.92G>A (p.Arg31Gln)not specified [RCV004226861]uncertain significance211452118714521187Humanname
156006341CV2394148single nucleotide variantNM_022136.5(SAMSN1):c.94A>C (p.Asn32His)not specified [RCV004236346]uncertain significance211452118514521185Humanname
401779307CV2718480single nucleotide variantNM_022136.5(SAMSN1):c.91C>T (p.Arg31Trp)not specified [RCV004318291]uncertain significance211452118814521188Humanname
617149199CV4021543single nucleotide variantNM_022136.5(SAMSN1):c.537T>C (p.Tyr179=)not provided [RCV005425512]likely benign211451033414510334Humanname
156146446CV2289212single nucleotide variantNM_022136.5(SAMSN1):c.235A>G (p.Lys79Glu)not specified [RCV004152208]uncertain significance211451693614516936Humanname
156387077CV2372623single nucleotide variantNM_022136.5(SAMSN1):c.263C>A (p.Ala88Asp)not specified [RCV004221827]uncertain significance211451690814516908Humanname
597789629CV3604953single nucleotide variantNM_022136.5(SAMSN1):c.167A>G (p.Gln56Arg)not specified [RCV004855806]uncertain significance211451700414517004Humanname
597789641CV3604956single nucleotide variantNM_022136.5(SAMSN1):c.210G>A (p.Met70Ile)not specified [RCV004855809]uncertain significance211451696114516961Humanname
155975684CV2231432single nucleotide variantNM_022136.5(SAMSN1):c.689A>G (p.Lys230Arg)not specified [RCV004096511]uncertain significance211450060814500608Humanname
156281215CV2252312single nucleotide variantNM_022136.5(SAMSN1):c.834G>T (p.Glu278Asp)not specified [RCV004116170]uncertain significance211449852714498527Humanname
156111097CV2353309single nucleotide variantNM_022136.5(SAMSN1):c.484G>A (p.Gly162Arg)not specified [RCV004205778]uncertain significance211451038714510387Humanname
156384423CV2371425single nucleotide variantNM_022136.5(SAMSN1):c.499C>T (p.Arg167Cys)not specified [RCV004216688]uncertain significance211451037214510372Humanname
401779305CV2718479single nucleotide variantNM_022136.5(SAMSN1):c.358C>A (p.Leu120Ile)not specified [RCV004318290]uncertain significance211451249514512495Humanname
401769076CV2729510single nucleotide variantNM_022136.5(SAMSN1):c.650T>C (p.Ile217Thr)not specified [RCV004333596]uncertain significance211450064714500647Humanname
401890510CV2778815single nucleotide variantNM_022136.5(SAMSN1):c.610A>T (p.Thr204Ser)not specified [RCV004346713]uncertain significance211450068714500687Humanname
401865551CV2778816single nucleotide variantNM_022136.5(SAMSN1):c.611C>T (p.Thr204Ile)not specified [RCV004346714]uncertain significance211450068614500686Humanname
405722890CV3320497single nucleotide variantNM_022136.5(SAMSN1):c.332T>C (p.Ile111Thr)not specified [RCV004450058]uncertain significance211451252114512521Humanname
405722898CV3320498single nucleotide variantNM_022136.5(SAMSN1):c.683C>T (p.Ala228Val)not specified [RCV004450059]uncertain significance211450061414500614Humanname
407469300CV3483603single nucleotide variantNM_022136.5(SAMSN1):c.710G>T (p.Arg237Met)not specified [RCV004661431]uncertain significance211450058714500587Humanname
407469304CV3483604single nucleotide variantNM_022136.5(SAMSN1):c.344C>G (p.Thr115Arg)not specified [RCV004661432]uncertain significance211451250914512509Humanname
597789613CV3604949single nucleotide variantNM_022136.5(SAMSN1):c.380A>G (p.Asp127Gly)not specified [RCV004855802]uncertain significance211451247314512473Humanname
597789616CV3604950single nucleotide variantNM_022136.5(SAMSN1):c.515C>T (p.Thr172Met)not specified [RCV004855803]uncertain significance211451035614510356Humanname
597789621CV3604951single nucleotide variantNM_022136.5(SAMSN1):c.840C>G (p.His280Gln)not specified [RCV004855804]uncertain significance211449852114498521Humanname
597789625CV3604952single nucleotide variantNM_022136.5(SAMSN1):c.476C>T (p.Pro159Leu)not specified [RCV004855805]uncertain significance211451039514510395Humanname
597789647CV3604957single nucleotide variantNM_022136.5(SAMSN1):c.675G>C (p.Glu225Asp)not specified [RCV004855810]uncertain significance211450062214500622Humanname
598223097CV3903734single nucleotide variantNM_022136.5(SAMSN1):c.446G>A (p.Arg149Gln)not specified [RCV005272996]uncertain significance211451042514510425Humanname
598223103CV3903735single nucleotide variantNM_022136.5(SAMSN1):c.829A>G (p.Lys277Glu)not specified [RCV005272997]uncertain significance211449853214498532Humanname
598223122CV3903738single nucleotide variantNM_022136.5(SAMSN1):c.892G>A (p.Ala298Thr)not specified [RCV005273000]uncertain significance211449846914498469Humanname
598223127CV3903739single nucleotide variantNM_022136.5(SAMSN1):c.754A>T (p.Arg252Trp)not specified [RCV005273001]uncertain significance211450054314500543Humanname
329401338CV2442192single nucleotide variantNM_022136.5(SAMSN1):c.1072A>G (p.Asn358Asp)not specified [RCV004264687]uncertain significance211448596214485962Humanname
401719593CV2701187single nucleotide variantNM_022136.5(SAMSN1):c.1118A>T (p.Asp373Val)not specified [RCV004309763]uncertain significance211448591614485916Humanname
407514230CV3483602single nucleotide variantNM_022136.5(SAMSN1):c.1048G>A (p.Gly350Ser)not specified [RCV004674465]uncertain significance211448598614485986Humanname
598223109CV3903736single nucleotide variantNM_022136.5(SAMSN1):c.1008G>C (p.Arg336Ser)not specified [RCV005272998]uncertain significance211448602614486026Humanname
598223115CV3903737single nucleotide variantNM_022136.5(SAMSN1):c.1001G>A (p.Cys334Tyr)not specified [RCV005272999]uncertain significance211448603314486033Humanname
15201836CV728832single nucleotide variantNM_001256370.2(SAMSN1):c.123G>T (p.Lys41Asn)not provided [RCV000891306]likely benign211458227414582274Humanname