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Variants search result for Homo sapiens
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18 records found for search term Snrpa1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597744982CV3607094single nucleotide variantNM_003090.4(SNRPA1):c.86A>G (p.Tyr29Cys)not specified [RCV004865578]uncertain significance15101293169101293169Humanname
597740861CV3607095single nucleotide variantNM_003090.4(SNRPA1):c.50A>G (p.Asn17Ser)not specified [RCV004864741]uncertain significance15101295129101295129Humanname
597740866CV3607099single nucleotide variantNM_003090.4(SNRPA1):c.97G>A (p.Val33Ile)not specified [RCV004864742]uncertain significance15101293158101293158Humanname
156146746CV2289263single nucleotide variantNM_003090.4(SNRPA1):c.268C>G (p.Leu90Val)not specified [RCV004152249]uncertain significance15101292003101292003Humanname
405731633CV3326288single nucleotide variantNM_003090.4(SNRPA1):c.201A>T (p.Lys67Asn)not specified [RCV004464412]uncertain significance15101293054101293054Humanname
407503689CV3474653single nucleotide variantNM_003090.4(SNRPA1):c.159G>C (p.Glu53Asp)not specified [RCV004670339]uncertain significance15101293096101293096Humanname
597744986CV3607096single nucleotide variantNM_003090.4(SNRPA1):c.127C>G (p.Gln43Glu)not specified [RCV004865579]uncertain significance15101293128101293128Humanname
597744990CV3607097single nucleotide variantNM_003090.4(SNRPA1):c.232C>T (p.Arg78Cys)not specified [RCV004865580]uncertain significance15101292039101292039Humanname
597744995CV3607098single nucleotide variantNM_003090.4(SNRPA1):c.173A>T (p.Asp58Val)not specified [RCV004865581]uncertain significance15101293082101293082Humanname
156382817CV2223651single nucleotide variantNM_003090.4(SNRPA1):c.700C>T (p.Arg234Cys)not specified [RCV004093775]uncertain significance15101284976101284976Humanname
156180857CV2327770single nucleotide variantNM_003090.4(SNRPA1):c.323C>G (p.Pro108Arg)not specified [RCV004179116]uncertain significance15101287689101287689Humanname
156018241CV2370248single nucleotide variantNM_003090.4(SNRPA1):c.584G>C (p.Gly195Ala)not specified [RCV004213168]uncertain significance15101285757101285757Humanname
156204597CV2385094single nucleotide variantNM_003090.4(SNRPA1):c.746A>G (p.Asp249Gly)not specified [RCV004228359]uncertain significance15101281746101281746Humanname
401858854CV2774955single nucleotide variantNM_003090.4(SNRPA1):c.301G>A (p.Val101Met)not specified [RCV004346357]uncertain significance15101291970101291970Humanname
401866504CV2782862single nucleotide variantNM_003090.4(SNRPA1):c.398T>C (p.Leu133Ser)not specified [RCV004361670]uncertain significance15101286969101286969Humanname
405731639CV3326289single nucleotide variantNM_003090.4(SNRPA1):c.698A>G (p.Glu233Gly)not specified [RCV004464413]uncertain significance15101284978101284978Humanname
597740853CV3607093single nucleotide variantNM_003090.4(SNRPA1):c.732A>T (p.Glu244Asp)not specified [RCV004864740]uncertain significance15101281760101281760Humanname
598171422CV3911597single nucleotide variantNM_003090.4(SNRPA1):c.701G>A (p.Arg234His)not specified [RCV005284838]uncertain significance15101284975101284975Humanname