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


9 records found for search term Snrnp27
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597740806CV3607072single nucleotide variantNM_006857.3(SNRNP27):c.38G>A (p.Arg13His)not specified [RCV004864731]uncertain significance26989509769895097Humanname
156335215CV2228360single nucleotide variantNM_006857.3(SNRNP27):c.256C>T (p.Arg86Trp)not specified [RCV004098344]uncertain significance26989653669896536Humanname
155981427CV2351327single nucleotide variantNM_006857.3(SNRNP27):c.246G>C (p.Lys82Asn)not specified [RCV004193031]uncertain significance26989652669896526Humanname
405715232CV3326253single nucleotide variantNM_006857.3(SNRNP27):c.197G>A (p.Arg66Gln)not specified [RCV004462396]uncertain significance26989647769896477Humanname
405715238CV3326254single nucleotide variantNM_006857.3(SNRNP27):c.257G>A (p.Arg86Gln)not specified [RCV004462397]uncertain significance26989653769896537Humanname
407503663CV3474645single nucleotide variantNM_006857.3(SNRNP27):c.207A>T (p.Glu69Asp)not specified [RCV004670332]uncertain significance26989648769896487Humanname
407503667CV3474646single nucleotide variantNM_006857.3(SNRNP27):c.335T>C (p.Phe112Ser)not specified [RCV004670333]uncertain significance26989744369897443Humanname
597744927CV3607073single nucleotide variantNM_006857.3(SNRNP27):c.358G>A (p.Val120Met)not specified [RCV004865566]uncertain significance26990319069903190Humanname
598171318CV3911575single nucleotide variantNM_006857.3(SNRNP27):c.370G>A (p.Val124Ile)not specified [RCV005284819]uncertain significance26990320269903202Humanname