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Variants search result for Homo sapiens
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27 records found for search term Snrnp35
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401735035CV2688690single nucleotide variantNM_022717.4(SNRNP35):c.1A>G (p.Met1Val)not specified [RCV004301628]uncertain significance12123465541123465541Humanname
156136004CV2196135single nucleotide variantNM_022717.4(SNRNP35):c.89C>T (p.Ala30Val)not specified [RCV004073496]uncertain significance12123465629123465629Humanname
156368917CV2267112single nucleotide variantNM_022717.4(SNRNP35):c.86G>A (p.Arg29His)not specified [RCV004131731]uncertain significance12123465626123465626Humanname
401761299CV2706293single nucleotide variantNM_022717.4(SNRNP35):c.88G>A (p.Ala30Thr)not specified [RCV004314954]uncertain significance12123465628123465628Humanname
401929689CV2817050single nucleotide variantNM_022717.4(SNRNP35):c.321A>G (p.Lys107=)not provided [RCV003390340]likely benign12123465861123465861Humanname
405715243CV3326255single nucleotide variantNM_022717.4(SNRNP35):c.30G>C (p.Glu10Asp)not specified [RCV004462398]uncertain significance12123465570123465570Humanname
597744935CV3607075single nucleotide variantNM_022717.4(SNRNP35):c.47C>T (p.Ala16Val)not specified [RCV004865568]uncertain significance12123465587123465587Humanname
156227717CV2199348single nucleotide variantNM_022717.4(SNRNP35):c.221A>G (p.Tyr74Cys)not specified [RCV004070926]uncertain significance12123465761123465761Humanname
598171332CV3911578single nucleotide variantNM_022717.4(SNRNP35):c.113G>A (p.Arg38Gln)not specified [RCV005284822]uncertain significance12123465653123465653Humanname
155951774CV2238843single nucleotide variantNM_022717.4(SNRNP35):c.488G>A (p.Arg163Gln)not specified [RCV004109758]uncertain significance12123466028123466028Humanname
155924834CV2277192single nucleotide variantNM_022717.4(SNRNP35):c.508G>A (p.Val170Ile)not specified [RCV004142829]uncertain significance12123466048123466048Humanname
155965691CV2308538single nucleotide variantNM_022717.4(SNRNP35):c.482C>G (p.Pro161Arg)not specified [RCV004166815]uncertain significance12123466022123466022Humanname
329362181CV2448375single nucleotide variantNM_022717.4(SNRNP35):c.619C>T (p.Arg207Trp)not specified [RCV004256661]uncertain significance12123466159123466159Humanname
329377885CV2460805single nucleotide variantNM_022717.4(SNRNP35):c.542G>A (p.Arg181Gln)not specified [RCV004271124]uncertain significance12123466082123466082Humanname
401735876CV2672764single nucleotide variantNM_022717.4(SNRNP35):c.569G>A (p.Arg190Gln)not specified [RCV004281549]uncertain significance12123466109123466109Humanname
405715249CV3326256single nucleotide variantNM_022717.4(SNRNP35):c.527A>T (p.Tyr176Phe)not specified [RCV004462399]uncertain significance12123466067123466067Humanname
405715256CV3326257single nucleotide variantNM_022717.4(SNRNP35):c.587C>G (p.Ser196Trp)not specified [RCV004462400]uncertain significance12123466127123466127Humanname
405715264CV3326258single nucleotide variantNM_022717.4(SNRNP35):c.587C>T (p.Ser196Leu)not specified [RCV004462401]uncertain significance12123466127123466127Humanname
405715271CV3326259single nucleotide variantNM_022717.4(SNRNP35):c.647C>T (p.Pro216Leu)not specified [RCV004462402]uncertain significance12123466187123466187Humanname
405715283CV3326261single nucleotide variantNM_022717.4(SNRNP35):c.673T>G (p.Trp225Gly)not specified [RCV004462404]uncertain significance12123466213123466213Humanname
407503671CV3474647single nucleotide variantNM_022717.4(SNRNP35):c.308G>A (p.Arg103His)not specified [RCV004670334]uncertain significance12123465848123465848Humanname
407503676CV3474648single nucleotide variantNM_022717.4(SNRNP35):c.391A>G (p.Thr131Ala)not specified [RCV004670335]uncertain significance12123465931123465931Humanname
597744932CV3607074single nucleotide variantNM_022717.4(SNRNP35):c.608A>G (p.His203Arg)not specified [RCV004865567]uncertain significance12123466148123466148Humanname
598171323CV3911576single nucleotide variantNM_022717.4(SNRNP35):c.422G>C (p.Gly141Ala)not specified [RCV005284820]uncertain significance12123465962123465962Humanname
598171328CV3911577single nucleotide variantNM_022717.4(SNRNP35):c.734G>A (p.Gly245Asp)not specified [RCV005284821]uncertain significance12123466274123466274Humanname
598238419CV3911579single nucleotide variantNM_022717.4(SNRNP35):c.523C>T (p.Leu175Phe)not specified [RCV005275828]uncertain significance12123466063123466063Humanname
598171339CV3911580single nucleotide variantNM_022717.4(SNRNP35):c.665A>T (p.Asp222Val)not specified [RCV005284823]uncertain significance12123466205123466205Humanname