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Variants search result for Homo sapiens
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42 records found for search term Scrn1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
150456796CV1248701single nucleotide variantNM_014766.5(SCRN1):c.*639G>Anot provided [RCV001668877]benign72992331829923318Humanname
155928031CV2349930single nucleotide variantNM_014766.5(SCRN1):c.47G>A (p.Arg16His)not specified [RCV004206343]uncertain significance72996902129969021Humanname
407461841CV3480233single nucleotide variantNM_014766.5(SCRN1):c.58G>C (p.Gly20Arg)not specified [RCV004658859]uncertain significance72996901029969010Humanname
597693153CV3598375single nucleotide variantNM_014766.5(SCRN1):c.37T>C (p.Phe13Leu)not specified [RCV004859079]uncertain significance72996903129969031Humanname
156370961CV2204390single nucleotide variantNM_014766.5(SCRN1):c.169A>G (p.Ile57Val)not specified [RCV004079206]uncertain significance72995535129955351Humanname
10767091CV221010single nucleotide variantNM_014766.5(SCRN1):c.178G>A (p.Asp60Asn)Prostate cancer [RCV000204152]uncertain significance72995534229955342Human2name
156177668CV2355872single nucleotide variantNM_014766.5(SCRN1):c.271G>T (p.Ala91Ser)not specified [RCV004201262]uncertain significance72995524929955249Humanname
401776750CV2711331single nucleotide variantNM_014766.5(SCRN1):c.119A>G (p.Tyr40Cys)not specified [RCV004313101]uncertain significance72996894929968949Humanname
401879716CV2755242single nucleotide variantNM_014766.5(SCRN1):c.131C>T (p.Ala44Val)not specified [RCV004337425]uncertain significance72996893729968937Humanname
405759680CV3314064single nucleotide variantNM_014766.5(SCRN1):c.204A>G (p.Ile68Met)not specified [RCV004455079]uncertain significance72995531629955316Humanname
597693099CV3598369single nucleotide variantNM_014766.5(SCRN1):c.175A>G (p.Ile59Val)not specified [RCV004859074]uncertain significance72995534529955345Humanname
597693143CV3598374single nucleotide variantNM_014766.5(SCRN1):c.274A>G (p.Asn92Asp)not specified [RCV004859078]uncertain significance72995524629955246Humanname
597693161CV3598376single nucleotide variantNM_014766.5(SCRN1):c.143C>A (p.Pro48Gln)not specified [RCV004859080]likely benign72996892529968925Humanname
598235748CV3910605single nucleotide variantNM_014766.5(SCRN1):c.297G>T (p.Glu99Asp)not specified [RCV005275293]uncertain significance72995522329955223Humanname
156318163CV2200261single nucleotide variantNM_014766.5(SCRN1):c.508A>G (p.Thr170Ala)not specified [RCV004076603]uncertain significance72994401329944013Humanname
156230835CV2235099single nucleotide variantNM_014766.5(SCRN1):c.848C>T (p.Pro283Leu)not specified [RCV004113275]uncertain significance72993661329936613Humanname
155949203CV2242650single nucleotide variantNM_014766.5(SCRN1):c.513A>G (p.Ile171Met)not specified [RCV004113705]uncertain significance72994400829944008Humanname
156205939CV2249914single nucleotide variantNM_014766.5(SCRN1):c.651G>C (p.Glu217Asp)not specified [RCV004122886]uncertain significance72994077029940770Humanname
156209231CV2250192single nucleotide variantNM_014766.5(SCRN1):c.484C>T (p.Arg162Cys)not specified [RCV004116989]uncertain significance72994403729944037Humanname
155950528CV2301949single nucleotide variantNM_014766.5(SCRN1):c.876C>G (p.His292Gln)not specified [RCV004156724]uncertain significance72993658529936585Humanname
156349119CV2309268single nucleotide variantNM_014766.5(SCRN1):c.782A>C (p.Lys261Thr)not specified [RCV004165432]uncertain significance72993667929936679Humanname
156224105CV2395080single nucleotide variantNM_014766.5(SCRN1):c.485G>A (p.Arg162His)not specified [RCV004236763]uncertain significance72994403629944036Humanname
156105583CV2400381single nucleotide variantNM_014766.5(SCRN1):c.925A>G (p.Ile309Val)not specified [RCV004244432]uncertain significance72992661329926613Human1name
156105583CV2400381single nucleotide variantNM_014766.5(SCRN1):c.925A>G (p.Ile309Val)not specified [RCV004244432]uncertain significance72992661329926614Human1name
401782185CV2719217single nucleotide variantNM_014766.5(SCRN1):c.863C>A (p.Ser288Tyr)not specified [RCV004324870]uncertain significance72993659829936598Humanname
401863546CV2776973single nucleotide variantNM_014766.5(SCRN1):c.641G>C (p.Trp214Ser)not specified [RCV004351783]uncertain significance72994078029940780Humanname
405759687CV3314065single nucleotide variantNM_014766.5(SCRN1):c.655G>A (p.Glu219Lys)not specified [RCV004455080]uncertain significance72994076629940766Humanname
405759694CV3314066single nucleotide variantNM_014766.5(SCRN1):c.707G>A (p.Gly236Asp)not specified [RCV004455081]uncertain significance72994071429940714Humanname
405759698CV3314067single nucleotide variantNM_014766.5(SCRN1):c.742A>G (p.Ser248Gly)not specified [RCV004455082]uncertain significance72993671929936719Humanname
407461845CV3480234single nucleotide variantNM_014766.5(SCRN1):c.745A>G (p.Ile249Val)not specified [RCV004658860]uncertain significance72993671629936716Humanname
597693169CV3594919single nucleotide variantNM_014766.5(SCRN1):c.674T>C (p.Val225Ala)not specified [RCV004859081]uncertain significance72994074729940747Humanname
597693090CV3598368single nucleotide variantNM_014766.5(SCRN1):c.375A>T (p.Glu125Asp)not specified [RCV004859073]uncertain significance72994414629944146Humanname
597693109CV3598371single nucleotide variantNM_014766.5(SCRN1):c.618T>G (p.Ser206Arg)not specified [RCV004859075]uncertain significance72994080329940803Humanname
598235733CV3910603single nucleotide variantNM_014766.5(SCRN1):c.818T>A (p.Leu273His)not specified [RCV005275291]uncertain significance72993664329936643Humanname
9686854CV171434single nucleotide variantNM_014766.5(SCRN1):c.1223C>T (p.Thr408Met)Prostate cancer [RCV000149072]uncertain significance72992397929923979Human2name
156228815CV2199433single nucleotide variantNM_014766.5(SCRN1):c.1069A>G (p.Ile357Val)not specified [RCV004070995]likely benign72992646929926469Humanname
329372178CV2455079single nucleotide variantNM_014766.5(SCRN1):c.1182C>G (p.Asp394Glu)not specified [RCV004272328]uncertain significance72992402029924020Humanname
405759676CV3314063single nucleotide variantNM_014766.5(SCRN1):c.1208A>G (p.Tyr403Cys)not specified [RCV004455078]uncertain significance72992399429923994Humanname
597693180CV3594920single nucleotide variantNM_014766.5(SCRN1):c.1006C>G (p.Arg336Gly)not specified [RCV004859082]uncertain significance72992653229926532Humanname
597693121CV3598372single nucleotide variantNM_014766.5(SCRN1):c.1178T>C (p.Leu393Pro)not specified [RCV004859076]likely benign72992402429924024Humanname
597693134CV3598373single nucleotide variantNM_014766.5(SCRN1):c.1196G>C (p.Gly399Ala)not specified [RCV004859077]uncertain significance72992400629924006Humanname
598235742CV3910604single nucleotide variantNM_014766.5(SCRN1):c.1054G>A (p.Glu352Lys)not specified [RCV005275292]uncertain significance72992648429926484Humanname