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Variants search result for Homo sapiens
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31 records found for search term Efnb3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401721549CV2683554single nucleotide variantNM_001406.4(EFNB3):c.8C>T (p.Pro3Leu)not specified [RCV004282486]uncertain significance1777056067705606Humanname
407497886CV3441778single nucleotide variantNM_001406.4(EFNB3):c.5G>A (p.Gly2Glu)not specified [RCV004622325]uncertain significance1777056037705603Humanname
156057559CV2383213single nucleotide variantNM_001406.4(EFNB3):c.26G>A (p.Gly9Glu)not specified [RCV004220223]uncertain significance1777056247705624Humanname
329372220CV2443063single nucleotide variantNM_001406.4(EFNB3):c.13C>T (p.His5Tyr)not specified [RCV004253650]uncertain significance1777056117705611Humanname
329399423CV2470091single nucleotide variantNM_001406.4(EFNB3):c.40G>A (p.Gly14Arg)not specified [RCV004287353]uncertain significance1777056387705638Humanname
405716012CV3241670single nucleotide variantNM_001406.4(EFNB3):c.29G>C (p.Gly10Ala)not specified [RCV004377407]uncertain significance1777056277705627Humanname
156049284CV2391076single nucleotide variantNM_001406.4(EFNB3):c.272G>T (p.Arg91Leu)not specified [RCV004235067]uncertain significance1777081077708107Humanname
598167529CV3964889single nucleotide variantNM_001406.4(EFNB3):c.193G>A (p.Ala65Thr)not specified [RCV005330065]uncertain significance1777080287708028Humanname
598167536CV3964890single nucleotide variantNM_001406.4(EFNB3):c.289G>T (p.Ala97Ser)not specified [RCV005330066]uncertain significance1777081247708124Humanname
156399890CV2202286single nucleotide variantNM_001406.4(EFNB3):c.389G>A (p.Arg130His)not specified [RCV004078218]uncertain significance1777082247708224Humanname
156236665CV2206689single nucleotide variantNM_001406.4(EFNB3):c.388C>T (p.Arg130Cys)not specified [RCV004083383]uncertain significance1777082237708223Humanname
155931726CV2221085single nucleotide variantNM_001406.4(EFNB3):c.515G>A (p.Arg172Gln)not specified [RCV004094540]uncertain significance1777086417708641Humanname
156386105CV2228118single nucleotide variantNM_001406.4(EFNB3):c.620C>T (p.Pro207Leu)not specified [RCV004096341]uncertain significance1777091737709173Humanname
155969019CV2244400single nucleotide variantNM_001406.4(EFNB3):c.983G>T (p.Gly328Val)not specified [RCV004100372]uncertain significance1777095367709536Humanname
156344002CV2364207single nucleotide variantNM_001406.4(EFNB3):c.901G>A (p.Gly301Arg)not specified [RCV004223444]uncertain significance1777094547709454Humanname
405716018CV3241671single nucleotide variantNM_001406.4(EFNB3):c.781A>G (p.Ser261Gly)not specified [RCV004377408]uncertain significance1777093347709334Humanname
405716027CV3241672single nucleotide variantNM_001406.4(EFNB3):c.842G>A (p.Gly281Asp)not specified [RCV004377409]uncertain significance1777093957709395Humanname
405716034CV3241673single nucleotide variantNM_001406.4(EFNB3):c.857G>A (p.Arg286Gln)not specified [RCV004377410]uncertain significance1777094107709410Humanname
405716041CV3241674single nucleotide variantNM_001406.4(EFNB3):c.940G>T (p.Val314Leu)not specified [RCV004377411]uncertain significance1777094937709493Humanname
407497879CV3441776single nucleotide variantNM_001406.4(EFNB3):c.724G>A (p.Val242Met)not specified [RCV004622323]uncertain significance1777092777709277Humanname
407497882CV3441777single nucleotide variantNM_001406.4(EFNB3):c.536A>T (p.Lys179Ile)not specified [RCV004622324]uncertain significance1777086627708662Humanname
407497890CV3441779single nucleotide variantNM_001406.4(EFNB3):c.421T>G (p.Ser141Ala)not specified [RCV004622326]uncertain significance1777084407708440Humanname
407497895CV3441780single nucleotide variantNM_001406.4(EFNB3):c.986C>T (p.Pro329Leu)not specified [RCV004622327]uncertain significance1777095397709539Humanname
597646411CV3664349single nucleotide variantNM_001406.4(EFNB3):c.776C>T (p.Ser259Leu)not specified [RCV004909904]uncertain significance1777093297709329Humanname
597646033CV3664351single nucleotide variantNM_001406.4(EFNB3):c.664C>A (p.Pro222Thr)not specified [RCV004909906]uncertain significance1777092177709217Humanname
597646039CV3664352single nucleotide variantNM_001406.4(EFNB3):c.434G>A (p.Arg145Gln)not specified [RCV004909907]uncertain significance1777084537708453Humanname
597736533CV3664353single nucleotide variantNM_001406.4(EFNB3):c.641G>A (p.Arg214Gln)not specified [RCV004920653]uncertain significance1777091947709194Humanname
597646046CV3664354single nucleotide variantNM_001406.4(EFNB3):c.926C>T (p.Pro309Leu)not specified [RCV004909908]uncertain significance1777094797709479Humanname
597646054CV3664355single nucleotide variantNM_001406.4(EFNB3):c.959A>G (p.His320Arg)not specified [RCV004909909]uncertain significance1777095127709512Humanname
598167541CV3964891single nucleotide variantNM_001406.4(EFNB3):c.616G>A (p.Asp206Asn)not specified [RCV005330067]uncertain significance1777091697709169Humanname
15188337CV727462single nucleotide variantNM_001406.4(EFNB3):c.521G>C (p.Gly174Ala)not provided [RCV000887504]benign1777086477708647Humanname