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41 records found for search term Xrcc5
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
150439066CV1274897single nucleotide variantNM_021141.4(XRCC5):c.1020C>T (p.Phe340=)not provided [RCV001727972]|not specified [RCV001703249]benign|likely benign2216130957216130957Humanname
155965158CV2286885single nucleotide variantNM_021141.4(XRCC5):c.233C>T (p.Thr78Ile)not specified [RCV004142681]uncertain significance2216116756216116756Humanname
401930081CV2818903single nucleotide variantNM_021141.4(XRCC5):c.1341C>T (p.Thr447=)not provided [RCV003440154]likely benign2216138178216138178Humanname
407456142CV3493691single nucleotide variantNM_021141.4(XRCC5):c.1218C>T (p.Gly406=)not specified [RCV004685841]likely benign2216137192216137192Humanname
15193200CV697308single nucleotide variantNM_021141.4(XRCC5):c.1473T>C (p.Phe491=)not provided [RCV000955302]benign2216141316216141316Humanname
15155487CV708019single nucleotide variantNM_021141.4(XRCC5):c.2166T>C (p.Gly722=)not provided [RCV000968933]benign2216204378216204378Humanname
155916335CV2239708single nucleotide variantNM_021141.4(XRCC5):c.503C>T (p.Ser168Leu)not specified [RCV004108250]uncertain significance2216122073216122073Humanname
155984459CV2270594single nucleotide variantNM_021141.4(XRCC5):c.550C>G (p.Arg184Gly)not specified [RCV004137815]uncertain significance2216122120216122120Humanname
156091567CV2300065single nucleotide variantNM_021141.4(XRCC5):c.417C>G (p.Ser139Arg)not specified [RCV004151267]uncertain significance2216119091216119091Humanname
329397921CV2466450single nucleotide variantNM_021141.4(XRCC5):c.321C>A (p.Phe107Leu)not specified [RCV004274006]uncertain significance2216117747216117747Humanname
401766294CV2714511single nucleotide variantNM_021141.4(XRCC5):c.703T>C (p.Cys235Arg)not specified [RCV004318031]uncertain significance2216125936216125936Humanname
401865821CV2786139single nucleotide variantNM_021141.4(XRCC5):c.672T>G (p.Ile224Met)not specified [RCV004359945]uncertain significance2216122242216122242Humanname
405667023CV3349664single nucleotide variantNM_021141.4(XRCC5):c.895G>C (p.Asp299His)not specified [RCV004485691]uncertain significance2216127632216127632Humanname
597804776CV3630513single nucleotide variantNM_021141.4(XRCC5):c.563A>T (p.His188Leu)not specified [RCV004882428]uncertain significance2216122133216122133Humanname
156259877CV2204768single nucleotide variantNM_021141.4(XRCC5):c.1550A>G (p.Asn517Ser)not specified [RCV004075028]uncertain significance2216148156216148156Humanname
156298879CV2248563single nucleotide variantNM_021141.4(XRCC5):c.1415C>G (p.Thr472Ser)not specified [RCV004121759]uncertain significance2216141258216141258Humanname
156306825CV2252778single nucleotide variantNM_021141.4(XRCC5):c.1889C>T (p.Pro630Leu)not specified [RCV004118618]likely benign2216190279216190279Humanname
155900998CV2298128single nucleotide variantNM_021141.4(XRCC5):c.1427T>G (p.Leu476Trp)not specified [RCV004159793]uncertain significance2216141270216141270Humanname
156204326CV2300802single nucleotide variantNM_021141.4(XRCC5):c.1355A>G (p.Asn452Ser)not specified [RCV004157733]likely benign2216141198216141198Humanname
156283650CV2317477single nucleotide variantNM_021141.4(XRCC5):c.1732G>C (p.Val578Leu)not specified [RCV004172442]uncertain significance2216160129216160129Humanname
156338886CV2370805single nucleotide variantNM_021141.4(XRCC5):c.1124T>G (p.Val375Gly)not specified [RCV004209199]uncertain significance2216137098216137098Humanname
329382372CV2424447single nucleotide variantNM_021141.4(XRCC5):c.1928G>A (p.Arg643Gln)not specified [RCV004252339]uncertain significance2216190318216190318Humanname
329383643CV2425053single nucleotide variantNM_021141.4(XRCC5):c.1861G>A (p.Glu621Lys)not specified [RCV004250709]uncertain significance2216190251216190251Humanname
329402182CV2454039single nucleotide variantNM_021141.4(XRCC5):c.1769G>A (p.Gly590Glu)not specified [RCV004271690]uncertain significance2216161983216161983Humanname
401745246CV2681226single nucleotide variantNM_021141.4(XRCC5):c.1219G>A (p.Val407Met)not specified [RCV004289364]uncertain significance2216137193216137193Humanname
401733787CV2687833single nucleotide variantNM_021141.4(XRCC5):c.1961G>A (p.Arg654His)not specified [RCV004303142]uncertain significance2216192655216192655Humanname
401855784CV2757437single nucleotide variantNM_021141.4(XRCC5):c.1796G>A (p.Arg599His)not specified [RCV004340831]uncertain significance2216162010216162010Humanname
401870377CV2765915single nucleotide variantNM_021141.4(XRCC5):c.1958A>G (p.Gln653Arg)not specified [RCV004337943]uncertain significance2216192652216192652Humanname
401878756CV2770159single nucleotide variantNM_021141.4(XRCC5):c.2132C>A (p.Pro711Gln)not specified [RCV004356057]uncertain significance2216204344216204344Humanname
401878459CV2774398single nucleotide variantNM_021141.4(XRCC5):c.1519C>G (p.Pro507Ala)not specified [RCV004347738]uncertain significance2216148125216148125Humanname
401877175CV2790076single nucleotide variantNM_021141.4(XRCC5):c.1400A>G (p.Asp467Gly)not specified [RCV004364026]uncertain significance2216141243216141243Humanname
407456137CV3493689single nucleotide variantNM_021141.4(XRCC5):c.1939A>G (p.Ile647Val)not specified [RCV004685839]uncertain significance2216190329216190329Humanname
407456140CV3493690single nucleotide variantNM_021141.4(XRCC5):c.1279A>C (p.Met427Leu)not specified [RCV004685840]uncertain significance2216138116216138116Humanname
597804773CV3630511single nucleotide variantNM_021141.4(XRCC5):c.1328A>G (p.Lys443Arg)not specified [RCV004882426]uncertain significance2216138165216138165Humanname
597804775CV3630512single nucleotide variantNM_021141.4(XRCC5):c.1159T>G (p.Leu387Val)not specified [RCV004882427]uncertain significance2216137133216137133Humanname
597804778CV3630514single nucleotide variantNM_021141.4(XRCC5):c.1066T>C (p.Phe356Leu)not specified [RCV004882429]uncertain significance2216132340216132340Humanname
597751750CV3630515single nucleotide variantNM_021141.4(XRCC5):c.2056A>G (p.Ile686Val)not specified [RCV004892814]uncertain significance2216194933216194933Humanname
597751756CV3630516single nucleotide variantNM_021141.4(XRCC5):c.1714G>A (p.Gly572Arg)not specified [RCV004892815]uncertain significance2216160111216160111Humanname
597751760CV3630517single nucleotide variantNM_021141.4(XRCC5):c.1823G>A (p.Ser608Asn)not specified [RCV004892816]uncertain significance2216162037216162037Humanname
598241715CV3933802single nucleotide variantNM_021141.4(XRCC5):c.1300A>G (p.Met434Val)not specified [RCV005296979]uncertain significance2216138137216138137Humanname
15100323CV697309single nucleotide variantNM_021141.4(XRCC5):c.1648G>T (p.Ala550Ser)not provided [RCV000958898]likely benign2216148254216148254Humanname