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Variants search result for Homo sapiens
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48 records found for search term Rhbg
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329379111CV2443300single nucleotide variantNM_020407.5(RHBG):c.7G>C (p.Gly3Arg)not specified [RCV004260101]uncertain significance1156369256156369256Humanname
156251491CV2394311single nucleotide variantNM_020407.5(RHBG):c.58C>T (p.Leu20Phe)not specified [RCV004238534]uncertain significance1156369307156369307Humanname
597788358CV3586536single nucleotide variantNM_020407.5(RHBG):c.82G>A (p.Val28Ile)not specified [RCV004855476]likely benign1156369331156369331Humanname
155985748CV2233918single nucleotide variantNM_020407.5(RHBG):c.229T>G (p.Phe77Val)not specified [RCV004104271]uncertain significance1156377342156377342Humanname
155981233CV2244053single nucleotide variantNM_020407.5(RHBG):c.256G>A (p.Gly86Ser)not specified [RCV004599471]uncertain significance1156377369156377369Humanname
156085385CV2244613single nucleotide variantNM_020407.5(RHBG):c.103C>T (p.Arg35Cys)not specified [RCV004102334]uncertain significance1156369352156369352Humanname
156162061CV2319521single nucleotide variantNM_020407.5(RHBG):c.130C>G (p.Leu44Val)not specified [RCV004185090]uncertain significance1156369379156369379Humanname
156036596CV2373998single nucleotide variantNM_020407.5(RHBG):c.197A>G (p.Asp66Gly)not specified [RCV004227128]uncertain significance1156377310156377310Humanname
407474570CV3472912single nucleotide variantNM_020407.5(RHBG):c.235A>G (p.Met79Val)not specified [RCV004663034]uncertain significance1156377348156377348Humanname
598189944CV3902686single nucleotide variantNM_020407.5(RHBG):c.182A>T (p.Tyr61Phe)not specified [RCV005266781]uncertain significance1156369431156369431Humanname
155918483CV2205892single nucleotide variantNM_020407.5(RHBG):c.860C>T (p.Ala287Val)not specified [RCV004078328]uncertain significance1156381825156381825Humanname
155925425CV2211829single nucleotide variantNM_020407.5(RHBG):c.977C>T (p.Thr326Met)not specified [RCV004086655]uncertain significance1156381942156381942Humanname
156279998CV2224057single nucleotide variantNM_020407.5(RHBG):c.472C>A (p.Leu158Met)not specified [RCV004095931]uncertain significance1156378087156378087Humanname
156293863CV2233584single nucleotide variantNM_020407.5(RHBG):c.563T>G (p.Phe188Cys)not specified [RCV004100057]uncertain significance1156378289156378289Humanname
156044039CV2397070single nucleotide variantNM_020407.5(RHBG):c.748A>T (p.Thr250Ser)not specified [RCV004236581]uncertain significance1156381421156381421Humanname
156094641CV2398854single nucleotide variantNM_020407.5(RHBG):c.752C>T (p.Ala251Val)not specified [RCV004245176]uncertain significance1156381425156381425Humanname
329397018CV2459833single nucleotide variantNM_020407.5(RHBG):c.403G>A (p.Ala135Thr)not specified [RCV004279333]uncertain significance1156378018156378018Humanname
401736884CV2699620single nucleotide variantNM_020407.5(RHBG):c.589T>C (p.Ser197Pro)not specified [RCV004299807]uncertain significance1156378315156378315Humanname
401768374CV2716401single nucleotide variantNM_020407.5(RHBG):c.934T>A (p.Phe312Ile)not specified [RCV004325714]uncertain significance1156381899156381899Humanname
405716832CV3309376single nucleotide variantNM_020407.5(RHBG):c.409C>G (p.Leu137Val)not specified [RCV004449315]uncertain significance1156378024156378024Humanname
405716843CV3309377single nucleotide variantNM_020407.5(RHBG):c.550A>T (p.Thr184Ser)not specified [RCV004449316]uncertain significance1156378276156378276Humanname
405716849CV3309378single nucleotide variantNM_020407.5(RHBG):c.903G>A (p.Met301Ile)not specified [RCV004449317]uncertain significance1156381868156381868Humanname
407474558CV3472909single nucleotide variantNM_020407.5(RHBG):c.610C>G (p.Gln204Glu)not specified [RCV004663031]uncertain significance1156378336156378336Humanname
597776151CV3586529single nucleotide variantNM_020407.5(RHBG):c.406G>A (p.Val136Met)not specified [RCV004852438]uncertain significance1156378021156378021Humanname
597776155CV3586530single nucleotide variantNM_020407.5(RHBG):c.745C>T (p.Arg249Trp)not specified [RCV004852439]uncertain significance1156381418156381418Humanname
597776159CV3586531single nucleotide variantNM_020407.5(RHBG):c.618G>C (p.Glu206Asp)not specified [RCV004852440]uncertain significance1156378344156378344Humanname
597776162CV3586533single nucleotide variantNM_020407.5(RHBG):c.401G>C (p.Gly134Ala)not specified [RCV004852441]uncertain significance1156378016156378016Humanname
597788351CV3586534single nucleotide variantNM_020407.5(RHBG):c.940G>C (p.Ala314Pro)not specified [RCV004855474]uncertain significance1156381905156381905Humanname
598189952CV3902687single nucleotide variantNM_020407.5(RHBG):c.575T>A (p.Phe192Tyr)not specified [RCV005266782]uncertain significance1156378301156378301Humanname
8628977CV84120single nucleotide variantNM_020407.5(RHBG):c.590C>T (p.Ser197Leu)not specified [RCV005266779]uncertain significance|not provided1156378316156378316Humanname
156002848CV2288154single nucleotide variantNM_020407.5(RHBG):c.1186G>A (p.Gly396Arg)not specified [RCV004149677]uncertain significance1156382821156382821Humanname
155970669CV2309206single nucleotide variantNM_020407.5(RHBG):c.1232G>A (p.Gly411Glu)not specified [RCV004171550]uncertain significance1156382867156382867Humanname
156113728CV2349147single nucleotide variantNM_020407.5(RHBG):c.1225G>A (p.Gly409Ser)not specified [RCV004205985]likely benign1156382860156382860Humanname
156259113CV2366213single nucleotide variantNM_020407.5(RHBG):c.1222G>C (p.Gly408Arg)not specified [RCV004210232]uncertain significance1156382857156382857Humanname
156087828CV2388230single nucleotide variantNM_020407.5(RHBG):c.1141G>C (p.Glu381Gln)not specified [RCV004234688]uncertain significance1156382776156382776Humanname
329367557CV2427441single nucleotide variantNM_020407.5(RHBG):c.1073T>C (p.Leu358Pro)not specified [RCV004248292]uncertain significance1156382162156382162Humanname
329356500CV2430780single nucleotide variantNM_020407.5(RHBG):c.1108G>A (p.Asp370Asn)not specified [RCV004253957]uncertain significance1156382197156382197Humanname
401754436CV2685268single nucleotide variantNM_020407.5(RHBG):c.1271C>A (p.Pro424Gln)not specified [RCV004289812]uncertain significance1156384563156384563Humanname
401888972CV2761618single nucleotide variantNM_020407.5(RHBG):c.1271C>G (p.Pro424Arg)not specified [RCV004337243]uncertain significance1156384563156384563Humanname
401885318CV2768078single nucleotide variantNM_020407.5(RHBG):c.1054G>A (p.Gly352Arg)not specified [RCV004348312]uncertain significance1156382143156382143Humanname
405716813CV3309373single nucleotide variantNM_020407.5(RHBG):c.1136T>C (p.Ile379Thr)not specified [RCV004449312]uncertain significance1156382771156382771Humanname
405716820CV3309374single nucleotide variantNM_020407.5(RHBG):c.1148A>G (p.Gln383Arg)not specified [RCV004449313]uncertain significance1156382783156382783Humanname
405716826CV3309375single nucleotide variantNM_020407.5(RHBG):c.1246A>G (p.Lys416Glu)not specified [RCV004449314]uncertain significance1156384538156384538Humanname
407474567CV3472911single nucleotide variantNM_020407.5(RHBG):c.1270C>G (p.Pro424Ala)not specified [RCV004663033]uncertain significance1156384562156384562Humanname
407474576CV3472913single nucleotide variantNM_020407.5(RHBG):c.1111G>A (p.Gly371Ser)not specified [RCV004663035]uncertain significance1156382200156382200Humanname
597788345CV3586532single nucleotide variantNM_020407.5(RHBG):c.1046G>C (p.Gly349Ala)not specified [RCV004855473]uncertain significance1156382135156382135Humanname
597788354CV3586535single nucleotide variantNM_020407.5(RHBG):c.1049T>G (p.Val350Gly)not specified [RCV004855475]uncertain significance1156382138156382138Humanname
598189936CV3902685single nucleotide variantNM_020407.5(RHBG):c.1225G>T (p.Gly409Cys)not specified [RCV005266780]uncertain significance1156382860156382860Humanname