Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.42962995T>ACA356792296GRXCR1c.488T>A (p.Phe163Tyr)
c.125T>A (p.Phe42Tyr)
4g.42962995T>CCA356792297GRXCR1c.488T>C (p.Phe163Ser)
c.125T>C (p.Phe42Ser)
 dbSNP COSMIC
4g.42962995T>GCA356792298GRXCR1c.488T>G (p.Phe163Cys)
c.125T>G (p.Phe42Cys)
4g.42962995T=CA1453073777GRXCR1c.488T= (p.Phe163=)
c.125T= (p.Phe42=)
4g.42962996C>ACA356792299GRXCR1c.489C>A (p.Phe163Leu)
c.126C>A (p.Phe42Leu)
4g.42962996C>GCA356792300GRXCR1c.489C>G (p.Phe163Leu)
c.126C>G (p.Phe42Leu)
4g.42962996C>TCA439191591GRXCR1c.489C>T (p.Phe163=)
c.126C>T (p.Phe42=)
4g.42962997C>ACA356792301GRXCR1c.490C>A (p.Gln164Lys)
c.127C>A (p.Gln43Lys)
4g.42962997C>GCA356792302GRXCR1c.490C>G (p.Gln164Glu)
c.127C>G (p.Gln43Glu)
4g.42962997C>TCA356792303GRXCR1c.490C>T (p.Gln164Ter)
c.127C>T (p.Gln43Ter)
4g.42962998A>CCA356792305GRXCR1c.491A>C (p.Gln164Pro)
c.128A>C (p.Gln43Pro)
4g.42962998A>GCA356792306GRXCR1c.491A>G (p.Gln164Arg)
c.128A>G (p.Gln43Arg)
4g.42962998A>TCA356792304GRXCR1c.491A>T (p.Gln164Leu)
c.128A>T (p.Gln43Leu)
4g.42962999A>CCA356792307GRXCR1c.492A>C (p.Gln164His)
c.129A>C (p.Gln43His)
4g.42962999A>GCA439191593GRXCR1c.492A>G (p.Gln164=)
c.129A>G (p.Gln43=)
4g.42962999A>TCA356792308GRXCR1c.492A>T (p.Gln164His)
c.129A>T (p.Gln43His)
4g.42963000A>CCA356792309GRXCR1c.493A>C (p.Asn165His)
c.130A>C (p.Asn44His)
4g.42963000A>GCA356792310GRXCR1c.493A>G (p.Asn165Asp)
c.130A>G (p.Asn44Asp)
4g.42963000A>TCA356792311GRXCR1c.493A>T (p.Asn165Tyr)
c.130A>T (p.Asn44Tyr)
4g.42963001A=CA1453073778GRXCR1c.494A= (p.Asn165=)
c.131A= (p.Asn44=)
4g.42963001A>CCA356792312GRXCR1c.494A>C (p.Asn165Thr)
c.131A>C (p.Asn44Thr)
4g.42963001A>GCA2904421GRXCR1c.494A>G (p.Asn165Ser)
c.131A>G (p.Asn44Ser)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.42963001A>TCA356792313GRXCR1c.494A>T (p.Asn165Ile)
c.131A>T (p.Asn44Ile)
4g.42963002C>ACA356792314GRXCR1c.495C>A (p.Asn165Lys)
c.132C>A (p.Asn44Lys)
4g.42963002C=CA1453073779GRXCR1c.495C= (p.Asn165=)
c.132C= (p.Asn44=)
4g.42963002C>GCA356792315GRXCR1c.495C>G (p.Asn165Lys)
c.132C>G (p.Asn44Lys)
4g.42963002C>TCA439191594GRXCR1c.495C>T (p.Asn165=)
c.132C>T (p.Asn44=)
 dbSNP gnomAD v4
4g.42963003C>ACA356792316GRXCR1c.496C>A (p.His166Asn)
c.133C>A (p.His45Asn)
4g.42963003C=CA1453073780GRXCR1c.496C= (p.His166=)
c.133C= (p.His45=)
4g.42963003C>GCA356792317GRXCR1c.496C>G (p.His166Asp)
c.133C>G (p.His45Asp)
4g.42963003C>TCA356792318GRXCR1c.496C>T (p.His166Tyr)
c.133C>T (p.His45Tyr)
 dbSNP gnomAD v4
4g.42963004A=CA1453073781GRXCR1c.497A= (p.His166=)
c.134A= (p.His45=)
4g.42963004A>CCA356792320GRXCR1c.497A>C (p.His166Pro)
c.134A>C (p.His45Pro)
4g.42963004A>GCA2904422GRXCR1c.497A>G (p.His166Arg)
c.134A>G (p.His45Arg)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.42963004A>TCA356792319GRXCR1c.497A>T (p.His166Leu)
c.134A>T (p.His45Leu)
4g.42963005T>ACA356792321GRXCR1c.498T>A (p.His166Gln)
c.135T>A (p.His45Gln)
4g.42963005T>CCA439191596GRXCR1c.498T>C (p.His166=)
c.135T>C (p.His45=)
 dbSNP
4g.42963005T>GCA356792322GRXCR1c.498T>G (p.His166Gln)
c.135T>G (p.His45Gln)
4g.42963005T=CA1453073782GRXCR1c.498T= (p.His166=)
c.135T= (p.His45=)
4g.42963006C>ACA356792323GRXCR1c.499C>A (p.Arg167Ser)
c.136C>A (p.Arg46Ser)
 COSMIC
4g.42963006C=CA1453073783GRXCR1c.499C= (p.Arg167=)
c.136C= (p.Arg46=)
4g.42963006C>GCA356792324GRXCR1c.499C>G (p.Arg167Gly)
c.136C>G (p.Arg46Gly)
 dbSNP gnomAD v4
4g.42963006C>TCA2904423GRXCR1c.499C>T (p.Arg167Cys)
c.136C>T (p.Arg46Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.42963007G>ACA2904424GRXCR1c.500G>A (p.Arg167His)
c.137G>A (p.Arg46His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.42963007G>CCA356792325GRXCR1c.500G>C (p.Arg167Pro)
c.137G>C (p.Arg46Pro)
4g.42963007G=CA1453073784GRXCR1c.500G= (p.Arg167=)
c.137G= (p.Arg46=)
4g.42963007G>TCA356792326GRXCR1c.500G>T (p.Arg167Leu)
c.137G>T (p.Arg46Leu)
4g.42963008C>ACA439191599GRXCR1c.501C>A (p.Arg167=)
c.138C>A (p.Arg46=)
 dbSNP gnomAD v4
4g.42963008C=CA1453073785GRXCR1c.501C= (p.Arg167=)
c.138C= (p.Arg46=)
4g.42963008C>GCA439191601GRXCR1c.501C>G (p.Arg167=)
c.138C>G (p.Arg46=)
4g.42963008C>TCA439191600GRXCR1c.501C>T (p.Arg167=)
c.138C>T (p.Arg46=)
 dbSNP gnomAD v4
4g.42963009G>ACA2904425GRXCR1c.502G>A (p.Val168Ile)
c.139G>A (p.Val47Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.42963009G>CCA356792327GRXCR1c.502G>C (p.Val168Leu)
c.139G>C (p.Val47Leu)
4g.42963009G=CA1453073786GRXCR1c.502G= (p.Val168=)
c.139G= (p.Val47=)
4g.42963009G>TCA356792328GRXCR1c.502G>T (p.Val168Leu)
c.139G>T (p.Val47Leu)
 gnomAD v4
4g.42963010T>ACA356792329GRXCR1c.503T>A (p.Val168Glu)
c.140T>A (p.Val47Glu)
4g.42963010T>CCA356792330GRXCR1c.503T>C (p.Val168Ala)
c.140T>C (p.Val47Ala)
4g.42963010T>GCA356792331GRXCR1c.503T>G (p.Val168Gly)
c.140T>G (p.Val47Gly)
4g.42963011A>CCA439191605GRXCR1c.504A>C (p.Val168=)
c.141A>C (p.Val47=)
4g.42963011A>GCA439191604GRXCR1c.504A>G (p.Val168=)
c.141A>G (p.Val47=)
4g.42963011A>TCA439191603GRXCR1c.504A>T (p.Val168=)
c.141A>T (p.Val47=)
4g.42963012A>CCA356792333GRXCR1c.505A>C (p.Lys169Gln)
c.142A>C (p.Lys48Gln)
 COSMIC
4g.42963012A>GCA356792334GRXCR1c.505A>G (p.Lys169Glu)
c.142A>G (p.Lys48Glu)
4g.42963012A>TCA356792332GRXCR1c.505A>T (p.Lys169Ter)
c.142A>T (p.Lys48Ter)
4g.42963013A=CA1453073787GRXCR1c.506A= (p.Lys169=)
c.143A= (p.Lys48=)
4g.42963013A>CCA356792335GRXCR1c.506A>C (p.Lys169Thr)
c.143A>C (p.Lys48Thr)
 COSMIC
4g.42963013A>GCA356792336GRXCR1c.506A>G (p.Lys169Arg)
c.143A>G (p.Lys48Arg)
4g.42963013A>TCA2904426GRXCR1c.506A>T (p.Lys169Ile)
c.143A>T (p.Lys48Ile)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.42963014A>CCA356792337GRXCR1c.507A>C (p.Lys169Asn)
c.144A>C (p.Lys48Asn)
4g.42963014A>GCA439191608GRXCR1c.507A>G (p.Lys169=)
c.144A>G (p.Lys48=)
4g.42963014A>TCA356792338GRXCR1c.507A>T (p.Lys169Asn)
c.144A>T (p.Lys48Asn)
 ClinVar
4g.42963015T>ACA356792339GRXCR1c.508T>A (p.Phe170Ile)
c.145T>A (p.Phe49Ile)
 gnomAD v4
4g.42963015T>CCA356792340GRXCR1c.508T>C (p.Phe170Leu)
c.145T>C (p.Phe49Leu)
4g.42963015T>GCA356792341GRXCR1c.508T>G (p.Phe170Val)
c.145T>G (p.Phe49Val)
4g.42963016T>ACA356792342GRXCR1c.509T>A (p.Phe170Tyr)
c.146T>A (p.Phe49Tyr)
4g.42963016T>CCA356792343GRXCR1c.509T>C (p.Phe170Ser)
c.146T>C (p.Phe49Ser)
 dbSNP
4g.42963016T>GCA356792344GRXCR1c.509T>G (p.Phe170Cys)
c.146T>G (p.Phe49Cys)
 COSMIC
4g.42963016T=CA1453073788GRXCR1c.509T= (p.Phe170=)
c.146T= (p.Phe49=)
4g.42963017T>ACA356792345GRXCR1c.510T>A (p.Phe170Leu)
c.147T>A (p.Phe49Leu)
4g.42963017T>CCA439191612GRXCR1c.510T>C (p.Phe170=)
c.147T>C (p.Phe49=)
 gnomAD v4
4g.42963017T>GCA356792346GRXCR1c.510T>G (p.Phe170Leu)
c.147T>G (p.Phe49Leu)
4g.42963018G>ACA356792347GRXCR1c.511G>A (p.Glu171Lys)
c.148G>A (p.Glu50Lys)
4g.42963018G>CCA356792348GRXCR1c.511G>C (p.Glu171Gln)
c.148G>C (p.Glu50Gln)
4g.42963018G>TCA356792349GRXCR1c.511G>T (p.Glu171Ter)
c.148G>T (p.Glu50Ter)
4g.42963019A>CCA356792352GRXCR1c.512A>C (p.Glu171Ala)
c.149A>C (p.Glu50Ala)
4g.42963019A>GCA356792350GRXCR1c.512A>G (p.Glu171Gly)
c.149A>G (p.Glu50Gly)
4g.42963019A>TCA356792351GRXCR1c.512A>T (p.Glu171Val)
c.149A>T (p.Glu50Val)
4g.42963020A=CA1453073789GRXCR1c.513A= (p.Glu171=)
c.150A= (p.Glu50=)
4g.42963020A>CCA356792353GRXCR1c.513A>C (p.Glu171Asp)
c.150A>C (p.Glu50Asp)
4g.42963020A>GCA439191616GRXCR1c.513A>G (p.Glu171=)
c.150A>G (p.Glu50=)
 dbSNP gnomAD v3 gnomAD v4
4g.42963020A>TCA356792354GRXCR1c.513A>T (p.Glu171Asp)
c.150A>T (p.Glu50Asp)
4g.42963021G>ACA356792355GRXCR1c.514G>A (p.Glu172Lys)
c.151G>A (p.Glu51Lys)
 gnomAD v4
4g.42963021G>CCA356792356GRXCR1c.514G>C (p.Glu172Gln)
c.151G>C (p.Glu51Gln)
4g.42963021G>TCA356792357GRXCR1c.514G>T (p.Glu172Ter)
c.151G>T (p.Glu51Ter)
4g.42963022A=CA1453073790GRXCR1c.515A= (p.Glu172=)
c.152A= (p.Glu51=)
4g.42963022A>CCA356792358GRXCR1c.515A>C (p.Glu172Ala)
c.152A>C (p.Glu51Ala)
4g.42963022A>GCA356792359GRXCR1c.515A>G (p.Glu172Gly)
c.152A>G (p.Glu51Gly)
 dbSNP gnomAD v2 gnomAD v4
4g.42963022A>TCA356792360GRXCR1c.515A>T (p.Glu172Val)
c.152A>T (p.Glu51Val)
4g.42963023G>ACA439191620GRXCR1c.516G>A (p.Glu172=)
c.153G>A (p.Glu51=)
 dbSNP gnomAD v4
4g.42963023G>CCA356792361GRXCR1c.516G>C (p.Glu172Asp)
c.153G>C (p.Glu51Asp)
4g.42963023G=CA1453073791GRXCR1c.516G= (p.Glu172=)
c.153G= (p.Glu51=)
4g.42963023G>TCA356792362GRXCR1c.516G>T (p.Glu172Asp)
c.153G>T (p.Glu51Asp)
4g.42963024A>CCA356792364GRXCR1c.517A>C (p.Lys173Gln)
c.154A>C (p.Lys52Gln)
4g.42963024A>GCA356792365GRXCR1c.517A>G (p.Lys173Glu)
c.154A>G (p.Lys52Glu)
4g.42963024A>TCA356792363GRXCR1c.517A>T (p.Lys173Ter)
c.154A>T (p.Lys52Ter)
4g.42963028delCA2670496482GRXCR1c.521del (p.Asn174ThrfsTer2)
c.158del (p.Asn53ThrfsTer2)
 gnomAD v4
4g.42963025A>CCA356792366GRXCR1c.518A>C (p.Lys173Thr)
c.155A>C (p.Lys52Thr)
4g.42963025A>GCA356792367GRXCR1c.518A>G (p.Lys173Arg)
c.155A>G (p.Lys52Arg)
4g.42963025A>TCA356792368GRXCR1c.518A>T (p.Lys173Ile)
c.155A>T (p.Lys52Ile)
 COSMIC
4g.42963026A>CCA356792369GRXCR1c.519A>C (p.Lys173Asn)
c.156A>C (p.Lys52Asn)
4g.42963026A>GCA439191624GRXCR1c.519A>G (p.Lys173=)
c.156A>G (p.Lys52=)
4g.42963026A>TCA356792370GRXCR1c.519A>T (p.Lys173Asn)
c.156A>T (p.Lys52Asn)
4g.42963027A>CCA356792373GRXCR1c.520A>C (p.Asn174His)
c.157A>C (p.Asn53His)
4g.42963027A>GCA356792371GRXCR1c.520A>G (p.Asn174Asp)
c.157A>G (p.Asn53Asp)
4g.42963027A>TCA356792372GRXCR1c.520A>T (p.Asn174Tyr)
c.157A>T (p.Asn53Tyr)
4g.42963028A>CCA356792374GRXCR1c.521A>C (p.Asn174Thr)
c.158A>C (p.Asn53Thr)
4g.42963028A>GCA356792375GRXCR1c.521A>G (p.Asn174Ser)
c.158A>G (p.Asn53Ser)
 gnomAD v4
4g.42963028A>TCA356792376GRXCR1c.521A>T (p.Asn174Ile)
c.158A>T (p.Asn53Ile)
4g.42963029C>ACA356792377GRXCR1c.522C>A (p.Asn174Lys)
c.159C>A (p.Asn53Lys)
4g.42963029C>GCA356792378GRXCR1c.522C>G (p.Asn174Lys)
c.159C>G (p.Asn53Lys)
4g.42963029C>TCA439191626GRXCR1c.522C>T (p.Asn174=)
c.159C>T (p.Asn53=)
 COSMIC
4g.42963030A=CA1453073792GRXCR1c.523A= (p.Ile175=)
c.160A= (p.Ile54=)
4g.42963030A>CCA356792379GRXCR1c.523A>C (p.Ile175Leu)
c.160A>C (p.Ile54Leu)
4g.42963030A>GCA2904427GRXCR1c.523A>G (p.Ile175Val)
c.160A>G (p.Ile54Val)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.42963030A>TCA356792380GRXCR1c.523A>T (p.Ile175Leu)
c.160A>T (p.Ile54Leu)
 gnomAD v4
4g.42963031T>ACA356792381GRXCR1c.524T>A (p.Ile175Lys)
c.161T>A (p.Ile54Lys)
4g.42963031T>CCA2904428GRXCR1c.524T>C (p.Ile175Thr)
c.161T>C (p.Ile54Thr)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.42963031T>GCA356792382GRXCR1c.524T>G (p.Ile175Arg)
c.161T>G (p.Ile54Arg)
4g.42963031T=CA1453073793GRXCR1c.524T= (p.Ile175=)
c.161T= (p.Ile54=)
4g.42963031_42963036delinsTAGCCCCA1453073794GRXCR1c.524_529delinsTAGCCC (p.Ile175=)
c.161_166delinsTAGCCC (p.Ile54=)
4g.42963032A>CCA439191630GRXCR1c.525A>C (p.Ile175=)
c.162A>C (p.Ile54=)
4g.42963032A>GCA356792383GRXCR1c.525A>G (p.Ile175Met)
c.162A>G (p.Ile54Met)
4g.42963032A>TCA439191631GRXCR1c.525A>T (p.Ile175=)
c.162A>T (p.Ile54=)
4g.42963032_42963036delCA1453073795GRXCR1c.525_529del (p.Ala176GlufsTer3)
c.162_166del (p.Ala55GlufsTer3)
 dbSNP
4g.42963033G>ACA356792384GRXCR1c.526G>A (p.Ala176Thr)
c.163G>A (p.Ala55Thr)
 gnomAD v4
4g.42963033G>CCA356792385GRXCR1c.526G>C (p.Ala176Pro)
c.163G>C (p.Ala55Pro)
4g.42963033G=CA1453073796GRXCR1c.526G= (p.Ala176=)
c.163G= (p.Ala55=)
4g.42963033G>TCA356792386GRXCR1c.526G>T (p.Ala176Ser)
c.163G>T (p.Ala55Ser)
 dbSNP gnomAD v3 gnomAD v4
4g.42963034C>ACA356792387GRXCR1c.527C>A (p.Ala176Asp)
c.164C>A (p.Ala55Asp)
4g.42963034C=CA1453073797GRXCR1c.527C= (p.Ala176=)
c.164C= (p.Ala55=)
4g.42963034C>GCA356792388GRXCR1c.527C>G (p.Ala176Gly)
c.164C>G (p.Ala55Gly)
4g.42963034C>TCA2904429GRXCR1c.527C>T (p.Ala176Val)
c.164C>T (p.Ala55Val)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.42963035C>ACA439191633GRXCR1c.528C>A (p.Ala176=)
c.165C>A (p.Ala55=)
4g.42963035C=CA1453073798GRXCR1c.528C= (p.Ala176=)
c.165C= (p.Ala55=)
4g.42963035C>GCA439191635GRXCR1c.528C>G (p.Ala176=)
c.165C>G (p.Ala55=)
4g.42963035C>TCA439191634GRXCR1c.528C>T (p.Ala176=)
c.165C>T (p.Ala55=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.42963036C>ACA2904430GRXCR1c.529C>A (p.Leu177Met)
c.166C>A (p.Leu56Met)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.42963036C=CA1453073799GRXCR1c.529C= (p.Leu177=)
c.166C= (p.Leu56=)
4g.42963036C>GCA356792389GRXCR1c.529C>G (p.Leu177Val)
c.166C>G (p.Leu56Val)
4g.42963036C>TCA439191636GRXCR1c.529C>T (p.Leu177=)
c.166C>T (p.Leu56=)
4g.42963037T>ACA356792390GRXCR1c.530T>A (p.Leu177Gln)
c.167T>A (p.Leu56Gln)
 COSMIC
4g.42963037T>CCA356792391GRXCR1c.530T>C (p.Leu177Pro)
c.167T>C (p.Leu56Pro)
4g.42963037T>GCA96311684GRXCR1c.530T>G (p.Leu177Arg)
c.167T>G (p.Leu56Arg)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.42963037T=CA1453073800GRXCR1c.530T= (p.Leu177=)
c.167T= (p.Leu56=)
4g.42963038G>ACA439191638GRXCR1c.531G>A (p.Leu177=)
c.168G>A (p.Leu56=)
4g.42963038G>CCA439191639GRXCR1c.531G>C (p.Leu177=)
c.168G>C (p.Leu56=)
 dbSNP
4g.42963038G=CA1453073801GRXCR1c.531G= (p.Leu177=)
c.168G= (p.Leu56=)
4g.42963038G>TCA439191640GRXCR1c.531G>T (p.Leu177=)
c.168G>T (p.Leu56=)
4g.42963039A>CCA356792392GRXCR1c.532A>C (p.Asn178His)
c.169A>C (p.Asn57His)
4g.42963039A>GCA356792393GRXCR1c.532A>G (p.Asn178Asp)
c.169A>G (p.Asn57Asp)
4g.42963039A>TCA356792394GRXCR1c.532A>T (p.Asn178Tyr)
c.169A>T (p.Asn57Tyr)
4g.42963040A=CA1453073802GRXCR1c.533A= (p.Asn178=)
c.170A= (p.Asn57=)
4g.42963040A>CCA356792395GRXCR1c.533A>C (p.Asn178Thr)
c.170A>C (p.Asn57Thr)
4g.42963040A>GCA356792396GRXCR1c.533A>G (p.Asn178Ser)
c.170A>G (p.Asn57Ser)
 dbSNP gnomAD v4
4g.42963040A>TCA356792397GRXCR1c.533A>T (p.Asn178Ile)
c.170A>T (p.Asn57Ile)
4g.42963041T>ACA356792399GRXCR1c.534T>A (p.Asn178Lys)
c.171T>A (p.Asn57Lys)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.42963041T>CCA439191644GRXCR1c.534T>C (p.Asn178=)
c.171T>C (p.Asn57=)
4g.42963041T>GCA356792398GRXCR1c.534T>G (p.Asn178Lys)
c.171T>G (p.Asn57Lys)
 gnomAD v4
4g.42963041T=CA1453073803GRXCR1c.534T= (p.Asn178=)
c.171T= (p.Asn57=)
4g.42963042G>ACA356792400GRXCR1c.535G>A (p.Gly179Ser)
c.172G>A (p.Gly58Ser)
 dbSNP gnomAD v2 gnomAD v4
4g.42963042G>CCA356792401GRXCR1c.535G>C (p.Gly179Arg)
c.172G>C (p.Gly58Arg)
4g.42963042G=CA1453073804GRXCR1c.535G= (p.Gly179=)
c.172G= (p.Gly58=)
4g.42963042G>TCA356792402GRXCR1c.535G>T (p.Gly179Cys)
c.172G>T (p.Gly58Cys)
 dbSNP
4g.42963043G>ACA356792403GRXCR1c.536G>A (p.Gly179Asp)
c.173G>A (p.Gly58Asp)
 dbSNP gnomAD v2 gnomAD v4
4g.42963043G>CCA356792404GRXCR1c.536G>C (p.Gly179Ala)
c.173G>C (p.Gly58Ala)
4g.42963043G=CA1453073805GRXCR1c.536G= (p.Gly179=)
c.173G= (p.Gly58=)
4g.42963043G>TCA356792405GRXCR1c.536G>T (p.Gly179Val)
c.173G>T (p.Gly58Val)
4g.42963044T>ACA439191648GRXCR1c.537T>A (p.Gly179=)
c.174T>A (p.Gly58=)
4g.42963044T>CCA439191646GRXCR1c.537T>C (p.Gly179=)
c.174T>C (p.Gly58=)
 gnomAD v4
4g.42963044T>GCA439191647GRXCR1c.537T>G (p.Gly179=)
c.174T>G (p.Gly58=)
4g.42963044_42963045insAACA2557343122GRXCR1c.537_538insAA (p.Glu180LysfsTer7)
c.174_175insAA (p.Glu59LysfsTer7)
4g.42963045G>ACA356792408GRXCR1c.538G>A (p.Glu180Lys)
c.175G>A (p.Glu59Lys)
 gnomAD v4
4g.42963045G>CCA356792406GRXCR1c.538G>C (p.Glu180Gln)
c.175G>C (p.Glu59Gln)
4g.42963045G>TCA356792407GRXCR1c.538G>T (p.Glu180Ter)
c.175G>T (p.Glu59Ter)
 COSMIC
4g.42963046A>CCA356792409GRXCR1c.539A>C (p.Glu180Ala)
c.176A>C (p.Glu59Ala)
4g.42963046A>GCA356792410GRXCR1c.539A>G (p.Glu180Gly)
c.176A>G (p.Glu59Gly)
4g.42963046A>TCA356792411GRXCR1c.539A>T (p.Glu180Val)
c.176A>T (p.Glu59Val)
4g.42963047A>CCA356792412GRXCR1c.540A>C (p.Glu180Asp)
c.177A>C (p.Glu59Asp)
4g.42963047A>GCA439191651GRXCR1c.540A>G (p.Glu180=)
c.177A>G (p.Glu59=)
 gnomAD v4
4g.42963047A>TCA356792413GRXCR1c.540A>T (p.Glu180Asp)
c.177A>T (p.Glu59Asp)
4g.42963049_42963050delCA2514245875GRXCR1c.542_543del (p.Tyr181TrpfsTer13)
c.179_180del (p.Tyr60TrpfsTer13)
4g.42963048T>ACA356792414GRXCR1c.541T>A (p.Tyr181Asn)
c.178T>A (p.Tyr60Asn)
4g.42963048T>CCA356792415GRXCR1c.541T>C (p.Tyr181His)
c.178T>C (p.Tyr60His)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.42963048T>GCA356792416GRXCR1c.541T>G (p.Tyr181Asp)
c.178T>G (p.Tyr60Asp)
4g.42963048T=CA1453073806GRXCR1c.541T= (p.Tyr181=)
c.178T= (p.Tyr60=)
4g.42963049A>CCA356792417GRXCR1c.542A>C (p.Tyr181Ser)
c.179A>C (p.Tyr60Ser)
4g.42963049A>GCA356792418GRXCR1c.542A>G (p.Tyr181Cys)
c.179A>G (p.Tyr60Cys)
4g.42963049A>TCA356792419GRXCR1c.542A>T (p.Tyr181Phe)
c.179A>T (p.Tyr60Phe)
4g.42963050T>ACA356792420GRXCR1c.543T>A (p.Tyr181Ter)
c.180T>A (p.Tyr60Ter)
4g.42963050T>CCA439191653GRXCR1c.543T>C (p.Tyr181=)
c.180T>C (p.Tyr60=)
 gnomAD v4 COSMIC
4g.42963050T>GCA356792421GRXCR1c.543T>G (p.Tyr181Ter)
c.180T>G (p.Tyr60Ter)
4g.42963051G>ACA356792422GRXCR1c.544G>A (p.Gly182Arg)
c.181G>A (p.Gly61Arg)
4g.42963051G>CCA356792424GRXCR1c.544G>C (p.Gly182Arg)
c.181G>C (p.Gly61Arg)
4g.42963051G>TCA356792423GRXCR1c.544G>T (p.Gly182Ter)
c.181G>T (p.Gly61Ter)
4g.42963052G>ACA356792425GRXCR1c.545G>A (p.Gly182Glu)
c.182G>A (p.Gly61Glu)
 dbSNP gnomAD v4 COSMIC
4g.42963052G>CCA356792426GRXCR1c.545G>C (p.Gly182Ala)
c.182G>C (p.Gly61Ala)
4g.42963052G=CA1453073807GRXCR1c.545G= (p.Gly182=)
c.182G= (p.Gly61=)
4g.42963052G>TCA356792427GRXCR1c.545G>T (p.Gly182Val)
c.182G>T (p.Gly61Val)
4g.42963053A>CCA439191656GRXCR1c.546A>C (p.Gly182=)
c.183A>C (p.Gly61=)
4g.42963053A>GCA439191657GRXCR1c.546A>G (p.Gly182=)
c.183A>G (p.Gly61=)
4g.42963053A>TCA439191658GRXCR1c.546A>T (p.Gly182=)
c.183A>T (p.Gly61=)
4g.42963056delCA2578076948GRXCR1c.549del (p.Glu184SerfsTer2)
c.186del (p.Glu63SerfsTer2)
4g.42963054A>CCA356792428GRXCR1c.547A>C (p.Lys183Gln)
c.184A>C (p.Lys62Gln)
4g.42963054A>GCA356792429GRXCR1c.547A>G (p.Lys183Glu)
c.184A>G (p.Lys62Glu)
4g.42963054A>TCA356792430GRXCR1c.547A>T (p.Lys183Ter)
c.184A>T (p.Lys62Ter)
4g.42963055A=CA1453073808GRXCR1c.548A= (p.Lys183=)
c.185A= (p.Lys62=)
4g.42963055A>CCA2904431GRXCR1c.548A>C (p.Lys183Thr)
c.185A>C (p.Lys62Thr)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.42963055A>GCA356792431GRXCR1c.548A>G (p.Lys183Arg)
c.185A>G (p.Lys62Arg)
 gnomAD v4
4g.42963055A>TCA356792432GRXCR1c.548A>T (p.Lys183Ile)
c.185A>T (p.Lys62Ile)
4g.42963056A=CA1453073809GRXCR1c.549A= (p.Lys183=)
c.186A= (p.Lys62=)
4g.42963056A>CCA356792433GRXCR1c.549A>C (p.Lys183Asn)
c.186A>C (p.Lys62Asn)
4g.42963056A>GCA2904432GRXCR1c.549A>G (p.Lys183=)
c.186A>G (p.Lys62=)
 dbSNP ExAC gnomAD v4
4g.42963056A>TCA356792434GRXCR1c.549A>T (p.Lys183Asn)
c.186A>T (p.Lys62Asn)
4g.42963057G>ACA356792437GRXCR1c.550G>A (p.Glu184Lys)
c.187G>A (p.Glu63Lys)
4g.42963057G>CCA356792436GRXCR1c.550G>C (p.Glu184Gln)
c.187G>C (p.Glu63Gln)
4g.42963057G>TCA356792435GRXCR1c.550G>T (p.Glu184Ter)
c.187G>T (p.Glu63Ter)
 ClinVar dbSNP
4g.42963058A=CA1453073810GRXCR1c.551A= (p.Glu184=)
c.188A= (p.Glu63=)
4g.42963058A>CCA356792438GRXCR1c.551A>C (p.Glu184Ala)
c.188A>C (p.Glu63Ala)
4g.42963058A>GCA356792439GRXCR1c.551A>G (p.Glu184Gly)
c.188A>G (p.Glu63Gly)
4g.42963058A>TCA10621111GRXCR1c.551A>T (p.Glu184Val)
c.188A>T (p.Glu63Val)
 ClinVar dbSNP gnomAD v2 gnomAD v4
4g.42963060_42963063delCA2670496483GRXCR1c.553_556del (p.Leu185ThrfsTer?)
c.190_193del (p.Leu64ThrfsTer?)
 gnomAD v4
4g.42963059G>ACA439191662GRXCR1c.552G>A (p.Glu184=)
c.189G>A (p.Glu63=)
 gnomAD v4
4g.42963059G>CCA356792440GRXCR1c.552G>C (p.Glu184Asp)
c.189G>C (p.Glu63Asp)
4g.42963059G>TCA356792441GRXCR1c.552G>T (p.Glu184Asp)
c.189G>T (p.Glu63Asp)
4g.42963060T>ACA356792442GRXCR1c.553T>A (p.Leu185Ile)
c.190T>A (p.Leu64Ile)
4g.42963060T>CCA439191663GRXCR1c.553T>C (p.Leu185=)
c.190T>C (p.Leu64=)
4g.42963060T>GCA356792443GRXCR1c.553T>G (p.Leu185Val)
c.190T>G (p.Leu64Val)
4g.42963061T>ACA356792444GRXCR1c.554T>A (p.Leu185Ter)
c.191T>A (p.Leu64Ter)
4g.42963061T>CCA356792445GRXCR1c.554T>C (p.Leu185Ser)
c.191T>C (p.Leu64Ser)
4g.42963061T>GCA356792446GRXCR1c.554T>G (p.Leu185Ter)
c.191T>G (p.Leu64Ter)
4g.42963062A>CCA356792447GRXCR1c.555A>C (p.Leu185Phe)
c.192A>C (p.Leu64Phe)
4g.42963062A>GCA439191667GRXCR1c.555A>G (p.Leu185=)
c.192A>G (p.Leu64=)
4g.42963062A>TCA356792448GRXCR1c.555A>T (p.Leu185Phe)
c.192A>T (p.Leu64Phe)
4g.42963063G>ACA356792451GRXCR1c.556G>A (p.Asp186Asn)
c.193G>A (p.Asp65Asn)
4g.42963063G>CCA356792450GRXCR1c.556G>C (p.Asp186His)
c.193G>C (p.Asp65His)
4g.42963063G>TCA356792449GRXCR1c.556G>T (p.Asp186Tyr)
c.193G>T (p.Asp65Tyr)
4g.42963064A=CA1453073811GRXCR1c.557A= (p.Asp186=)
c.194A= (p.Asp65=)
4g.42963064A>CCA2904433GRXCR1c.557A>C (p.Asp186Ala)
c.194A>C (p.Asp65Ala)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.42963064A>GCA356792453GRXCR1c.557A>G (p.Asp186Gly)
c.194A>G (p.Asp65Gly)
4g.42963064A>TCA356792452GRXCR1c.557A>T (p.Asp186Val)
c.194A>T (p.Asp65Val)
4g.42963065C>ACA356792454GRXCR1c.558C>A (p.Asp186Glu)
c.195C>A (p.Asp65Glu)
 dbSNP gnomAD v3 gnomAD v4
4g.42963065C=CA1453073812GRXCR1c.558C= (p.Asp186=)
c.195C= (p.Asp65=)
4g.42963065C>GCA356792455GRXCR1c.558C>G (p.Asp186Glu)
c.195C>G (p.Asp65Glu)
4g.42963065C>TCA2904434GRXCR1c.558C>T (p.Asp186=)
c.195C>T (p.Asp65=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.42963066G>ACA2904435GRXCR1c.559G>A (p.Glu187Lys)
c.196G>A (p.Glu66Lys)
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
4g.42963066G>CCA356792457GRXCR1c.559G>C (p.Glu187Gln)
c.196G>C (p.Glu66Gln)
 dbSNP
4g.42963066G=CA1453073813GRXCR1c.559G= (p.Glu187=)
c.196G= (p.Glu66=)
4g.42963066G>TCA356792456GRXCR1c.559G>T (p.Glu187Ter)
c.196G>T (p.Glu66Ter)
4g.42963067A>CCA356792458GRXCR1c.560A>C (p.Glu187Ala)
c.197A>C (p.Glu66Ala)
4g.42963067A>GCA356792460GRXCR1c.560A>G (p.Glu187Gly)
c.197A>G (p.Glu66Gly)
4g.42963067A>TCA356792459GRXCR1c.560A>T (p.Glu187Val)
c.197A>T (p.Glu66Val)
4g.42963068A=CA1453073814GRXCR1c.561A= (p.Glu187=)
c.198A= (p.Glu66=)
4g.42963068A>CCA356792461GRXCR1c.561A>C (p.Glu187Asp)
c.198A>C (p.Glu66Asp)
4g.42963068A>GCA2904436GRXCR1c.561A>G (p.Glu187=)
c.198A>G (p.Glu66=)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.42963068A>TCA356792462GRXCR1c.561A>T (p.Glu187Asp)
c.198A>T (p.Glu66Asp)
4g.42963069C>ACA439191708GRXCR1c.562C>A (p.Arg188=)
c.199C>A (p.Arg67=)
 gnomAD v4
4g.42963069C=CA1453073815GRXCR1c.562C= (p.Arg188=)
c.199C= (p.Arg67=)
4g.42963069C>GCA356792463GRXCR1c.562C>G (p.Arg188Gly)
c.199C>G (p.Arg67Gly)
4g.42963069C>TCA2904437GRXCR1c.562C>T (p.Arg188Ter)
c.199C>T (p.Arg67Ter)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.42963070G>ACA356792464GRXCR1c.563G>A (p.Arg188Gln)
c.200G>A (p.Arg67Gln)
 gnomAD v4 COSMIC
4g.42963070G>CCA356792465GRXCR1c.563G>C (p.Arg188Pro)
c.200G>C (p.Arg67Pro)
4g.42963070G>TCA356792466GRXCR1c.563G>T (p.Arg188Leu)
c.200G>T (p.Arg67Leu)
4g.42963071A=CA1453073816GRXCR1c.564A= (p.Arg188=)
c.201A= (p.Arg67=)
4g.42963071A>CCA439191712GRXCR1c.564A>C (p.Arg188=)
c.201A>C (p.Arg67=)
4g.42963071A>GCA439191713GRXCR1c.564A>G (p.Arg188=)
c.201A>G (p.Arg67=)
4g.42963071A>TCA439191714GRXCR1c.564A>T (p.Arg188=)
c.201A>T (p.Arg67=)
 dbSNP gnomAD v3 gnomAD v4
4g.42963072T>ACA356792467GRXCR1c.565T>A (p.Cys189Ser)
c.202T>A (p.Cys68Ser)
4g.42963072T>CCA356792468GRXCR1c.565T>C (p.Cys189Arg)
c.202T>C (p.Cys68Arg)
 dbSNP gnomAD v2 gnomAD v4
4g.42963072T>GCA356792469GRXCR1c.565T>G (p.Cys189Gly)
c.202T>G (p.Cys68Gly)
4g.42963072T=CA1453073817GRXCR1c.565T= (p.Cys189=)
c.202T= (p.Cys68=)
4g.42963073G>ACA356792470GRXCR1c.566G>A (p.Cys189Tyr)
c.203G>A (p.Cys68Tyr)
4g.42963073G>CCA356792471GRXCR1c.566G>C (p.Cys189Ser)
c.203G>C (p.Cys68Ser)
4g.42963073G>TCA356792472GRXCR1c.566G>T (p.Cys189Phe)
c.203G>T (p.Cys68Phe)
4g.42963074C>ACA356792473GRXCR1c.567C>A (p.Cys189Ter)
c.204C>A (p.Cys68Ter)
4g.42963074C>GCA356792474GRXCR1c.567C>G (p.Cys189Trp)
c.204C>G (p.Cys68Trp)
 gnomAD v4
4g.42963074C>TCA439191716GRXCR1c.567C>T (p.Cys189=)
c.204C>T (p.Cys68=)
4g.42963075C>ACA2904438GRXCR1c.568C>A (p.Arg190=)
c.205C>A (p.Arg69=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.42963075C=CA1453073818GRXCR1c.568C= (p.Arg190=)
c.205C= (p.Arg69=)
4g.42963075C>GCA356792476GRXCR1c.568C>G (p.Arg190Gly)
c.205C>G (p.Arg69Gly)
4g.42963075C>TCA356792475GRXCR1c.568C>T (p.Arg190Ter)
c.205C>T (p.Arg69Ter)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.42963076G>ACA2904439GRXCR1c.569G>A (p.Arg190Gln)
c.206G>A (p.Arg69Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.42963076G>CCA2904440GRXCR1c.569G>C (p.Arg190Pro)
c.206G>C (p.Arg69Pro)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.42963076G=CA1453073819GRXCR1c.569G= (p.Arg190=)
c.206G= (p.Arg69=)
4g.42963076G>TCA356792477GRXCR1c.569G>T (p.Arg190Leu)
c.206G>T (p.Arg69Leu)
4g.42963077A>CCA439191717GRXCR1c.570A>C (p.Arg190=)
c.207A>C (p.Arg69=)
4g.42963077A>GCA439191718GRXCR1c.570A>G (p.Arg190=)
c.207A>G (p.Arg69=)
4g.42963077A>TCA439191719GRXCR1c.570A>T (p.Arg190=)
c.207A>T (p.Arg69=)
 gnomAD v4
4g.42963078C>ACA439191720GRXCR1c.571C>A (p.Arg191=)
c.208C>A (p.Arg70=)
 COSMIC
4g.42963078C=CA1453073820GRXCR1c.571C= (p.Arg191=)
c.208C= (p.Arg70=)
4g.42963078C>GCA356792478GRXCR1c.571C>G (p.Arg191Gly)
c.208C>G (p.Arg70Gly)
4g.42963078C>TCA2904441GRXCR1c.571C>T (p.Arg191Ter)
c.208C>T (p.Arg70Ter)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.42963079G>ACA356792479GRXCR1c.572G>A (p.Arg191Gln)
c.209G>A (p.Arg70Gln)
 gnomAD v4 COSMIC
4g.42963079G>CCA356792480GRXCR1c.572G>C (p.Arg191Pro)
c.209G>C (p.Arg70Pro)
4g.42963079G>TCA356792481GRXCR1c.572G>T (p.Arg191Leu)
c.209G>T (p.Arg70Leu)
4g.42963080A=CA1453073821GRXCR1c.573A= (p.Arg191=)
c.210A= (p.Arg70=)
4g.42963080A>CCA439191722GRXCR1c.573A>C (p.Arg191=)
c.210A>C (p.Arg70=)
4g.42963080A>GCA2904442GRXCR1c.573A>G (p.Arg191=)
c.210A>G (p.Arg70=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.42963080A>TCA439191723GRXCR1c.573A>T (p.Arg191=)
c.210A>T (p.Arg70=)
4g.42963081G>ACA2904443GRXCR1c.574G>A (p.Val192Ile)
c.211G>A (p.Val71Ile)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.42963081G>CCA2904444GRXCR1c.574G>C (p.Val192Leu)
c.211G>C (p.Val71Leu)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.42963081G=CA1453073822GRXCR1c.574G= (p.Val192=)
c.211G= (p.Val71=)
4g.42963081G>TCA356792482GRXCR1c.574G>T (p.Val192Phe)
c.211G>T (p.Val71Phe)
 COSMIC
4g.42963082T>ACA356792483GRXCR1c.575T>A (p.Val192Asp)
c.212T>A (p.Val71Asp)
4g.42963082T>CCA356792484GRXCR1c.575T>C (p.Val192Ala)
c.212T>C (p.Val71Ala)
4g.42963082T>GCA356792485GRXCR1c.575T>G (p.Val192Gly)
c.212T>G (p.Val71Gly)
4g.42963083T>ACA439191725GRXCR1c.576T>A (p.Val192=)
c.213T>A (p.Val71=)
4g.42963083T>CCA439191726GRXCR1c.576T>C (p.Val192=)
c.213T>C (p.Val71=)
4g.42963083T>GCA439191727GRXCR1c.576T>G (p.Val192=)
c.213T>G (p.Val71=)
4g.42963086_42963097delCA2670496484GRXCR1c.579_590del (p.Glu194_Ser197del)
c.216_227del (p.Glu73_Ser76del)
 gnomAD v4
4g.42963083_42963084insAGAGGGCA2670496485GRXCR1c.576_577insAGAGGG (p.Val192_Ser193insArgGly)
c.213_214insAGAGGG (p.Val71_Ser72insArgGly)
 gnomAD v4
4g.42963084T>ACA356792486GRXCR1c.577T>A (p.Ser193Thr)
c.214T>A (p.Ser72Thr)
4g.42963084T>CCA356792487GRXCR1c.577T>C (p.Ser193Pro)
c.214T>C (p.Ser72Pro)
4g.42963084T>GCA356792488GRXCR1c.577T>G (p.Ser193Ala)
c.214T>G (p.Ser72Ala)
4g.42963085C>ACA356792489GRXCR1c.578C>A (p.Ser193Tyr)
c.215C>A (p.Ser72Tyr)
4g.42963085C>GCA356792490GRXCR1c.578C>G (p.Ser193Cys)
c.215C>G (p.Ser72Cys)
 gnomAD v4
4g.42963085C>TCA356792491GRXCR1c.578C>T (p.Ser193Phe)
c.215C>T (p.Ser72Phe)
4g.42963086T>ACA439191729GRXCR1c.579T>A (p.Ser193=)
c.216T>A (p.Ser72=)
4g.42963086T>CCA96311685GRXCR1c.579T>C (p.Ser193=)
c.216T>C (p.Ser72=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.42963086T>GCA439191728GRXCR1c.579T>G (p.Ser193=)
c.216T>G (p.Ser72=)
4g.42963086T=CA1453073823GRXCR1c.579T= (p.Ser193=)
c.216T= (p.Ser72=)
4g.42963087G>ACA356792492GRXCR1c.580G>A (p.Glu194Lys)
c.217G>A (p.Glu73Lys)
4g.42963087G>CCA356792493GRXCR1c.580G>C (p.Glu194Gln)
c.217G>C (p.Glu73Gln)
4g.42963087G>TCA356792494GRXCR1c.580G>T (p.Glu194Ter)
c.217G>T (p.Glu73Ter)
 COSMIC
4g.42963088A=CA1453073824GRXCR1c.581A= (p.Glu194=)
c.218A= (p.Glu73=)
4g.42963088A>CCA356792497GRXCR1c.581A>C (p.Glu194Ala)
c.218A>C (p.Glu73Ala)
 dbSNP gnomAD v4
4g.42963088A>GCA356792495GRXCR1c.581A>G (p.Glu194Gly)
c.218A>G (p.Glu73Gly)
4g.42963088A>TCA356792496GRXCR1c.581A>T (p.Glu194Val)
c.218A>T (p.Glu73Val)
4g.42963089A>CCA356792498GRXCR1c.582A>C (p.Glu194Asp)
c.219A>C (p.Glu73Asp)
4g.42963089A>GCA439191730GRXCR1c.582A>G (p.Glu194=)
c.219A>G (p.Glu73=)
4g.42963089A>TCA356792499GRXCR1c.582A>T (p.Glu194Asp)
c.219A>T (p.Glu73Asp)
4g.42963089_42963099delCA2670496486GRXCR1c.582_592del (p.Glu194AspfsTer7)
c.219_229del (p.Glu73AspfsTer7)
 gnomAD v4
4g.42963090G>ACA356792500GRXCR1c.583G>A (p.Ala195Thr)
c.220G>A (p.Ala74Thr)
4g.42963090G>CCA356792501GRXCR1c.583G>C (p.Ala195Pro)
c.220G>C (p.Ala74Pro)
4g.42963090G=CA1453073825GRXCR1c.583G= (p.Ala195=)
c.220G= (p.Ala74=)
4g.42963090G>TCA2904445GRXCR1c.583G>T (p.Ala195Ser)
c.220G>T (p.Ala74Ser)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.42963091C>ACA356792502GRXCR1c.584C>A (p.Ala195Asp)
c.221C>A (p.Ala74Asp)
 gnomAD v4
4g.42963091C>GCA356792503GRXCR1c.584C>G (p.Ala195Gly)
c.221C>G (p.Ala74Gly)
4g.42963091C>TCA356792504GRXCR1c.584C>T (p.Ala195Val)
c.221C>T (p.Ala74Val)
4g.42963092T>ACA439191731GRXCR1c.585T>A (p.Ala195=)
c.222T>A (p.Ala74=)
4g.42963092T>CCA439191733GRXCR1c.585T>C (p.Ala195=)
c.222T>C (p.Ala74=)
4g.42963092T>GCA439191732GRXCR1c.585T>G (p.Ala195=)
c.222T>G (p.Ala74=)
4g.42963093C>ACA356792505GRXCR1c.586C>A (p.Pro196Thr)
c.223C>A (p.Pro75Thr)
4g.42963093C=CA1453073826GRXCR1c.586C= (p.Pro196=)
c.223C= (p.Pro75=)
4g.42963093C>GCA356792506GRXCR1c.586C>G (p.Pro196Ala)
c.223C>G (p.Pro75Ala)
4g.42963093C>TCA96311686GRXCR1c.586C>T (p.Pro196Ser)
c.223C>T (p.Pro75Ser)
 dbSNP gnomAD v3 gnomAD v4
4g.42963094C>ACA356792509GRXCR1c.587C>A (p.Pro196His)
c.224C>A (p.Pro75His)
4g.42963094C>GCA356792508GRXCR1c.587C>G (p.Pro196Arg)
c.224C>G (p.Pro75Arg)
4g.42963094C>TCA356792507GRXCR1c.587C>T (p.Pro196Leu)
c.224C>T (p.Pro75Leu)
 COSMIC
4g.42963095T>ACA439191734GRXCR1c.588T>A (p.Pro196=)
c.225T>A (p.Pro75=)
4g.42963095T>CCA439191735GRXCR1c.588T>C (p.Pro196=)
c.225T>C (p.Pro75=)
 gnomAD v4
4g.42963095T>GCA439191736GRXCR1c.588T>G (p.Pro196=)
c.225T>G (p.Pro75=)
4g.42963095T=CA1453073827GRXCR1c.588T= (p.Pro196=)
c.225T= (p.Pro75=)

Number of alleles fetched