Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.154039566A>CCA366152304OPRM1c.22A>C (p.Thr8Pro)
c.208A>C (p.Thr70Pro)
c.301A>C (p.Thr101Pro)
c.47+29007A>C (p.=)
c.166A>C (p.Thr56Pro)
c.-11+28548A>C (p.=)
6g.154039566A>GCA366152305OPRM1c.22A>G (p.Thr8Ala)
c.208A>G (p.Thr70Ala)
c.301A>G (p.Thr101Ala)
c.47+29007A>G (p.=)
c.166A>G (p.Thr56Ala)
c.-11+28548A>G (p.=)
6g.154039566A>TCA366152306OPRM1c.22A>T (p.Thr8Ser)
c.208A>T (p.Thr70Ser)
c.301A>T (p.Thr101Ser)
c.47+29007A>T (p.=)
c.166A>T (p.Thr56Ser)
c.-11+28548A>T (p.=)
6g.154039567C>ACA366152307OPRM1c.23C>A (p.Thr8Lys)
c.209C>A (p.Thr70Lys)
c.302C>A (p.Thr101Lys)
c.47+29008C>A (p.=)
c.167C>A (p.Thr56Lys)
c.-11+28549C>A (p.=)
6g.154039567C>GCA366152308OPRM1c.23C>G (p.Thr8Arg)
c.209C>G (p.Thr70Arg)
c.302C>G (p.Thr101Arg)
c.47+29008C>G (p.=)
c.167C>G (p.Thr56Arg)
c.-11+28549C>G (p.=)
6g.154039567C>TCA366152309OPRM1c.23C>T (p.Thr8Met)
c.209C>T (p.Thr70Met)
c.302C>T (p.Thr101Met)
c.47+29008C>T (p.=)
c.167C>T (p.Thr56Met)
c.-11+28549C>T (p.=)
6g.154039568G>ACA150238740OPRM1c.24G>A (p.Thr8=)
c.210G>A (p.Thr70=)
c.303G>A (p.Thr101=)
c.47+29009G>A (p.=)
c.168G>A (p.Thr56=)
c.-11+28550G>A (p.=)
dbSNP gnomAD COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
6g.154039568G>CCA452973652OPRM1c.24G>C (p.Thr8=)
c.210G>C (p.Thr70=)
c.303G>C (p.Thr101=)
c.47+29009G>C (p.=)
c.168G>C (p.Thr56=)
c.-11+28550G>C (p.=)
6g.154039568G>TCA452973653OPRM1c.24G>T (p.Thr8=)
c.210G>T (p.Thr70=)
c.303G>T (p.Thr101=)
c.47+29009G>T (p.=)
c.168G>T (p.Thr56=)
c.-11+28550G>T (p.=)
6g.154039569A>CCA366152310OPRM1c.25A>C (p.Asn9His)
c.211A>C (p.Asn71His)
c.304A>C (p.Asn102His)
c.47+29010A>C (p.=)
c.169A>C (p.Asn57His)
c.-11+28551A>C (p.=)
6g.154039569A>GCA366152311OPRM1c.25A>G (p.Asn9Asp)
c.211A>G (p.Asn71Asp)
c.304A>G (p.Asn102Asp)
c.47+29010A>G (p.=)
c.169A>G (p.Asn57Asp)
c.-11+28551A>G (p.=)
gnomAD
6g.154039569A>TCA366152312OPRM1c.25A>T (p.Asn9Tyr)
c.211A>T (p.Asn71Tyr)
c.304A>T (p.Asn102Tyr)
c.47+29010A>T (p.=)
c.169A>T (p.Asn57Tyr)
c.-11+28551A>T (p.=)
6g.154039570A>CCA366152315OPRM1c.26A>C (p.Asn9Thr)
c.212A>C (p.Asn71Thr)
c.305A>C (p.Asn102Thr)
c.47+29011A>C (p.=)
c.170A>C (p.Asn57Thr)
c.-11+28552A>C (p.=)
6g.154039570A>GCA366152314OPRM1c.26A>G (p.Asn9Ser)
c.212A>G (p.Asn71Ser)
c.305A>G (p.Asn102Ser)
c.47+29011A>G (p.=)
c.170A>G (p.Asn57Ser)
c.-11+28552A>G (p.=)
6g.154039570A>TCA366152313OPRM1c.26A>T (p.Asn9Ile)
c.212A>T (p.Asn71Ile)
c.305A>T (p.Asn102Ile)
c.47+29011A>T (p.=)
c.170A>T (p.Asn57Ile)
c.-11+28552A>T (p.=)
6g.154039571C>ACA4061351OPRM1c.27C>A (p.Asn9Lys)
c.213C>A (p.Asn71Lys)
c.306C>A (p.Asn102Lys)
c.47+29012C>A (p.=)
c.171C>A (p.Asn57Lys)
c.-11+28553C>A (p.=)
dbSNP ExAC gnomAD
6g.154039571C>GCA4061353OPRM1c.27C>G (p.Asn9Lys)
c.213C>G (p.Asn71Lys)
c.306C>G (p.Asn102Lys)
c.47+29012C>G (p.=)
c.171C>G (p.Asn57Lys)
c.-11+28553C>G (p.=)
dbSNP ExAC gnomAD
6g.154039571C>TCA4061352OPRM1c.27C>T (p.Asn9=)
c.213C>T (p.Asn71=)
c.306C>T (p.Asn102=)
c.47+29012C>T (p.=)
c.171C>T (p.Asn57=)
c.-11+28553C>T (p.=)
ClinVar dbSNP ExAC gnomAD
6g.154039572G>ACA366152316OPRM1c.28G>A (p.Ala10Thr)
c.214G>A (p.Ala72Thr)
c.307G>A (p.Ala103Thr)
c.47+29013G>A (p.=)
c.172G>A (p.Ala58Thr)
c.-11+28554G>A (p.=)
gnomAD
6g.154039572G>CCA366152317OPRM1c.28G>C (p.Ala10Pro)
c.214G>C (p.Ala72Pro)
c.307G>C (p.Ala103Pro)
c.47+29013G>C (p.=)
c.172G>C (p.Ala58Pro)
c.-11+28554G>C (p.=)
6g.154039572G>TCA366152318OPRM1c.28G>T (p.Ala10Ser)
c.214G>T (p.Ala72Ser)
c.307G>T (p.Ala103Ser)
c.47+29013G>T (p.=)
c.172G>T (p.Ala58Ser)
c.-11+28554G>T (p.=)
6g.154039573C>ACA4061354OPRM1c.29C>A (p.Ala10Asp)
c.215C>A (p.Ala72Asp)
c.308C>A (p.Ala103Asp)
c.47+29014C>A (p.=)
c.173C>A (p.Ala58Asp)
c.-11+28555C>A (p.=)
dbSNP ExAC gnomAD
6g.154039573C>GCA366152319OPRM1c.29C>G (p.Ala10Gly)
c.215C>G (p.Ala72Gly)
c.308C>G (p.Ala103Gly)
c.47+29014C>G (p.=)
c.173C>G (p.Ala58Gly)
c.-11+28555C>G (p.=)
6g.154039573C>TCA366152320OPRM1c.29C>T (p.Ala10Val)
c.215C>T (p.Ala72Val)
c.308C>T (p.Ala103Val)
c.47+29014C>T (p.=)
c.173C>T (p.Ala58Val)
c.-11+28555C>T (p.=)
6g.154039574C>ACA452973654OPRM1c.30C>A (p.Ala10=)
c.216C>A (p.Ala72=)
c.309C>A (p.Ala103=)
c.47+29015C>A (p.=)
c.174C>A (p.Ala58=)
c.-11+28556C>A (p.=)
6g.154039574C>GCA452973655OPRM1c.30C>G (p.Ala10=)
c.216C>G (p.Ala72=)
c.309C>G (p.Ala103=)
c.47+29015C>G (p.=)
c.174C>G (p.Ala58=)
c.-11+28556C>G (p.=)
6g.154039574C>TCA452973656OPRM1c.30C>T (p.Ala10=)
c.216C>T (p.Ala72=)
c.309C>T (p.Ala103=)
c.47+29015C>T (p.=)
c.174C>T (p.Ala58=)
c.-11+28556C>T (p.=)
6g.154039575A>CCA366152321OPRM1c.31A>C (p.Ser11Arg)
c.217A>C (p.Ser73Arg)
c.310A>C (p.Ser104Arg)
c.47+29016A>C (p.=)
c.175A>C (p.Ser59Arg)
c.-11+28557A>C (p.=)
6g.154039575A>GCA366152322OPRM1c.31A>G (p.Ser11Gly)
c.217A>G (p.Ser73Gly)
c.310A>G (p.Ser104Gly)
c.47+29016A>G (p.=)
c.175A>G (p.Ser59Gly)
c.-11+28557A>G (p.=)
6g.154039575A>TCA366152323OPRM1c.31A>T (p.Ser11Cys)
c.217A>T (p.Ser73Cys)
c.310A>T (p.Ser104Cys)
c.47+29016A>T (p.=)
c.175A>T (p.Ser59Cys)
c.-11+28557A>T (p.=)
6g.154039576G>ACA366152326OPRM1c.32G>A (p.Ser11Asn)
c.218G>A (p.Ser73Asn)
c.311G>A (p.Ser104Asn)
c.47+29017G>A (p.=)
c.176G>A (p.Ser59Asn)
c.-11+28558G>A (p.=)
6g.154039576G>CCA366152325OPRM1c.32G>C (p.Ser11Thr)
c.218G>C (p.Ser73Thr)
c.311G>C (p.Ser104Thr)
c.47+29017G>C (p.=)
c.176G>C (p.Ser59Thr)
c.-11+28558G>C (p.=)
6g.154039576G>TCA366152324OPRM1c.32G>T (p.Ser11Ile)
c.218G>T (p.Ser73Ile)
c.311G>T (p.Ser104Ile)
c.47+29017G>T (p.=)
c.176G>T (p.Ser59Ile)
c.-11+28558G>T (p.=)
6g.154039576_154039577delCA821046617OPRM1c.32_33del (p.Ser11LysfsTer4)
c.218_219del (p.Ser73LysfsTer4)
c.311_312del (p.Ser104LysfsTer4)
c.47+29017_47+29018del (p.=)
c.176_177del (p.Ser59LysfsTer4)
c.-11+28558_-11+28559del (p.=)
dbSNP
6g.154039577C>ACA366152327OPRM1c.33C>A (p.Ser11Arg)
c.219C>A (p.Ser73Arg)
c.312C>A (p.Ser104Arg)
c.47+29018C>A (p.=)
c.177C>A (p.Ser59Arg)
c.-11+28559C>A (p.=)
6g.154039577C>GCA366152328OPRM1c.33C>G (p.Ser11Arg)
c.219C>G (p.Ser73Arg)
c.312C>G (p.Ser104Arg)
c.47+29018C>G (p.=)
c.177C>G (p.Ser59Arg)
c.-11+28559C>G (p.=)
6g.154039577C>TCA452973660OPRM1c.33C>T (p.Ser11=)
c.219C>T (p.Ser73=)
c.312C>T (p.Ser104=)
c.47+29018C>T (p.=)
c.177C>T (p.Ser59=)
c.-11+28559C>T (p.=)
6g.154039578A>CCA366152329OPRM1c.34A>C (p.Asn12His)
c.220A>C (p.Asn74His)
c.313A>C (p.Asn105His)
c.47+29019A>C (p.=)
c.178A>C (p.Asn60His)
c.-11+28560A>C (p.=)
6g.154039578A>GCA366152330OPRM1c.34A>G (p.Asn12Asp)
c.220A>G (p.Asn74Asp)
c.313A>G (p.Asn105Asp)
c.47+29019A>G (p.=)
c.178A>G (p.Asn60Asp)
c.-11+28560A>G (p.=)
6g.154039578A>TCA366152331OPRM1c.34A>T (p.Asn12Tyr)
c.220A>T (p.Asn74Tyr)
c.313A>T (p.Asn105Tyr)
c.47+29019A>T (p.=)
c.178A>T (p.Asn60Tyr)
c.-11+28560A>T (p.=)
6g.154039579A>CCA366152332OPRM1c.35A>C (p.Asn12Thr)
c.221A>C (p.Asn74Thr)
c.314A>C (p.Asn105Thr)
c.47+29020A>C (p.=)
c.179A>C (p.Asn60Thr)
c.-11+28561A>C (p.=)
6g.154039579A>GCA150238793OPRM1c.35A>G (p.Asn12Ser)
c.221A>G (p.Asn74Ser)
c.314A>G (p.Asn105Ser)
c.47+29020A>G (p.=)
c.179A>G (p.Asn60Ser)
c.-11+28561A>G (p.=)
dbSNP
6g.154039579A>TCA150238808OPRM1c.35A>T (p.Asn12Ile)
c.221A>T (p.Asn74Ile)
c.314A>T (p.Asn105Ile)
c.47+29020A>T (p.=)
c.179A>T (p.Asn60Ile)
c.-11+28561A>T (p.=)
dbSNP
6g.154039580T>ACA366152333OPRM1c.36T>A (p.Asn12Lys)
c.222T>A (p.Asn74Lys)
c.315T>A (p.Asn105Lys)
c.47+29021T>A (p.=)
c.180T>A (p.Asn60Lys)
c.-11+28562T>A (p.=)
6g.154039580T>CCA452973662OPRM1c.36T>C (p.Asn12=)
c.222T>C (p.Asn74=)
c.315T>C (p.Asn105=)
c.47+29021T>C (p.=)
c.180T>C (p.Asn60=)
c.-11+28562T>C (p.=)
6g.154039580T>GCA366152334OPRM1c.36T>G (p.Asn12Lys)
c.222T>G (p.Asn74Lys)
c.315T>G (p.Asn105Lys)
c.47+29021T>G (p.=)
c.180T>G (p.Asn60Lys)
c.-11+28562T>G (p.=)
6g.154039581T>ACA366152335OPRM1c.37T>A (p.Cys13Ser)
c.223T>A (p.Cys75Ser)
c.316T>A (p.Cys106Ser)
c.47+29022T>A (p.=)
c.181T>A (p.Cys61Ser)
c.-11+28563T>A (p.=)
6g.154039581T>CCA366152336OPRM1c.37T>C (p.Cys13Arg)
c.223T>C (p.Cys75Arg)
c.316T>C (p.Cys106Arg)
c.47+29022T>C (p.=)
c.181T>C (p.Cys61Arg)
c.-11+28563T>C (p.=)
6g.154039581T>GCA4061355OPRM1c.37T>G (p.Cys13Gly)
c.223T>G (p.Cys75Gly)
c.316T>G (p.Cys106Gly)
c.47+29022T>G (p.=)
c.181T>G (p.Cys61Gly)
c.-11+28563T>G (p.=)
dbSNP ExAC gnomAD
6g.154039582G>ACA366152337OPRM1c.38G>A (p.Cys13Tyr)
c.224G>A (p.Cys75Tyr)
c.317G>A (p.Cys106Tyr)
c.47+29023G>A (p.=)
c.182G>A (p.Cys61Tyr)
c.-11+28564G>A (p.=)

Number of alleles fetched