Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.46892483A>CCA388152876HTR2Ac.520T>G (p.Tyr174Asp)
c.31T>G (p.Tyr11Asp)
c.268T>G (p.Tyr90Asp)
13g.46892483A>GCA388152877HTR2Ac.520T>C (p.Tyr174His)
c.31T>C (p.Tyr11His)
c.268T>C (p.Tyr90His)
13g.46892483A>TCA388152879HTR2Ac.520T>A (p.Tyr174Asn)
c.31T>A (p.Tyr11Asn)
c.268T>A (p.Tyr90Asn)
13g.46892484G>ACA483554994HTR2Ac.519C>T (p.Arg173=)
c.30C>T (p.Arg10=)
c.267C>T (p.Arg89=)
13g.46892484G>CCA483554995HTR2Ac.519C>G (p.Arg173=)
c.30C>G (p.Arg10=)
c.267C>G (p.Arg89=)
13g.46892484G>TCA483554996HTR2Ac.519C>A (p.Arg173=)
c.30C>A (p.Arg10=)
c.267C>A (p.Arg89=)
13g.46892485C>ACA388152882HTR2Ac.518G>T (p.Arg173Leu)
c.29G>T (p.Arg10Leu)
c.266G>T (p.Arg89Leu)
13g.46892485C=CA2089308757HTR2Ac.518G= (p.Arg173=)
c.29G= (p.Arg10=)
c.266G= (p.Arg89=)
13g.46892485C>GCA388152884HTR2Ac.518G>C (p.Arg173Pro)
c.29G>C (p.Arg10Pro)
c.266G>C (p.Arg89Pro)
13g.46892485C>TCA388152885HTR2Ac.518G>A (p.Arg173His)
c.29G>A (p.Arg10His)
c.266G>A (p.Arg89His)
 dbSNP gnomAD v2 gnomAD v4
13g.46892486G>ACA6977638HTR2Ac.517C>T (p.Arg173Cys)
c.28C>T (p.Arg10Cys)
c.265C>T (p.Arg89Cys)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.46892486G>CCA388152889HTR2Ac.517C>G (p.Arg173Gly)
c.28C>G (p.Arg10Gly)
c.265C>G (p.Arg89Gly)
13g.46892486G=CA2089308761HTR2Ac.517C= (p.Arg173=)
c.28C= (p.Arg10=)
c.265C= (p.Arg89=)
13g.46892486G>TCA388152890HTR2Ac.517C>A (p.Arg173Ser)
c.28C>A (p.Arg10Ser)
c.265C>A (p.Arg89Ser)
13g.46892487G>ACA6977639HTR2Ac.516C>T (p.Asp172=)
c.27C>T (p.Asp9=)
c.264C>T (p.Asp88=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.46892487G>CCA388152895HTR2Ac.516C>G (p.Asp172Glu)
c.27C>G (p.Asp9Glu)
c.264C>G (p.Asp88Glu)
13g.46892487G=CA1630855947HTR2Ac.516C= (p.Asp172=)
c.27C= (p.Asp9=)
c.264C= (p.Asp88=)
13g.46892487G>TCA388152892HTR2Ac.516C>A (p.Asp172Glu)
c.27C>A (p.Asp9Glu)
c.264C>A (p.Asp88Glu)
13g.46892488T>ACA388152899HTR2Ac.515A>T (p.Asp172Val)
c.26A>T (p.Asp9Val)
c.263A>T (p.Asp88Val)
13g.46892488T>CCA388152896HTR2Ac.515A>G (p.Asp172Gly)
c.26A>G (p.Asp9Gly)
c.263A>G (p.Asp88Gly)
13g.46892488T>GCA388152898HTR2Ac.515A>C (p.Asp172Ala)
c.26A>C (p.Asp9Ala)
c.263A>C (p.Asp88Ala)
 dbSNP COSMIC
13g.46892488T=CA2089308766HTR2Ac.515A= (p.Asp172=)
c.26A= (p.Asp9=)
c.263A= (p.Asp88=)
13g.46892489C>ACA388152901HTR2Ac.514G>T (p.Asp172Tyr)
c.25G>T (p.Asp9Tyr)
c.262G>T (p.Asp88Tyr)
13g.46892489C>GCA388152902HTR2Ac.514G>C (p.Asp172His)
c.25G>C (p.Asp9His)
c.262G>C (p.Asp88His)
13g.46892489C>TCA388152904HTR2Ac.514G>A (p.Asp172Asn)
c.25G>A (p.Asp9Asn)
c.262G>A (p.Asp88Asn)
 gnomAD v4
13g.46892490C>ACA483554997HTR2Ac.513G>T (p.Leu171=)
c.24G>T (p.Leu8=)
c.261G>T (p.Leu87=)
13g.46892490C>GCA483554998HTR2Ac.513G>C (p.Leu171=)
c.24G>C (p.Leu8=)
c.261G>C (p.Leu87=)
13g.46892490C>TCA483554999HTR2Ac.513G>A (p.Leu171=)
c.24G>A (p.Leu8=)
c.261G>A (p.Leu87=)
13g.46892491A>CCA388152906HTR2Ac.512T>G (p.Leu171Arg)
c.23T>G (p.Leu8Arg)
c.260T>G (p.Leu87Arg)
13g.46892491A>GCA388152908HTR2Ac.512T>C (p.Leu171Pro)
c.23T>C (p.Leu8Pro)
c.260T>C (p.Leu87Pro)
13g.46892491A>TCA388152910HTR2Ac.512T>A (p.Leu171Gln)
c.23T>A (p.Leu8Gln)
c.260T>A (p.Leu87Gln)
13g.46892492G>ACA483555000HTR2Ac.511C>T (p.Leu171=)
c.22C>T (p.Leu8=)
c.259C>T (p.Leu87=)
 gnomAD v4
13g.46892492G>CCA388152912HTR2Ac.511C>G (p.Leu171Val)
c.22C>G (p.Leu8Val)
c.259C>G (p.Leu87Val)
13g.46892492G>TCA388152914HTR2Ac.511C>A (p.Leu171Met)
c.22C>A (p.Leu8Met)
c.259C>A (p.Leu87Met)
13g.46892493C>ACA483555001HTR2Ac.510G>T (p.Ser170=)
c.21G>T (p.Ser7=)
c.258G>T (p.Ser86=)
 dbSNP gnomAD v2 gnomAD v4
13g.46892493C=CA2089308769HTR2Ac.510G= (p.Ser170=)
c.21G= (p.Ser7=)
c.258G= (p.Ser86=)
13g.46892493C>GCA483555002HTR2Ac.510G>C (p.Ser170=)
c.21G>C (p.Ser7=)
c.258G>C (p.Ser86=)
13g.46892493C>TCA6977640HTR2Ac.510G>A (p.Ser170=)
c.21G>A (p.Ser7=)
c.258G>A (p.Ser86=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
13g.46892494G>ACA388152923HTR2Ac.509C>T (p.Ser170Leu)
c.20C>T (p.Ser7Leu)
c.257C>T (p.Ser86Leu)
 dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC
13g.46892494G>CCA388152921HTR2Ac.509C>G (p.Ser170Trp)
c.20C>G (p.Ser7Trp)
c.257C>G (p.Ser86Trp)
13g.46892494G=CA2089308772HTR2Ac.509C= (p.Ser170=)
c.20C= (p.Ser7=)
c.257C= (p.Ser86=)
13g.46892494G>TCA388152919HTR2Ac.509C>A (p.Ser170Ter)
c.20C>A (p.Ser7Ter)
c.257C>A (p.Ser86Ter)
13g.46892495A>CCA388152925HTR2Ac.508T>G (p.Ser170Ala)
c.19T>G (p.Ser7Ala)
c.256T>G (p.Ser86Ala)
13g.46892495A>GCA388152927HTR2Ac.508T>C (p.Ser170Pro)
c.19T>C (p.Ser7Pro)
c.256T>C (p.Ser86Pro)
13g.46892495A>TCA388152929HTR2Ac.508T>A (p.Ser170Thr)
c.19T>A (p.Ser7Thr)
c.256T>A (p.Ser86Thr)
13g.46892496G>ACA483555003HTR2Ac.507C>T (p.Ile169=)
c.18C>T (p.Ile6=)
c.255C>T (p.Ile85=)
13g.46892496G>CCA388152931HTR2Ac.507C>G (p.Ile169Met)
c.18C>G (p.Ile6Met)
c.255C>G (p.Ile85Met)
13g.46892496G>TCA483555004HTR2Ac.507C>A (p.Ile169=)
c.18C>A (p.Ile6=)
c.255C>A (p.Ile85=)
13g.46892497A>CCA388152934HTR2Ac.506T>G (p.Ile169Ser)
c.17T>G (p.Ile6Ser)
c.254T>G (p.Ile85Ser)
13g.46892497A>GCA388152936HTR2Ac.506T>C (p.Ile169Thr)
c.17T>C (p.Ile6Thr)
c.254T>C (p.Ile85Thr)
 gnomAD v4
13g.46892497A>TCA388152938HTR2Ac.506T>A (p.Ile169Asn)
c.17T>A (p.Ile6Asn)
c.254T>A (p.Ile85Asn)
13g.46892498T>ACA388152940HTR2Ac.505A>T (p.Ile169Phe)
c.16A>T (p.Ile6Phe)
c.253A>T (p.Ile85Phe)
13g.46892498T>CCA388152942HTR2Ac.505A>G (p.Ile169Val)
c.16A>G (p.Ile6Val)
c.253A>G (p.Ile85Val)
13g.46892498T>GCA388152945HTR2Ac.505A>C (p.Ile169Leu)
c.16A>C (p.Ile6Leu)
c.253A>C (p.Ile85Leu)
13g.46892499G>ACA483555007HTR2Ac.504C>T (p.Ala168=)
c.15C>T (p.Ala5=)
c.252C>T (p.Ala84=)
 gnomAD v4 COSMIC COSMIC
13g.46892499G>CCA483555006HTR2Ac.504C>G (p.Ala168=)
c.15C>G (p.Ala5=)
c.252C>G (p.Ala84=)
13g.46892499G>TCA483555005HTR2Ac.504C>A (p.Ala168=)
c.15C>A (p.Ala5=)
c.252C>A (p.Ala84=)
13g.46892500G>ACA388152947HTR2Ac.503C>T (p.Ala168Val)
c.14C>T (p.Ala5Val)
c.251C>T (p.Ala84Val)
13g.46892500G>CCA388152949HTR2Ac.503C>G (p.Ala168Gly)
c.14C>G (p.Ala5Gly)
c.251C>G (p.Ala84Gly)
13g.46892500G>TCA388152951HTR2Ac.503C>A (p.Ala168Asp)
c.14C>A (p.Ala5Asp)
c.251C>A (p.Ala84Asp)
13g.46892501C>ACA388152953HTR2Ac.502G>T (p.Ala168Ser)
c.13G>T (p.Ala5Ser)
c.250G>T (p.Ala84Ser)
13g.46892501C=CA2089308774HTR2Ac.502G= (p.Ala168=)
c.13G= (p.Ala5=)
c.250G= (p.Ala84=)
13g.46892501C>GCA388152954HTR2Ac.502G>C (p.Ala168Pro)
c.13G>C (p.Ala5Pro)
c.250G>C (p.Ala84Pro)
13g.46892501C>TCA6977641HTR2Ac.502G>A (p.Ala168Thr)
c.13G>A (p.Ala5Thr)
c.250G>A (p.Ala84Thr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
13g.46892502G>ACA6977642HTR2Ac.501C>T (p.Cys167=)
c.12C>T (p.Cys4=)
c.249C>T (p.Cys83=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.46892502G>CCA388152957HTR2Ac.501C>G (p.Cys167Trp)
c.12C>G (p.Cys4Trp)
c.249C>G (p.Cys83Trp)
13g.46892502G=CA2089308777HTR2Ac.501C= (p.Cys167=)
c.12C= (p.Cys4=)
c.249C= (p.Cys83=)
13g.46892502G>TCA388152959HTR2Ac.501C>A (p.Cys167Ter)
c.12C>A (p.Cys4Ter)
c.249C>A (p.Cys83Ter)
13g.46892503C>ACA388152961HTR2Ac.500G>T (p.Cys167Phe)
c.11G>T (p.Cys4Phe)
c.248G>T (p.Cys83Phe)
13g.46892503C>GCA388152963HTR2Ac.500G>C (p.Cys167Ser)
c.11G>C (p.Cys4Ser)
c.248G>C (p.Cys83Ser)
13g.46892503C>TCA388152965HTR2Ac.500G>A (p.Cys167Tyr)
c.11G>A (p.Cys4Tyr)
c.248G>A (p.Cys83Tyr)
13g.46892504A>CCA388152967HTR2Ac.499T>G (p.Cys167Gly)
c.10T>G (p.Cys4Gly)
c.247T>G (p.Cys83Gly)
 gnomAD v4
13g.46892504A>GCA388152969HTR2Ac.499T>C (p.Cys167Arg)
c.10T>C (p.Cys4Arg)
c.247T>C (p.Cys83Arg)
13g.46892504A>TCA388152971HTR2Ac.499T>A (p.Cys167Ser)
c.10T>A (p.Cys4Ser)
c.247T>A (p.Cys83Ser)
13g.46892505G>ACA483555008HTR2Ac.498C>T (p.Leu166=)
c.9C>T (p.Leu3=)
c.246C>T (p.Leu82=)
13g.46892505G>CCA6977643HTR2Ac.498C>G (p.Leu166=)
c.9C>G (p.Leu3=)
c.246C>G (p.Leu82=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.46892505G=CA2089308779HTR2Ac.498C= (p.Leu166=)
c.9C= (p.Leu3=)
c.246C= (p.Leu82=)
13g.46892505G>TCA483555009HTR2Ac.498C>A (p.Leu166=)
c.9C>A (p.Leu3=)
c.246C>A (p.Leu82=)
13g.46892506A>CCA388152974HTR2Ac.497T>G (p.Leu166Arg)
c.8T>G (p.Leu3Arg)
c.245T>G (p.Leu82Arg)
13g.46892506A>GCA388152977HTR2Ac.497T>C (p.Leu166Pro)
c.8T>C (p.Leu3Pro)
c.245T>C (p.Leu82Pro)
13g.46892506A>TCA388152979HTR2Ac.497T>A (p.Leu166His)
c.8T>A (p.Leu3His)
c.245T>A (p.Leu82His)
13g.46892507G>ACA388152982HTR2Ac.496C>T (p.Leu166Phe)
c.7C>T (p.Leu3Phe)
c.244C>T (p.Leu82Phe)
13g.46892507G>CCA388152984HTR2Ac.496C>G (p.Leu166Val)
c.7C>G (p.Leu3Val)
c.244C>G (p.Leu82Val)
13g.46892507G>TCA388152980HTR2Ac.496C>A (p.Leu166Ile)
c.7C>A (p.Leu3Ile)
c.244C>A (p.Leu82Ile)
13g.46892508G>ACA6977644HTR2Ac.495C>T (p.His165=)
c.6C>T (p.His2=)
c.243C>T (p.His81=)
 dbSNP ExAC gnomAD v2
13g.46892508G>CCA388152987HTR2Ac.495C>G (p.His165Gln)
c.6C>G (p.His2Gln)
c.243C>G (p.His81Gln)
13g.46892508G=CA2089308781HTR2Ac.495C= (p.His165=)
c.6C= (p.His2=)
c.243C= (p.His81=)
13g.46892508G>TCA388152990HTR2Ac.495C>A (p.His165Gln)
c.6C>A (p.His2Gln)
c.243C>A (p.His81Gln)
13g.46892509T>ACA388152992HTR2Ac.494A>T (p.His165Leu)
c.5A>T (p.His2Leu)
c.242A>T (p.His81Leu)
13g.46892509T>CCA388152993HTR2Ac.494A>G (p.His165Arg)
c.5A>G (p.His2Arg)
c.242A>G (p.His81Arg)
 gnomAD v4
13g.46892509T>GCA388152995HTR2Ac.494A>C (p.His165Pro)
c.5A>C (p.His2Pro)
c.242A>C (p.His81Pro)
 dbSNP
13g.46892509T=CA2089308785HTR2Ac.494A= (p.His165=)
c.5A= (p.His2=)
c.242A= (p.His81=)
13g.46892510G>ACA388153002HTR2Ac.493C>T (p.His165Tyr)
c.4C>T (p.His2Tyr)
c.241C>T (p.His81Tyr)
13g.46892510G>CCA388152998HTR2Ac.493C>G (p.His165Asp)
c.4C>G (p.His2Asp)
c.241C>G (p.His81Asp)
13g.46892510G>TCA388153000HTR2Ac.493C>A (p.His165Asn)
c.4C>A (p.His2Asn)
c.241C>A (p.His81Asn)
13g.46892511C>ACA388153007HTR2Ac.492G>T (p.Met164Ile)
c.3G>T (p.Met1Ile)
c.240G>T (p.Met80Ile)
13g.46892511C>GCA388153008HTR2Ac.492G>C (p.Met164Ile)
c.3G>C (p.Met1Ile)
c.240G>C (p.Met80Ile)
13g.46892511C>TCA388153011HTR2Ac.492G>A (p.Met164Ile)
c.3G>A (p.Met1Ile)
c.240G>A (p.Met80Ile)
13g.46892512A>CCA388153014HTR2Ac.491T>G (p.Met164Arg)
c.2T>G (p.Met1Arg)
c.239T>G (p.Met80Arg)
 gnomAD v4
13g.46892512A>GCA388153015HTR2Ac.491T>C (p.Met164Thr)
c.2T>C (p.Met1Thr)
c.239T>C (p.Met80Thr)
 gnomAD v4
13g.46892512A>TCA388153017HTR2Ac.491T>A (p.Met164Lys)
c.2T>A (p.Met1Lys)
c.239T>A (p.Met80Lys)
13g.46892513T>ACA388153021HTR2Ac.490A>T (p.Met164Leu)
c.1A>T (p.Met1Leu)
c.238A>T (p.Met80Leu)
13g.46892513T>CCA388153022HTR2Ac.490A>G (p.Met164Val)
c.1A>G (p.Met1Val)
c.238A>G (p.Met80Val)
13g.46892513T>GCA388153019HTR2Ac.490A>C (p.Met164Leu)
c.1A>C (p.Met1Leu)
c.238A>C (p.Met80Leu)
13g.46892514G>ACA483555011HTR2Ac.489C>T (p.Ile163=)
c.-1C>T (n.-1C>T)
c.237C>T (p.Ile79=)
13g.46892514G>CCA388153024HTR2Ac.489C>G (p.Ile163Met)
c.-1C>G (n.-1C>G)
c.237C>G (p.Ile79Met)
13g.46892514G>TCA483555010HTR2Ac.489C>A (p.Ile163=)
c.-1C>A (n.-1C>A)
c.237C>A (p.Ile79=)
13g.46892515A>CCA388153028HTR2Ac.488T>G (p.Ile163Ser)
c.-2T>G (n.-2T>G)
c.236T>G (p.Ile79Ser)
13g.46892515A>GCA388153027HTR2Ac.488T>C (p.Ile163Thr)
c.-2T>C (n.-2T>C)
c.236T>C (p.Ile79Thr)
 gnomAD v4
13g.46892515A>TCA388153030HTR2Ac.488T>A (p.Ile163Asn)
c.-2T>A (n.-2T>A)
c.236T>A (p.Ile79Asn)
13g.46892516T>ACA388153032HTR2Ac.487A>T (p.Ile163Phe)
c.-3A>T (n.-3A>T)
c.235A>T (p.Ile79Phe)
13g.46892516T>CCA388153036HTR2Ac.487A>G (p.Ile163Val)
c.-3A>G (n.-3A>G)
c.235A>G (p.Ile79Val)
13g.46892516T>GCA388153034HTR2Ac.487A>C (p.Ile163Leu)
c.-3A>C (n.-3A>C)
c.235A>C (p.Ile79Leu)
13g.46892517G>ACA483555012HTR2Ac.486C>T (p.Ser162=)
c.-4C>T (n.-4C>T)
c.234C>T (p.Ser78=)
13g.46892517G>CCA483555013HTR2Ac.486C>G (p.Ser162=)
c.-4C>G (n.-4C>G)
c.234C>G (p.Ser78=)
13g.46892517G>TCA483555014HTR2Ac.486C>A (p.Ser162=)
c.-4C>A (n.-4C>A)
c.234C>A (p.Ser78=)
13g.46892518G>ACA388153038HTR2Ac.485C>T (p.Ser162Phe)
c.-5C>T (n.-5C>T)
c.233C>T (p.Ser78Phe)
13g.46892518G>CCA388153040HTR2Ac.485C>G (p.Ser162Cys)
c.-5C>G (n.-5C>G)
c.233C>G (p.Ser78Cys)
13g.46892518G>TCA388153041HTR2Ac.485C>A (p.Ser162Tyr)
c.-5C>A (n.-5C>A)
c.233C>A (p.Ser78Tyr)
13g.46892519A>CCA388153044HTR2Ac.484T>G (p.Ser162Ala)
c.-6T>G (n.-6T>G)
c.232T>G (p.Ser78Ala)
13g.46892519A>GCA388153046HTR2Ac.484T>C (p.Ser162Pro)
c.-6T>C (n.-6T>C)
c.232T>C (p.Ser78Pro)
 COSMIC
13g.46892519A>TCA388153048HTR2Ac.484T>A (p.Ser162Thr)
c.-6T>A (n.-6T>A)
c.232T>A (p.Ser78Thr)
13g.46892520G>ACA6977645HTR2Ac.483C>T (p.Ala161=)
c.-7C>T (n.-7C>T)
c.231C>T (p.Ala77=)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.46892520G>CCA483555015HTR2Ac.483C>G (p.Ala161=)
c.-7C>G (n.-7C>G)
c.231C>G (p.Ala77=)
13g.46892520G=CA2089308788HTR2Ac.483C= (p.Ala161=)
c.-7C= (n.-7C=)
c.231C= (p.Ala77=)
13g.46892520G>TCA483555016HTR2Ac.483C>A (p.Ala161=)
c.-7C>A (n.-7C>A)
c.231C>A (p.Ala77=)
13g.46892521G>ACA388153053HTR2Ac.482C>T (p.Ala161Val)
c.-8C>T (n.-8C>T)
c.230C>T (p.Ala77Val)
13g.46892521G>CCA388153055HTR2Ac.482C>G (p.Ala161Gly)
c.-8C>G (n.-8C>G)
c.230C>G (p.Ala77Gly)
13g.46892521G>TCA388153058HTR2Ac.482C>A (p.Ala161Asp)
c.-8C>A (n.-8C>A)
c.230C>A (p.Ala77Asp)
13g.46892522C>ACA388153060HTR2Ac.481G>T (p.Ala161Ser)
c.-9G>T (n.-9G>T)
c.229G>T (p.Ala77Ser)
13g.46892522C>GCA388153063HTR2Ac.481G>C (p.Ala161Pro)
c.-9G>C (n.-9G>C)
c.229G>C (p.Ala77Pro)
13g.46892522C>TCA388153065HTR2Ac.481G>A (p.Ala161Thr)
c.-9G>A (n.-9G>A)
c.229G>A (p.Ala77Thr)
13g.46892523C>ACA483555017HTR2Ac.480G>T (p.Thr160=)
c.-10G>T (n.-10G>T)
c.228G>T (p.Thr76=)
13g.46892523C=CA2089308791HTR2Ac.480G= (p.Thr160=)
c.-10G= (n.-10G=)
c.228G= (p.Thr76=)
13g.46892523C>GCA483555018HTR2Ac.480G>C (p.Thr160=)
c.-10G>C (n.-10G>C)
c.228G>C (p.Thr76=)
13g.46892523C>TCA6977646HTR2Ac.480G>A (p.Thr160=)
c.-10G>A (n.-10G>A)
c.228G>A (p.Thr76=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.46892524G>ACA388153069HTR2Ac.479C>T (p.Thr160Met)
c.-11C>T (n.-11C>T)
c.227C>T (p.Thr76Met)
 dbSNP gnomAD v4 COSMIC COSMIC
13g.46892524G>CCA388153071HTR2Ac.479C>G (p.Thr160Arg)
c.-11C>G (n.-11C>G)
c.227C>G (p.Thr76Arg)
13g.46892524G>TCA388153073HTR2Ac.479C>A (p.Thr160Lys)
c.-11C>A (n.-11C>A)
c.227C>A (p.Thr76Lys)
13g.46892525T>ACA388153074HTR2Ac.478A>T (p.Thr160Ser)
c.-12A>T (n.-12A>T)
c.226A>T (p.Thr76Ser)
13g.46892525T>CCA388153075HTR2Ac.478A>G (p.Thr160Ala)
c.-12A>G (n.-12A>G)
c.226A>G (p.Thr76Ala)
13g.46892525T>GCA388153076HTR2Ac.478A>C (p.Thr160Pro)
c.-12A>C (n.-12A>C)
c.226A>C (p.Thr76Pro)
13g.46892526G>ACA6977647HTR2Ac.477C>T (p.Ser159=)
c.-13C>T (n.-13C>T)
c.225C>T (p.Ser75=)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.46892526G>CCA483555020HTR2Ac.477C>G (p.Ser159=)
c.-13C>G (n.-13C>G)
c.225C>G (p.Ser75=)
13g.46892526G=CA2089308795HTR2Ac.477C= (p.Ser159=)
c.-13C= (n.-13C=)
c.225C= (p.Ser75=)
13g.46892526G>TCA483555019HTR2Ac.477C>A (p.Ser159=)
c.-13C>A (n.-13C>A)
c.225C>A (p.Ser75=)
13g.46892527G>ACA388153078HTR2Ac.476C>T (p.Ser159Phe)
c.-14C>T (n.-14C>T)
c.224C>T (p.Ser75Phe)
13g.46892527G>CCA388153079HTR2Ac.476C>G (p.Ser159Cys)
c.-14C>G (n.-14C>G)
c.224C>G (p.Ser75Cys)
13g.46892527G>TCA388153080HTR2Ac.476C>A (p.Ser159Tyr)
c.-14C>A (n.-14C>A)
c.224C>A (p.Ser75Tyr)
13g.46892528A>CCA388153082HTR2Ac.475T>G (p.Ser159Ala)
c.-15T>G (n.-15T>G)
c.223T>G (p.Ser75Ala)
13g.46892528A>GCA388153084HTR2Ac.475T>C (p.Ser159Pro)
c.-15T>C (n.-15T>C)
c.223T>C (p.Ser75Pro)
13g.46892528A>TCA388153086HTR2Ac.475T>A (p.Ser159Thr)
c.-15T>A (n.-15T>A)
c.223T>A (p.Ser75Thr)
13g.46892529G>ACA483555021HTR2Ac.474C>T (p.Phe158=)
c.-16C>T (n.-16C>T)
c.222C>T (p.Phe74=)
13g.46892529G>CCA388153088HTR2Ac.474C>G (p.Phe158Leu)
c.-16C>G (n.-16C>G)
c.222C>G (p.Phe74Leu)
13g.46892529G>TCA388153089HTR2Ac.474C>A (p.Phe158Leu)
c.-16C>A (n.-16C>A)
c.222C>A (p.Phe74Leu)
13g.46892530A>CCA388153090HTR2Ac.473T>G (p.Phe158Cys)
c.-17T>G (n.-17T>G)
c.221T>G (p.Phe74Cys)
13g.46892530A>GCA388153092HTR2Ac.473T>C (p.Phe158Ser)
c.-17T>C (n.-17T>C)
c.221T>C (p.Phe74Ser)
13g.46892530A>TCA388153093HTR2Ac.473T>A (p.Phe158Tyr)
c.-17T>A (n.-17T>A)
c.221T>A (p.Phe74Tyr)
13g.46892531A=CA2089308797HTR2Ac.472T= (p.Phe158=)
c.-18T= (n.-18T=)
c.220T= (p.Phe74=)
13g.46892531A>CCA388153095HTR2Ac.472T>G (p.Phe158Val)
c.-18T>G (n.-18T>G)
c.220T>G (p.Phe74Val)
13g.46892531A>GCA249259708HTR2Ac.472T>C (p.Phe158Leu)
c.-18T>C (n.-18T>C)
c.220T>C (p.Phe74Leu)
 dbSNP
13g.46892531A>TCA388153098HTR2Ac.472T>A (p.Phe158Ile)
c.-18T>A (n.-18T>A)
c.220T>A (p.Phe74Ile)
13g.46892532G>ACA483555022HTR2Ac.471C>T (p.Leu157=)
c.-19C>T (n.-19C>T)
c.219C>T (p.Leu73=)
 dbSNP
13g.46892532G>CCA249259722HTR2Ac.471C>G (p.Leu157=)
c.-19C>G (n.-19C>G)
c.219C>G (p.Leu73=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.46892532G=CA2089308801HTR2Ac.471C= (p.Leu157=)
c.-19C= (n.-19C=)
c.219C= (p.Leu73=)
13g.46892532G>TCA483555023HTR2Ac.471C>A (p.Leu157=)
c.-19C>A (n.-19C>A)
c.219C>A (p.Leu73=)
13g.46892533A>CCA388153100HTR2Ac.470T>G (p.Leu157Arg)
c.-20T>G (n.-20T>G)
c.218T>G (p.Leu73Arg)
13g.46892533A>GCA388153103HTR2Ac.470T>C (p.Leu157Pro)
c.-20T>C (n.-20T>C)
c.218T>C (p.Leu73Pro)
13g.46892533A>TCA388153105HTR2Ac.470T>A (p.Leu157His)
c.-20T>A (n.-20T>A)
c.218T>A (p.Leu73His)
13g.46892534G>ACA388153107HTR2Ac.469C>T (p.Leu157Phe)
c.-21C>T (n.-21C>T)
c.217C>T (p.Leu73Phe)
 dbSNP gnomAD v4
13g.46892534G>CCA388153108HTR2Ac.469C>G (p.Leu157Val)
c.-21C>G (n.-21C>G)
c.217C>G (p.Leu73Val)
13g.46892534G=CA2089308807HTR2Ac.469C= (p.Leu157=)
c.-21C= (n.-21C=)
c.217C= (p.Leu73=)
13g.46892534G>TCA388153110HTR2Ac.469C>A (p.Leu157Ile)
c.-21C>A (n.-21C>A)
c.217C>A (p.Leu73Ile)
13g.46892535C>ACA483555025HTR2Ac.468G>T (p.Val156=)
c.-22G>T (n.-22G>T)
c.216G>T (p.Val72=)
13g.46892535C>GCA483555026HTR2Ac.468G>C (p.Val156=)
c.-22G>C (n.-22G>C)
c.216G>C (p.Val72=)
13g.46892535C>TCA483555024HTR2Ac.468G>A (p.Val156=)
c.-22G>A (n.-22G>A)
c.216G>A (p.Val72=)
13g.46892536A>CCA388153114HTR2Ac.467T>G (p.Val156Gly)
c.-23T>G (n.-23T>G)
c.215T>G (p.Val72Gly)
13g.46892536A>GCA388153116HTR2Ac.467T>C (p.Val156Ala)
c.-23T>C (n.-23T>C)
c.215T>C (p.Val72Ala)
13g.46892536A>TCA388153112HTR2Ac.467T>A (p.Val156Glu)
c.-23T>A (n.-23T>A)
c.215T>A (p.Val72Glu)
13g.46892537C>ACA388153118HTR2Ac.466G>T (p.Val156Leu)
c.-24G>T (n.-24G>T)
c.214G>T (p.Val72Leu)
 dbSNP
13g.46892537C=CA2089308810HTR2Ac.466G= (p.Val156=)
c.-24G= (n.-24G=)
c.214G= (p.Val72=)
13g.46892537C>GCA388153121HTR2Ac.466G>C (p.Val156Leu)
c.-24G>C (n.-24G>C)
c.214G>C (p.Val72Leu)
13g.46892537C>TCA388153122HTR2Ac.466G>A (p.Val156Met)
c.-24G>A (n.-24G>A)
c.214G>A (p.Val72Met)
 dbSNP gnomAD v4
13g.46892538G>ACA483555027HTR2Ac.465C>T (p.Asp155=)
c.-25C>T (n.-25C>T)
c.213C>T (p.Asp71=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.46892538G>CCA6977648HTR2Ac.465C>G (p.Asp155Glu)
c.-25C>G (n.-25C>G)
c.213C>G (p.Asp71Glu)
 dbSNP ExAC gnomAD v2
13g.46892538G=CA2089308812HTR2Ac.465C= (p.Asp155=)
c.-25C= (n.-25C=)
c.213C= (p.Asp71=)
13g.46892538G>TCA388153126HTR2Ac.465C>A (p.Asp155Glu)
c.-25C>A (n.-25C>A)
c.213C>A (p.Asp71Glu)
13g.46892539T>ACA388153133HTR2Ac.464A>T (p.Asp155Val)
c.-26A>T (n.-26A>T)
c.212A>T (p.Asp71Val)
13g.46892539T>CCA388153129HTR2Ac.464A>G (p.Asp155Gly)
c.-26A>G (n.-26A>G)
c.212A>G (p.Asp71Gly)
13g.46892539T>GCA388153131HTR2Ac.464A>C (p.Asp155Ala)
c.-26A>C (n.-26A>C)
c.212A>C (p.Asp71Ala)
13g.46892540C>ACA388153135HTR2Ac.463G>T (p.Asp155Tyr)
c.-27G>T (n.-27G>T)
c.211G>T (p.Asp71Tyr)
13g.46892540C>GCA388153136HTR2Ac.463G>C (p.Asp155His)
c.-27G>C (n.-27G>C)
c.211G>C (p.Asp71His)
13g.46892540C>TCA388153139HTR2Ac.463G>A (p.Asp155Asn)
c.-27G>A (n.-27G>A)
c.211G>A (p.Asp71Asn)
13g.46892541C>ACA483555028HTR2Ac.462G>T (p.Leu154=)
c.-28G>T (n.-28G>T)
c.210G>T (p.Leu70=)
13g.46892541C=CA2089308816HTR2Ac.462G= (p.Leu154=)
c.-28G= (n.-28G=)
c.210G= (p.Leu70=)
13g.46892541C>GCA483555029HTR2Ac.462G>C (p.Leu154=)
c.-28G>C (n.-28G>C)
c.210G>C (p.Leu70=)
13g.46892541C>TCA483555030HTR2Ac.462G>A (p.Leu154=)
c.-28G>A (n.-28G>A)
c.210G>A (p.Leu70=)
 dbSNP
13g.46892542A>CCA388153141HTR2Ac.461T>G (p.Leu154Arg)
c.-29T>G (n.-29T>G)
c.209T>G (p.Leu70Arg)
13g.46892542A>GCA388153143HTR2Ac.461T>C (p.Leu154Pro)
c.-29T>C (n.-29T>C)
c.209T>C (p.Leu70Pro)
13g.46892542A>TCA388153145HTR2Ac.461T>A (p.Leu154Gln)
c.-29T>A (n.-29T>A)
c.209T>A (p.Leu70Gln)
13g.46892543G>ACA483555031HTR2Ac.460C>T (p.Leu154=)
c.-30C>T (n.-30C>T)
c.208C>T (p.Leu70=)
13g.46892543G>CCA388153147HTR2Ac.460C>G (p.Leu154Val)
c.-30C>G (n.-30C>G)
c.208C>G (p.Leu70Val)
13g.46892543G>TCA388153149HTR2Ac.460C>A (p.Leu154Met)
c.-30C>A (n.-30C>A)
c.208C>A (p.Leu70Met)
13g.46892544G>ACA483555032HTR2Ac.459C>T (p.Tyr153=)
c.-31C>T (n.-31C>T)
c.207C>T (p.Tyr69=)
13g.46892544G>CCA388153152HTR2Ac.459C>G (p.Tyr153Ter)
c.-31C>G (n.-31C>G)
c.207C>G (p.Tyr69Ter)
 dbSNP gnomAD v3 gnomAD v4
13g.46892544G=CA2089308817HTR2Ac.459C= (p.Tyr153=)
c.-31C= (n.-31C=)
c.207C= (p.Tyr69=)
13g.46892544G>TCA388153153HTR2Ac.459C>A (p.Tyr153Ter)
c.-31C>A (n.-31C>A)
c.207C>A (p.Tyr69Ter)
13g.46892545T>ACA388153156HTR2Ac.458A>T (p.Tyr153Phe)
c.-32A>T (n.-32A>T)
c.206A>T (p.Tyr69Phe)
13g.46892545T>CCA388153158HTR2Ac.458A>G (p.Tyr153Cys)
c.-32A>G (n.-32A>G)
c.206A>G (p.Tyr69Cys)
13g.46892545T>GCA388153161HTR2Ac.458A>C (p.Tyr153Ser)
c.-32A>C (n.-32A>C)
c.206A>C (p.Tyr69Ser)
13g.46892546A>CCA388153163HTR2Ac.457T>G (p.Tyr153Asp)
c.-33T>G (n.-33T>G)
c.205T>G (p.Tyr69Asp)
13g.46892546A>GCA388153165HTR2Ac.457T>C (p.Tyr153His)
c.-33T>C (n.-33T>C)
c.205T>C (p.Tyr69His)
13g.46892546A>TCA388153167HTR2Ac.457T>A (p.Tyr153Asn)
c.-33T>A (n.-33T>A)
c.205T>A (p.Tyr69Asn)
13g.46892547A>CCA388153169HTR2Ac.456T>G (p.Ile152Met)
c.-34T>G (n.-34T>G)
c.204T>G (p.Ile68Met)
13g.46892547A>GCA483555033HTR2Ac.456T>C (p.Ile152=)
c.-34T>C (n.-34T>C)
c.204T>C (p.Ile68=)
13g.46892547A>TCA483555034HTR2Ac.456T>A (p.Ile152=)
c.-34T>A (n.-34T>A)
c.204T>A (p.Ile68=)
13g.46892548A>CCA388153170HTR2Ac.455T>G (p.Ile152Ser)
c.-35T>G (n.-35T>G)
c.203T>G (p.Ile68Ser)
13g.46892548A>GCA388153172HTR2Ac.455T>C (p.Ile152Thr)
c.-35T>C (n.-35T>C)
c.203T>C (p.Ile68Thr)
13g.46892548A>TCA388153174HTR2Ac.455T>A (p.Ile152Asn)
c.-35T>A (n.-35T>A)
c.203T>A (p.Ile68Asn)
13g.46892549T>ACA388153177HTR2Ac.454A>T (p.Ile152Phe)
c.-36A>T (n.-36A>T)
c.202A>T (p.Ile68Phe)
13g.46892549T>CCA388153179HTR2Ac.454A>G (p.Ile152Val)
c.-36A>G (n.-36A>G)
c.202A>G (p.Ile68Val)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.46892549T>GCA388153181HTR2Ac.454A>C (p.Ile152Leu)
c.-36A>C (n.-36A>C)
c.202A>C (p.Ile68Leu)
 dbSNP gnomAD v3 gnomAD v4
13g.46892549T=CA2089308819HTR2Ac.454A= (p.Ile152=)
c.-36A= (n.-36A=)
c.202A= (p.Ile68=)
13g.46892550C>ACA388153184HTR2Ac.453G>T (p.Trp151Cys)
c.-37G>T (n.-37G>T)
c.201G>T (p.Trp67Cys)
13g.46892550C>GCA388153188HTR2Ac.453G>C (p.Trp151Cys)
c.-37G>C (n.-37G>C)
c.201G>C (p.Trp67Cys)
13g.46892550C>TCA388153186HTR2Ac.453G>A (p.Trp151Ter)
c.-37G>A (n.-37G>A)
c.201G>A (p.Trp67Ter)
 COSMIC
13g.46892551C>ACA388153190HTR2Ac.452G>T (p.Trp151Leu)
c.-38G>T (n.-38G>T)
c.200G>T (p.Trp67Leu)
13g.46892551C>GCA388153192HTR2Ac.452G>C (p.Trp151Ser)
c.-38G>C (n.-38G>C)
c.200G>C (p.Trp67Ser)
13g.46892551C>TCA388153194HTR2Ac.452G>A (p.Trp151Ter)
c.-38G>A (n.-38G>A)
c.200G>A (p.Trp67Ter)
13g.46892552A=CA2089308822HTR2Ac.451T= (p.Trp151=)
c.-39T= (n.-39T=)
c.199T= (p.Trp67=)
13g.46892552A>CCA388153196HTR2Ac.451T>G (p.Trp151Gly)
c.-39T>G (n.-39T>G)
c.199T>G (p.Trp67Gly)
13g.46892552A>GCA388153198HTR2Ac.451T>C (p.Trp151Arg)
c.-39T>C (n.-39T>C)
c.199T>C (p.Trp67Arg)
 dbSNP gnomAD v4
13g.46892552A>TCA388153199HTR2Ac.451T>A (p.Trp151Arg)
c.-39T>A (n.-39T>A)
c.199T>A (p.Trp67Arg)
13g.46892553G>ACA483555035HTR2Ac.450C>T (p.Val150=)
c.-40C>T (n.-40C>T)
c.198C>T (p.Val66=)
13g.46892553G>CCA483555036HTR2Ac.450C>G (p.Val150=)
c.-40C>G (n.-40C>G)
c.198C>G (p.Val66=)
13g.46892553G>TCA483555037HTR2Ac.450C>A (p.Val150=)
c.-40C>A (n.-40C>A)
c.198C>A (p.Val66=)
13g.46892554A=CA2089308824HTR2Ac.449T= (p.Val150=)
c.-41T= (n.-41T=)
c.197T= (p.Val66=)
13g.46892554A>CCA388153203HTR2Ac.449T>G (p.Val150Gly)
c.-41T>G (n.-41T>G)
c.197T>G (p.Val66Gly)
13g.46892554A>GCA388153204HTR2Ac.449T>C (p.Val150Ala)
c.-41T>C (n.-41T>C)
c.197T>C (p.Val66Ala)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.46892554A>TCA388153205HTR2Ac.449T>A (p.Val150Asp)
c.-41T>A (n.-41T>A)
c.197T>A (p.Val66Asp)
13g.46892555C>ACA388153207HTR2Ac.448G>T (p.Val150Phe)
c.-42G>T (n.-42G>T)
c.196G>T (p.Val66Phe)
13g.46892555C>GCA388153209HTR2Ac.448G>C (p.Val150Leu)
c.-42G>C (n.-42G>C)
c.196G>C (p.Val66Leu)
 gnomAD v4
13g.46892555C>TCA388153211HTR2Ac.448G>A (p.Val150Ile)
c.-42G>A (n.-42G>A)
c.196G>A (p.Val66Ile)
 gnomAD v4
13g.46892556T>ACA483555038HTR2Ac.447A>T (p.Ala149=)
c.-43A>T (n.-43A>T)
c.195A>T (p.Ala65=)
13g.46892556T>CCA483555040HTR2Ac.447A>G (p.Ala149=)
c.-43A>G (n.-43A>G)
c.195A>G (p.Ala65=)
 dbSNP
13g.46892556T>GCA483555039HTR2Ac.447A>C (p.Ala149=)
c.-43A>C (n.-43A>C)
c.195A>C (p.Ala65=)
13g.46892556T=CA2089308826HTR2Ac.447A= (p.Ala149=)
c.-43A= (n.-43A=)
c.195A= (p.Ala65=)
13g.46892557G>ACA388153213HTR2Ac.446C>T (p.Ala149Val)
c.-44C>T (n.-44C>T)
c.194C>T (p.Ala65Val)
13g.46892557G>CCA388153217HTR2Ac.446C>G (p.Ala149Gly)
c.-44C>G (n.-44C>G)
c.194C>G (p.Ala65Gly)
13g.46892557G>TCA388153215HTR2Ac.446C>A (p.Ala149Glu)
c.-44C>A (n.-44C>A)
c.194C>A (p.Ala65Glu)
 COSMIC
13g.46892558C>ACA388153219HTR2Ac.445G>T (p.Ala149Ser)
c.-45G>T (n.-45G>T)
c.193G>T (p.Ala65Ser)
13g.46892558C>GCA388153221HTR2Ac.445G>C (p.Ala149Pro)
c.-45G>C (n.-45G>C)
c.193G>C (p.Ala65Pro)
13g.46892558C>TCA388153223HTR2Ac.445G>A (p.Ala149Thr)
c.-45G>A (n.-45G>A)
c.193G>A (p.Ala65Thr)
13g.46892559A>CCA388153224HTR2Ac.444T>G (p.Cys148Trp)
c.-46T>G (n.-46T>G)
c.192T>G (p.Cys64Trp)
13g.46892559A>GCA483555042HTR2Ac.444T>C (p.Cys148=)
c.-46T>C (n.-46T>C)
c.192T>C (p.Cys64=)
 dbSNP
13g.46892559A>TCA388153226HTR2Ac.444T>A (p.Cys148Ter)
c.-46T>A (n.-46T>A)
c.192T>A (p.Cys64Ter)
13g.46892560C>ACA388153234HTR2Ac.443G>T (p.Cys148Phe)
c.-47G>T (n.-47G>T)
c.191G>T (p.Cys64Phe)
13g.46892560C>GCA388153232HTR2Ac.443G>C (p.Cys148Ser)
c.-47G>C (n.-47G>C)
c.191G>C (p.Cys64Ser)
 gnomAD v4
13g.46892560C>TCA388153229HTR2Ac.443G>A (p.Cys148Tyr)
c.-47G>A (n.-47G>A)
c.191G>A (p.Cys64Tyr)
13g.46892561A>CCA388153237HTR2Ac.442T>G (p.Cys148Gly)
c.-48T>G (n.-48T>G)
c.190T>G (p.Cys64Gly)
13g.46892561A>GCA388153238HTR2Ac.442T>C (p.Cys148Arg)
c.-48T>C (n.-48T>C)
c.190T>C (p.Cys64Arg)
13g.46892561A>TCA388153240HTR2Ac.442T>A (p.Cys148Ser)
c.-48T>A (n.-48T>A)
c.190T>A (p.Cys64Ser)
13g.46892562A>CCA483555043HTR2Ac.441T>G (p.Leu147=)
c.-49T>G (n.-49T>G)
c.189T>G (p.Leu63=)
13g.46892562A>GCA483555044HTR2Ac.441T>C (p.Leu147=)
c.-49T>C (n.-49T>C)
c.189T>C (p.Leu63=)
 COSMIC
13g.46892562A>TCA483555045HTR2Ac.441T>A (p.Leu147=)
c.-49T>A (n.-49T>A)
c.189T>A (p.Leu63=)
13g.46892563A>CCA388153243HTR2Ac.440T>G (p.Leu147Arg)
c.-50T>G (n.-50T>G)
c.188T>G (p.Leu63Arg)
13g.46892563A>GCA388153245HTR2Ac.440T>C (p.Leu147Pro)
c.-50T>C (n.-50T>C)
c.188T>C (p.Leu63Pro)
13g.46892563A>TCA388153247HTR2Ac.440T>A (p.Leu147His)
c.-50T>A (n.-50T>A)
c.188T>A (p.Leu63His)
13g.46892564G>ACA388153249HTR2Ac.439C>T (p.Leu147Phe)
c.-51C>T (n.-51C>T)
c.187C>T (p.Leu63Phe)
 gnomAD v4
13g.46892564G>CCA388153252HTR2Ac.439C>G (p.Leu147Val)
c.-51C>G (n.-51C>G)
c.187C>G (p.Leu63Val)
13g.46892564G>TCA388153251HTR2Ac.439C>A (p.Leu147Ile)
c.-51C>A (n.-51C>A)
c.187C>A (p.Leu63Ile)
13g.46892565C>ACA388153254HTR2Ac.438G>T (p.Lys146Asn)
c.-52G>T (n.-52G>T)
c.186G>T (p.Lys62Asn)
13g.46892565C>GCA388153256HTR2Ac.438G>C (p.Lys146Asn)
c.-52G>C (n.-52G>C)
c.186G>C (p.Lys62Asn)
13g.46892565C>TCA483555047HTR2Ac.438G>A (p.Lys146=)
c.-52G>A (n.-52G>A)
c.186G>A (p.Lys62=)
13g.46892566T>ACA388153258HTR2Ac.437A>T (p.Lys146Met)
c.-53A>T (n.-53A>T)
c.185A>T (p.Lys62Met)
13g.46892566T>CCA388153260HTR2Ac.437A>G (p.Lys146Arg)
c.-53A>G (n.-53A>G)
c.185A>G (p.Lys62Arg)
13g.46892566T>GCA388153262HTR2Ac.437A>C (p.Lys146Thr)
c.-53A>C (n.-53A>C)
c.185A>C (p.Lys62Thr)
 gnomAD v4
13g.46892567T>ACA388153264HTR2Ac.436A>T (p.Lys146Ter)
c.-54A>T (n.-54A>T)
c.184A>T (p.Lys62Ter)
13g.46892567T>CCA388153266HTR2Ac.436A>G (p.Lys146Glu)
c.-54A>G (n.-54A>G)
c.184A>G (p.Lys62Glu)
13g.46892567T>GCA388153269HTR2Ac.436A>C (p.Lys146Gln)
c.-54A>C (n.-54A>C)
c.184A>C (p.Lys62Gln)
 dbSNP gnomAD v2 gnomAD v4
13g.46892567T=CA2089308833HTR2Ac.436A= (p.Lys146=)
c.-54A= (n.-54A=)
c.184A= (p.Lys62=)
13g.46892568G>ACA483555048HTR2Ac.435C>T (p.Ser145=)
c.-55C>T (n.-55C>T)
c.183C>T (p.Ser61=)
13g.46892568G>CCA388153271HTR2Ac.435C>G (p.Ser145Arg)
c.-55C>G (n.-55C>G)
c.183C>G (p.Ser61Arg)
13g.46892568G>TCA388153273HTR2Ac.435C>A (p.Ser145Arg)
c.-55C>A (n.-55C>A)
c.183C>A (p.Ser61Arg)
13g.46892569C>ACA388153276HTR2Ac.434G>T (p.Ser145Ile)
c.-56G>T (n.-56G>T)
c.182G>T (p.Ser61Ile)
13g.46892569C>GCA388153280HTR2Ac.434G>C (p.Ser145Thr)
c.-56G>C (n.-56G>C)
c.182G>C (p.Ser61Thr)
13g.46892569C>TCA388153278HTR2Ac.434G>A (p.Ser145Asn)
c.-56G>A (n.-56G>A)
c.182G>A (p.Ser61Asn)
13g.46892570T>ACA388153283HTR2Ac.433A>T (p.Ser145Cys)
c.-57A>T (n.-57A>T)
c.181A>T (p.Ser61Cys)
13g.46892570T>CCA388153286HTR2Ac.433A>G (p.Ser145Gly)
c.-57A>G (n.-57A>G)
c.181A>G (p.Ser61Gly)
13g.46892570T>GCA388153285HTR2Ac.433A>C (p.Ser145Arg)
c.-57A>C (n.-57A>C)
c.181A>C (p.Ser61Arg)
13g.46892571C>ACA483555050HTR2Ac.432G>T (p.Pro144=)
c.-58G>T (n.-58G>T)
c.180G>T (p.Pro60=)
13g.46892571C=CA2089308836HTR2Ac.432G= (p.Pro144=)
c.-58G= (n.-58G=)
c.180G= (p.Pro60=)
13g.46892571C>GCA6977649HTR2Ac.432G>C (p.Pro144=)
c.-58G>C (n.-58G>C)
c.180G>C (p.Pro60=)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.46892571C>TCA6977650HTR2Ac.432G>A (p.Pro144=)
c.-58G>A (n.-58G>A)
c.180G>A (p.Pro60=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.46892572G>ACA388153290HTR2Ac.431C>T (p.Pro144Leu)
c.-59C>T (n.-59C>T)
c.179C>T (p.Pro60Leu)
 dbSNP gnomAD v3 gnomAD v4 COSMIC
13g.46892572G>CCA388153292HTR2Ac.431C>G (p.Pro144Arg)
c.-59C>G (n.-59C>G)
c.179C>G (p.Pro60Arg)
13g.46892572G>TCA388153294HTR2Ac.431C>A (p.Pro144Gln)
c.-59C>A (n.-59C>A)
c.179C>A (p.Pro60Gln)
 gnomAD v4
13g.46892573G>ACA388153296HTR2Ac.430C>T (p.Pro144Ser)
c.-60C>T (n.-60C>T)
c.178C>T (p.Pro60Ser)
 COSMIC COSMIC
13g.46892573G>CCA388153298HTR2Ac.430C>G (p.Pro144Ala)
c.-60C>G (n.-60C>G)
c.178C>G (p.Pro60Ala)
13g.46892573G>TCA388153299HTR2Ac.430C>A (p.Pro144Thr)
c.-60C>A (n.-60C>A)
c.178C>A (p.Pro60Thr)
 gnomAD v4
13g.46892574C>ACA483555051HTR2Ac.429G>T (p.Leu143=)
c.-61G>T (n.-61G>T)
c.177G>T (p.Leu59=)
13g.46892574C>GCA483555052HTR2Ac.429G>C (p.Leu143=)
c.-61G>C (n.-61G>C)
c.177G>C (p.Leu59=)
13g.46892574C>TCA483555053HTR2Ac.429G>A (p.Leu143=)
c.-61G>A (n.-61G>A)
c.177G>A (p.Leu59=)
13g.46892575A>CCA388153303HTR2Ac.428T>G (p.Leu143Arg)
c.-62T>G (n.-62T>G)
c.176T>G (p.Leu59Arg)
13g.46892575A>GCA388153305HTR2Ac.428T>C (p.Leu143Pro)
c.-62T>C (n.-62T>C)
c.176T>C (p.Leu59Pro)
13g.46892575A>TCA388153307HTR2Ac.428T>A (p.Leu143Gln)
c.-62T>A (n.-62T>A)
c.176T>A (p.Leu59Gln)
13g.46892576G>ACA483555054HTR2Ac.427C>T (p.Leu143=)
c.-63C>T (n.-63C>T)
c.175C>T (p.Leu59=)
13g.46892576G>CCA388153309HTR2Ac.427C>G (p.Leu143Val)
c.-63C>G (n.-63C>G)
c.175C>G (p.Leu59Val)
13g.46892576G>TCA388153311HTR2Ac.427C>A (p.Leu143Met)
c.-63C>A (n.-63C>A)
c.175C>A (p.Leu59Met)
13g.46892577A=CA2089308837HTR2Ac.426T= (p.Pro142=)
c.-64T= (n.-64T=)
c.174T= (p.Pro58=)
13g.46892577A>CCA483555057HTR2Ac.426T>G (p.Pro142=)
c.-64T>G (n.-64T>G)
c.174T>G (p.Pro58=)
13g.46892577A>GCA483555056HTR2Ac.426T>C (p.Pro142=)
c.-64T>C (n.-64T>C)
c.174T>C (p.Pro58=)
13g.46892577A>TCA483555055HTR2Ac.426T>A (p.Pro142=)
c.-64T>A (n.-64T>A)
c.174T>A (p.Pro58=)
13g.46892577_46892578insACTAAGGCATTTCTGAAAATCATTCA919264937HTR2Ac.425_426insAATGATTTTCAGAAATGCCTTAGT (p.Pro142_Leu143insMetIlePheArgAsnAlaLeuVal)
c.-65_-64insAATGATTTTCAGAAATGCCTTAGT (n.-65_-64insAATGATTTTCAGAAATGCCTTAGT)
c.173_174insAATGATTTTCAGAAATGCCTTAGT (p.Pro58_Leu59insMetIlePheArgAsnAlaLeuVal)
 dbSNP
13g.46892578G>ACA388153316HTR2Ac.425C>T (p.Pro142Leu)
c.-65C>T (n.-65C>T)
c.173C>T (p.Pro58Leu)
13g.46892578G>CCA388153315HTR2Ac.425C>G (p.Pro142Arg)
c.-65C>G (n.-65C>G)
c.173C>G (p.Pro58Arg)
13g.46892578G>TCA388153314HTR2Ac.425C>A (p.Pro142His)
c.-65C>A (n.-65C>A)
c.173C>A (p.Pro58His)
13g.46892579G>ACA388153320HTR2Ac.424C>T (p.Pro142Ser)
c.-66C>T (n.-66C>T)
c.172C>T (p.Pro58Ser)
13g.46892579G>CCA388153322HTR2Ac.424C>G (p.Pro142Ala)
c.-66C>G (n.-66C>G)
c.172C>G (p.Pro58Ala)
13g.46892579G>TCA388153324HTR2Ac.424C>A (p.Pro142Thr)
c.-66C>A (n.-66C>A)
c.172C>A (p.Pro58Thr)
13g.46892580C>ACA388153326HTR2Ac.423G>T (p.Trp141Cys)
c.-67G>T (n.-67G>T)
c.171G>T (p.Trp57Cys)
 COSMIC
13g.46892580C=CA2089308841HTR2Ac.423G= (p.Trp141=)
c.-67G= (n.-67G=)
c.171G= (p.Trp57=)
13g.46892580C>GCA388153329HTR2Ac.423G>C (p.Trp141Cys)
c.-67G>C (n.-67G>C)
c.171G>C (p.Trp57Cys)
13g.46892580C>TCA388153331HTR2Ac.423G>A (p.Trp141Ter)
c.-67G>A (n.-67G>A)
c.171G>A (p.Trp57Ter)
 dbSNP
13g.46892581C>ACA388153333HTR2Ac.422G>T (p.Trp141Leu)
c.-68G>T (n.-68G>T)
c.170G>T (p.Trp57Leu)
13g.46892581C>GCA388153335HTR2Ac.422G>C (p.Trp141Ser)
c.-68G>C (n.-68G>C)
c.170G>C (p.Trp57Ser)
13g.46892581C>TCA388153337HTR2Ac.422G>A (p.Trp141Ter)
c.-68G>A (n.-68G>A)
c.170G>A (p.Trp57Ter)
13g.46892582A=CA2089308843HTR2Ac.421T= (p.Trp141=)
c.-69T= (n.-69T=)
c.169T= (p.Trp57=)
13g.46892582A>CCA388153339HTR2Ac.421T>G (p.Trp141Gly)
c.-69T>G (n.-69T>G)
c.169T>G (p.Trp57Gly)
13g.46892582A>GCA388153341HTR2Ac.421T>C (p.Trp141Arg)
c.-69T>C (n.-69T>C)
c.169T>C (p.Trp57Arg)
 dbSNP gnomAD v2 gnomAD v4
13g.46892582A>TCA388153343HTR2Ac.421T>A (p.Trp141Arg)
c.-69T>A (n.-69T>A)
c.169T>A (p.Trp57Arg)
 gnomAD v4
13g.46892583C>ACA483555064HTR2Ac.420G>T (p.Arg140=)
c.-70G>T (n.-70G>T)
c.168G>T (p.Arg56=)
13g.46892583C>GCA483555066HTR2Ac.420G>C (p.Arg140=)
c.-70G>C (n.-70G>C)
c.168G>C (p.Arg56=)
13g.46892583C>TCA483555065HTR2Ac.420G>A (p.Arg140=)
c.-70G>A (n.-70G>A)
c.168G>A (p.Arg56=)

Number of alleles fetched