Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.23375166T>ACA387554493SACSn.697A>T
c.161A>T (p.Asp54Val)
c.124A>T (p.Thr42Ser)
n.262A>T
c.115A>T (p.Thr39Ser)
n.241A>T
c.-2039A>T (n.-2039A>T)
c.-230A>T (n.-230A>T)
c.148A>T (p.Thr50Ser)
13g.23375166T>CCA387554484SACSn.697A>G
c.161A>G (p.Asp54Gly)
c.124A>G (p.Thr42Ala)
n.262A>G
c.115A>G (p.Thr39Ala)
n.241A>G
c.-2039A>G (n.-2039A>G)
c.-230A>G (n.-230A>G)
c.148A>G (p.Thr50Ala)
ClinVar dbSNP gnomAD v2 gnomAD v4
13g.23375166T>GCA387554485SACSn.697A>C
c.161A>C (p.Asp54Ala)
c.124A>C (p.Thr42Pro)
n.262A>C
c.115A>C (p.Thr39Pro)
n.241A>C
c.-2039A>C (n.-2039A>C)
c.-230A>C (n.-230A>C)
c.148A>C (p.Thr50Pro)
gnomAD v4
13g.23375166T=CA2078656725SACSn.697A=
c.161A= (p.Asp54=)
c.124A= (p.Thr42=)
n.262A=
c.115A= (p.Thr39=)
n.241A=
c.-2039A= (n.-2039A=)
c.-230A= (n.-230A=)
c.148A= (p.Thr50=)
13g.23375167C>ACA387554496SACSn.696G>T
c.160G>T (p.Asp54Tyr)
c.123G>T (p.Glu41Asp)
n.261G>T
c.114G>T (p.Glu38Asp)
n.240G>T
c.-2040G>T (n.-2040G>T)
c.-231G>T (n.-231G>T)
c.147G>T (p.Glu49Asp)
gnomAD v4
13g.23375167C>GCA387554498SACSn.696G>C
c.160G>C (p.Asp54His)
c.123G>C (p.Glu41Asp)
n.261G>C
c.114G>C (p.Glu38Asp)
n.240G>C
c.-2040G>C (n.-2040G>C)
c.-231G>C (n.-231G>C)
c.147G>C (p.Glu49Asp)
13g.23375167C>TCA482928831SACSn.696G>A
c.160G>A (p.Asp54Asn)
c.123G>A (p.Glu41=)
n.261G>A
c.114G>A (p.Glu38=)
n.240G>A
c.-2040G>A (n.-2040G>A)
c.-231G>A (n.-231G>A)
c.147G>A (p.Glu49=)
13g.23375168T>ACA387554499SACSn.695A>T
c.159A>T (p.Gly53=)
c.122A>T (p.Glu41Val)
n.260A>T
c.113A>T (p.Glu38Val)
n.239A>T
c.-2041A>T (n.-2041A>T)
c.-232A>T (n.-232A>T)
c.146A>T (p.Glu49Val)
gnomAD v4
13g.23375168T>CCA387554500SACSn.695A>G
c.159A>G (p.Gly53=)
c.122A>G (p.Glu41Gly)
n.260A>G
c.113A>G (p.Glu38Gly)
n.239A>G
c.-2041A>G (n.-2041A>G)
c.-232A>G (n.-232A>G)
c.146A>G (p.Glu49Gly)
gnomAD v4
13g.23375168T>GCA387554502SACSn.695A>C
c.159A>C (p.Gly53=)
c.122A>C (p.Glu41Ala)
n.260A>C
c.113A>C (p.Glu38Ala)
n.239A>C
c.-2041A>C (n.-2041A>C)
c.-232A>C (n.-232A>C)
c.146A>C (p.Glu49Ala)
13g.23375169C>ACA387554504SACSn.694G>T
c.158G>T (p.Gly53Val)
c.121G>T (p.Glu41Ter)
n.259G>T
c.112G>T (p.Glu38Ter)
n.238G>T
c.-2042G>T (n.-2042G>T)
c.-233G>T (n.-233G>T)
c.145G>T (p.Glu49Ter)
gnomAD v4
13g.23375169C=CA2078656727SACSn.694G=
c.158G= (p.Gly53=)
c.121G= (p.Glu41=)
n.259G=
c.112G= (p.Glu38=)
n.238G=
c.-2042G= (n.-2042G=)
c.-233G= (n.-233G=)
c.145G= (p.Glu49=)
13g.23375169C>GCA387554505SACSn.694G>C
c.158G>C (p.Gly53Ala)
c.121G>C (p.Glu41Gln)
n.259G>C
c.112G>C (p.Glu38Gln)
n.238G>C
c.-2042G>C (n.-2042G>C)
c.-233G>C (n.-233G>C)
c.145G>C (p.Glu49Gln)
dbSNP
13g.23375169C>TCA387554507SACSn.694G>A
c.158G>A (p.Gly53Glu)
c.121G>A (p.Glu41Lys)
n.259G>A
c.112G>A (p.Glu38Lys)
n.238G>A
c.-2042G>A (n.-2042G>A)
c.-233G>A (n.-233G>A)
c.145G>A (p.Glu49Lys)
13g.23375170C>ACA482928836SACSn.693G>T
c.157G>T (p.Gly53Ter)
c.120G>T (p.Ala40=)
n.258G>T
c.111G>T (p.Ala37=)
n.237G>T
c.-2043G>T (n.-2043G>T)
c.-234G>T (n.-234G>T)
c.144G>T (p.Ala48=)
gnomAD v4
13g.23375170C>GCA482928838SACSn.693G>C
c.157G>C (p.Gly53Arg)
c.120G>C (p.Ala40=)
n.258G>C
c.111G>C (p.Ala37=)
n.237G>C
c.-2043G>C (n.-2043G>C)
c.-234G>C (n.-234G>C)
c.144G>C (p.Ala48=)
ClinVar gnomAD v4
13g.23375170C>TCA482928840SACSn.693G>A
c.157G>A (p.Gly53Arg)
c.120G>A (p.Ala40=)
n.258G>A
c.111G>A (p.Ala37=)
n.237G>A
c.-2043G>A (n.-2043G>A)
c.-234G>A (n.-234G>A)
c.144G>A (p.Ala48=)
gnomAD v4
13g.23375171G>ACA387554509SACSn.692C>T
c.156C>T (p.Arg52=)
c.119C>T (p.Ala40Val)
n.257C>T
c.110C>T (p.Ala37Val)
n.236C>T
c.-2044C>T (n.-2044C>T)
c.-235C>T (n.-235C>T)
c.143C>T (p.Ala48Val)
dbSNP gnomAD v4
13g.23375171G>CCA387554510SACSn.692C>G
c.156C>G (p.Arg52=)
c.119C>G (p.Ala40Gly)
n.257C>G
c.110C>G (p.Ala37Gly)
n.236C>G
c.-2044C>G (n.-2044C>G)
c.-235C>G (n.-235C>G)
c.143C>G (p.Ala48Gly)
13g.23375171G=CA2078656728SACSn.692C=
c.156C= (p.Arg52=)
c.119C= (p.Ala40=)
n.257C=
c.110C= (p.Ala37=)
n.236C=
c.-2044C= (n.-2044C=)
c.-235C= (n.-235C=)
c.143C= (p.Ala48=)
13g.23375171G>TCA387554511SACSn.692C>A
c.156C>A (p.Arg52=)
c.119C>A (p.Ala40Glu)
n.257C>A
c.110C>A (p.Ala37Glu)
n.236C>A
c.-2044C>A (n.-2044C>A)
c.-235C>A (n.-235C>A)
c.143C>A (p.Ala48Glu)
dbSNP gnomAD v3 gnomAD v4
13g.23375172C>ACA246691821SACSn.691G>T
c.155G>T (p.Arg52Leu)
c.118G>T (p.Ala40Ser)
n.256G>T
c.109G>T (p.Ala37Ser)
n.235G>T
c.-2045G>T (n.-2045G>T)
c.-236G>T (n.-236G>T)
c.142G>T (p.Ala48Ser)
dbSNP gnomAD v4
13g.23375172C=CA2078656731SACSn.691G=
c.155G= (p.Arg52=)
c.118G= (p.Ala40=)
n.256G=
c.109G= (p.Ala37=)
n.235G=
c.-2045G= (n.-2045G=)
c.-236G= (n.-236G=)
c.142G= (p.Ala48=)
13g.23375172C>GCA387554512SACSn.691G>C
c.155G>C (p.Arg52Pro)
c.118G>C (p.Ala40Pro)
n.256G>C
c.109G>C (p.Ala37Pro)
n.235G>C
c.-2045G>C (n.-2045G>C)
c.-236G>C (n.-236G>C)
c.142G>C (p.Ala48Pro)
13g.23375172C>TCA387554514SACSn.691G>A
c.155G>A (p.Arg52His)
c.118G>A (p.Ala40Thr)
n.256G>A
c.109G>A (p.Ala37Thr)
n.235G>A
c.-2045G>A (n.-2045G>A)
c.-236G>A (n.-236G>A)
c.142G>A (p.Ala48Thr)
gnomAD v4
13g.23375173G>ACA482928850SACSn.690C>T
c.154C>T (p.Arg52Cys)
c.117C>T (p.Phe39=)
n.255C>T
c.108C>T (p.Phe36=)
n.234C>T
c.-2046C>T (n.-2046C>T)
c.-237C>T (n.-237C>T)
c.141C>T (p.Phe47=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.23375173G>CCA387554518SACSn.690C>G
c.154C>G (p.Arg52Gly)
c.117C>G (p.Phe39Leu)
n.255C>G
c.108C>G (p.Phe36Leu)
n.234C>G
c.-2046C>G (n.-2046C>G)
c.-237C>G (n.-237C>G)
c.141C>G (p.Phe47Leu)
gnomAD v4
13g.23375173G=CA2078656735SACSn.690C=
c.154C= (p.Arg52=)
c.117C= (p.Phe39=)
n.255C=
c.108C= (p.Phe36=)
n.234C=
c.-2046C= (n.-2046C=)
c.-237C= (n.-237C=)
c.141C= (p.Phe47=)
13g.23375173G>TCA387554516SACSn.690C>A
c.154C>A (p.Arg52Ser)
c.117C>A (p.Phe39Leu)
n.255C>A
c.108C>A (p.Phe36Leu)
n.234C>A
c.-2046C>A (n.-2046C>A)
c.-237C>A (n.-237C>A)
c.141C>A (p.Phe47Leu)
gnomAD v4
13g.23375174A>CCA387554519SACSn.689T>G
c.153T>G (p.Leu51=)
c.116T>G (p.Phe39Cys)
n.254T>G
c.107T>G (p.Phe36Cys)
n.233T>G
c.-2047T>G (n.-2047T>G)
c.-238T>G (n.-238T>G)
c.140T>G (p.Phe47Cys)
gnomAD v4
13g.23375174A>GCA387554521SACSn.689T>C
c.153T>C (p.Leu51=)
c.116T>C (p.Phe39Ser)
n.254T>C
c.107T>C (p.Phe36Ser)
n.233T>C
c.-2047T>C (n.-2047T>C)
c.-238T>C (n.-238T>C)
c.140T>C (p.Phe47Ser)
gnomAD v4
13g.23375174A>TCA387554522SACSn.689T>A
c.153T>A (p.Leu51=)
c.116T>A (p.Phe39Tyr)
n.254T>A
c.107T>A (p.Phe36Tyr)
n.233T>A
c.-2047T>A (n.-2047T>A)
c.-238T>A (n.-238T>A)
c.140T>A (p.Phe47Tyr)
13g.23375175A>CCA387554524SACSn.688T>G
c.152T>G (p.Leu51Arg)
c.115T>G (p.Phe39Val)
n.253T>G
c.106T>G (p.Phe36Val)
n.232T>G
c.-2048T>G (n.-2048T>G)
c.-239T>G (n.-239T>G)
c.139T>G (p.Phe47Val)
13g.23375175A>GCA387554526SACSn.688T>C
c.152T>C (p.Leu51Pro)
c.115T>C (p.Phe39Leu)
n.253T>C
c.106T>C (p.Phe36Leu)
n.232T>C
c.-2048T>C (n.-2048T>C)
c.-239T>C (n.-239T>C)
c.139T>C (p.Phe47Leu)
gnomAD v4
13g.23375175A>TCA387554527SACSn.688T>A
c.152T>A (p.Leu51His)
c.115T>A (p.Phe39Ile)
n.253T>A
c.106T>A (p.Phe36Ile)
n.232T>A
c.-2048T>A (n.-2048T>A)
c.-239T>A (n.-239T>A)
c.139T>A (p.Phe47Ile)
gnomAD v4
13g.23375176G>ACA482928857SACSn.687C>T
c.151C>T (p.Leu51Phe)
c.114C>T (p.Ile38=)
n.252C>T
c.105C>T (p.Ile35=)
n.231C>T
c.-2049C>T (n.-2049C>T)
c.-240C>T (n.-240C>T)
c.138C>T (p.Ile46=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.23375176G>CCA387554529SACSn.687C>G
c.151C>G (p.Leu51Val)
c.114C>G (p.Ile38Met)
n.252C>G
c.105C>G (p.Ile35Met)
n.231C>G
c.-2049C>G (n.-2049C>G)
c.-240C>G (n.-240C>G)
c.138C>G (p.Ile46Met)
13g.23375176G=CA2078656740SACSn.687C=
c.151C= (p.Leu51=)
c.114C= (p.Ile38=)
n.252C=
c.105C= (p.Ile35=)
n.231C=
c.-2049C= (n.-2049C=)
c.-240C= (n.-240C=)
c.138C= (p.Ile46=)
13g.23375176G>TCA482928859SACSn.687C>A
c.151C>A (p.Leu51Ile)
c.114C>A (p.Ile38=)
n.252C>A
c.105C>A (p.Ile35=)
n.231C>A
c.-2049C>A (n.-2049C>A)
c.-240C>A (n.-240C>A)
c.138C>A (p.Ile46=)
gnomAD v4
13g.23375177A>CCA387554531SACSn.686T>G
c.150T>G (p.Tyr50Ter)
c.113T>G (p.Ile38Ser)
n.251T>G
c.104T>G (p.Ile35Ser)
n.230T>G
c.-2050T>G (n.-2050T>G)
c.-241T>G (n.-241T>G)
c.137T>G (p.Ile46Ser)
gnomAD v4
13g.23375177A>GCA387554532SACSn.686T>C
c.150T>C (p.Tyr50=)
c.113T>C (p.Ile38Thr)
n.251T>C
c.104T>C (p.Ile35Thr)
n.230T>C
c.-2050T>C (n.-2050T>C)
c.-241T>C (n.-241T>C)
c.137T>C (p.Ile46Thr)
gnomAD v4
13g.23375177A>TCA387554534SACSn.686T>A
c.150T>A (p.Tyr50Ter)
c.113T>A (p.Ile38Asn)
n.251T>A
c.104T>A (p.Ile35Asn)
n.230T>A
c.-2050T>A (n.-2050T>A)
c.-241T>A (n.-241T>A)
c.137T>A (p.Ile46Asn)
13g.23375178T>ACA387554535SACSn.685A>T
c.149A>T (p.Tyr50Phe)
c.112A>T (p.Ile38Phe)
n.250A>T
c.103A>T (p.Ile35Phe)
n.229A>T
c.-2051A>T (n.-2051A>T)
c.-242A>T (n.-242A>T)
c.136A>T (p.Ile46Phe)
13g.23375178T>CCA387554536SACSn.685A>G
c.149A>G (p.Tyr50Cys)
c.112A>G (p.Ile38Val)
n.250A>G
c.103A>G (p.Ile35Val)
n.229A>G
c.-2051A>G (n.-2051A>G)
c.-242A>G (n.-242A>G)
c.136A>G (p.Ile46Val)
gnomAD v4
13g.23375178T>GCA387554538SACSn.685A>C
c.149A>C (p.Tyr50Ser)
c.112A>C (p.Ile38Leu)
n.250A>C
c.103A>C (p.Ile35Leu)
n.229A>C
c.-2051A>C (n.-2051A>C)
c.-242A>C (n.-242A>C)
c.136A>C (p.Ile46Leu)
13g.23375178_23375180delinsTACCA2078656743SACSn.683_685delinsGTA
c.147_149delinsGTA (p.Thr49=)
c.110_112delinsGTA (p.Arg37=)
n.248_250delinsGTA
c.101_103delinsGTA (p.Arg34=)
n.227_229delinsGTA
c.-2053_-2051delinsGTA (n.-2053_-2051delinsGTA)
c.-244_-242delinsGTA (n.-244_-242delinsGTA)
c.134_136delinsGTA (p.Arg45=)
13g.23375179A>CCA482928867SACSn.684T>G
c.148T>G (p.Tyr50Asp)
c.111T>G (p.Arg37=)
n.249T>G
c.102T>G (p.Arg34=)
n.228T>G
c.-2052T>G (n.-2052T>G)
c.-243T>G (n.-243T>G)
c.135T>G (p.Arg45=)
13g.23375179A>GCA482928868SACSn.684T>C
c.148T>C (p.Tyr50His)
c.111T>C (p.Arg37=)
n.249T>C
c.102T>C (p.Arg34=)
n.228T>C
c.-2052T>C (n.-2052T>C)
c.-243T>C (n.-243T>C)
c.135T>C (p.Arg45=)
gnomAD v4
13g.23375179A>TCA482928870SACSn.684T>A
c.148T>A (p.Tyr50Asn)
c.111T>A (p.Arg37=)
n.249T>A
c.102T>A (p.Arg34=)
n.228T>A
c.-2052T>A (n.-2052T>A)
c.-243T>A (n.-243T>A)
c.135T>A (p.Arg45=)
13g.23375179_23375180delCA608985353SACSn.683_684del
c.147_148del (p.Tyr50SerfsTer?)
c.110_111del (p.Arg37HisfsTer23)
n.248_249del
c.101_102del (p.Arg34HisfsTer23)
n.227_228del
c.-2053_-2052del (n.-2053_-2052del)
c.-244_-243del (n.-244_-243del)
c.134_135del (p.Arg45HisfsTer23)
dbSNP gnomAD v2 gnomAD v4

Number of alleles fetched