Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.203183677_203183681dupCA35635846CHI3L1c.426_430dup (p.Arg144LeufsTer12)
c.444_448dup (p.Arg150LeufsTer12)
dbSNP
1g.203183679C>ACA344298967CHI3L1c.427G>T (p.Gly143Ter)
c.445G>T (p.Gly149Ter)
1g.203183679C=CA2481647397CHI3L1c.427G= (p.Gly143=)
c.445G= (p.Gly149=)
1g.203183679C>GCA344298968CHI3L1c.427G>C (p.Gly143Arg)
c.445G>C (p.Gly149Arg)
dbSNP gnomAD v2 gnomAD v4
1g.203183679C>TCA344298971CHI3L1c.427G>A (p.Gly143Arg)
c.445G>A (p.Gly149Arg)
dbSNP gnomAD v2
1g.203183680A=CA2481647398CHI3L1c.426T= (p.Pro142=)
c.444T= (p.Pro148=)
1g.203183680A>CCA422634205CHI3L1c.426T>G (p.Pro142=)
c.444T>G (p.Pro148=)
gnomAD v4
1g.203183680A>GCA422634208CHI3L1c.426T>C (p.Pro142=)
c.444T>C (p.Pro148=)
dbSNP gnomAD v3 gnomAD v4 COSMIC
1g.203183680A>TCA422634210CHI3L1c.426T>A (p.Pro142=)
c.444T>A (p.Pro148=)
1g.203183681G>ACA344298974CHI3L1c.425C>T (p.Pro142Leu)
c.443C>T (p.Pro148Leu)
dbSNP gnomAD v4
1g.203183681G>CCA344298972CHI3L1c.425C>G (p.Pro142Arg)
c.443C>G (p.Pro148Arg)
gnomAD v4
1g.203183681G=CA2481647399CHI3L1c.425C= (p.Pro142=)
c.443C= (p.Pro148=)
1g.203183681G>TCA344298973CHI3L1c.425C>A (p.Pro142His)
c.443C>A (p.Pro148His)
1g.203183682G>ACA1339307CHI3L1c.424C>T (p.Pro142Ser)
c.442C>T (p.Pro148Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.203183682G>CCA344298975CHI3L1c.424C>G (p.Pro142Ala)
c.442C>G (p.Pro148Ala)
1g.203183682G=CA1145798419CHI3L1c.424C= (p.Pro142=)
c.442C= (p.Pro148=)
1g.203183682G>TCA1339308CHI3L1c.424C>A (p.Pro142Thr)
c.442C>A (p.Pro148Thr)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.203183683G>ACA422634226CHI3L1c.423C>T (p.Tyr141=)
c.441C>T (p.Tyr147=)
dbSNP gnomAD v2 gnomAD v4
1g.203183683G>CCA344298977CHI3L1c.423C>G (p.Tyr141Ter)
c.441C>G (p.Tyr147Ter)
1g.203183683G=CA2481647400CHI3L1c.423C= (p.Tyr141=)
c.441C= (p.Tyr147=)
1g.203183683G>TCA344298979CHI3L1c.423C>A (p.Tyr141Ter)
c.441C>A (p.Tyr147Ter)
1g.203183684T>ACA344298990CHI3L1c.422A>T (p.Tyr141Phe)
c.440A>T (p.Tyr147Phe)
1g.203183684T>CCA344298982CHI3L1c.422A>G (p.Tyr141Cys)
c.440A>G (p.Tyr147Cys)
1g.203183684T>GCA344298985CHI3L1c.422A>C (p.Tyr141Ser)
c.440A>C (p.Tyr147Ser)
1g.203183685A>CCA344298994CHI3L1c.421T>G (p.Tyr141Asp)
c.439T>G (p.Tyr147Asp)
1g.203183685A>GCA344298995CHI3L1c.421T>C (p.Tyr141His)
c.439T>C (p.Tyr147His)
1g.203183685A>TCA344298996CHI3L1c.421T>A (p.Tyr141Asn)
c.439T>A (p.Tyr147Asn)
1g.203183686G>ACA422634245CHI3L1c.420C>T (p.Leu140=)
c.438C>T (p.Leu146=)
1g.203183686G>CCA422634248CHI3L1c.420C>G (p.Leu140=)
c.438C>G (p.Leu146=)
dbSNP gnomAD v3 gnomAD v4
1g.203183686G=CA2481647401CHI3L1c.420C= (p.Leu140=)
c.438C= (p.Leu146=)
1g.203183686G>TCA422634251CHI3L1c.420C>A (p.Leu140=)
c.438C>A (p.Leu146=)
1g.203183687A>CCA344299009CHI3L1c.419T>G (p.Leu140Arg)
c.437T>G (p.Leu146Arg)
1g.203183687A>GCA344299010CHI3L1c.419T>C (p.Leu140Pro)
c.437T>C (p.Leu146Pro)
1g.203183687A>TCA344299011CHI3L1c.419T>A (p.Leu140His)
c.437T>A (p.Leu146His)
1g.203183688G>ACA344299013CHI3L1c.418C>T (p.Leu140Phe)
c.436C>T (p.Leu146Phe)
gnomAD v4
1g.203183688G>CCA344299014CHI3L1c.418C>G (p.Leu140Val)
c.436C>G (p.Leu146Val)
1g.203183688G>TCA344299015CHI3L1c.418C>A (p.Leu140Ile)
c.436C>A (p.Leu146Ile)
1g.203183689C>ACA344299018CHI3L1c.417G>T (p.Trp139Cys)
c.435G>T (p.Trp145Cys)
gnomAD v4
1g.203183689C>GCA344299019CHI3L1c.417G>C (p.Trp139Cys)
c.435G>C (p.Trp145Cys)
1g.203183689C>TCA344299020CHI3L1c.417G>A (p.Trp139Ter)
c.435G>A (p.Trp145Ter)
1g.203183690C>ACA344299023CHI3L1c.416G>T (p.Trp139Leu)
c.434G>T (p.Trp145Leu)
1g.203183690C>GCA344299028CHI3L1c.416G>C (p.Trp139Ser)
c.434G>C (p.Trp145Ser)
1g.203183690C>TCA344299025CHI3L1c.416G>A (p.Trp139Ter)
c.434G>A (p.Trp145Ter)
1g.203183691A>CCA344299032CHI3L1c.415T>G (p.Trp139Gly)
c.433T>G (p.Trp145Gly)
1g.203183691A>GCA344299037CHI3L1c.415T>C (p.Trp139Arg)
c.433T>C (p.Trp145Arg)
1g.203183691A>TCA344299034CHI3L1c.415T>A (p.Trp139Arg)
c.433T>A (p.Trp145Arg)
1g.203183692G>ACA422634282CHI3L1c.414C>T (p.Ala138=)
c.432C>T (p.Ala144=)
dbSNP
1g.203183692G>CCA422634284CHI3L1c.414C>G (p.Ala138=)
c.432C>G (p.Ala144=)
dbSNP gnomAD v3 gnomAD v4
1g.203183692G=CA2481647402CHI3L1c.414C= (p.Ala138=)
c.432C= (p.Ala144=)
1g.203183692G>TCA422634287CHI3L1c.414C>A (p.Ala138=)
c.432C>A (p.Ala144=)

Number of alleles fetched