Chr Mutation (hg38) CAid Gene Transcript Linkouts
18g.31519887G>ACA021523DSG2c.166G>A (p.Val56Met)
c.-369G>A (n.-369G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.31519887G>CCA402130869DSG2c.166G>C (p.Val56Leu)
c.-369G>C (n.-369G>C)
18g.31519887G=CA2293854992DSG2c.166G= (p.Val56=)
c.-369G= (n.-369G=)
18g.31519887G>TCA402130867DSG2c.166G>T (p.Val56Leu)
c.-369G>T (n.-369G>T)
dbSNP gnomAD v3 gnomAD v4
18g.31519888T>ACA402130871DSG2c.167T>A (p.Val56Glu)
c.-368T>A (n.-368T>A)
18g.31519888T>CCA402130873DSG2c.167T>C (p.Val56Ala)
c.-368T>C (n.-368T>C)
18g.31519888T>GCA402130875DSG2c.167T>G (p.Val56Gly)
c.-368T>G (n.-368T>G)
ClinVar dbSNP gnomAD v2 gnomAD v4
18g.31519888T=CA2293854993DSG2c.167T= (p.Val56=)
c.-368T= (n.-368T=)
18g.31519889G>ACA503596807DSG2c.168G>A (p.Val56=)
c.-367G>A (n.-367G>A)
dbSNP gnomAD v2 gnomAD v4
18g.31519889G>CCA503596808DSG2c.168G>C (p.Val56=)
c.-367G>C (n.-367G>C)
18g.31519889G=CA2293854994DSG2c.168G= (p.Val56=)
c.-367G= (n.-367G=)
18g.31519889G>TCA503596809DSG2c.168G>T (p.Val56=)
c.-367G>T (n.-367G>T)
18g.31519890delCA2697555381DSG2c.169del (p.Ala57LeufsTer?)
c.-366del (n.-366del)
18g.31519890G>ACA402130877DSG2c.169G>A (p.Ala57Thr)
c.-366G>A (n.-366G>A)
gnomAD v4 COSMIC
18g.31519890G>CCA402130878DSG2c.169G>C (p.Ala57Pro)
c.-366G>C (n.-366G>C)
18g.31519890G>TCA402130880DSG2c.169G>T (p.Ala57Ser)
c.-366G>T (n.-366G>T)
18g.31519891C>ACA402130882DSG2n.1C>A
c.170C>A (p.Ala57Asp)
c.1C>A
c.-365C>A (n.-365C>A)
18g.31519891C=CA2293854995DSG2n.1C=
c.170C= (p.Ala57=)
c.1C=
c.-365C= (n.-365C=)
18g.31519891C>GCA043497DSG2n.1C>G
c.170C>G (p.Ala57Gly)
c.1C>G
c.-365C>G (n.-365C>G)
dbSNP ExAC
18g.31519891C>TCA402130885DSG2n.1C>T
c.170C>T (p.Ala57Val)
c.1C>T
c.-365C>T (n.-365C>T)
ClinVar dbSNP gnomAD v4
18g.31519892T>ACA503596812DSG2n.2T>A
c.171T>A (p.Ala57=)
c.2T>A
c.-364T>A (n.-364T>A)
gnomAD v4
18g.31519892T>CCA503596814DSG2n.2T>C
c.171T>C (p.Ala57=)
c.2T>C
c.-364T>C (n.-364T>C)
18g.31519892T>GCA503596815DSG2n.2T>G
c.171T>G (p.Ala57=)
c.2T>G
c.-364T>G (n.-364T>G)
18g.31519893C>ACA402130887DSG2n.3C>A
c.172C>A (p.Leu58Ile)
c.3C>A
c.-363C>A (n.-363C>A)
18g.31519893C=CA2293854996DSG2n.3C=
c.172C= (p.Leu58=)
c.3C=
c.-363C= (n.-363C=)
18g.31519893C>GCA402130889DSG2n.3C>G
c.172C>G (p.Leu58Val)
c.3C>G
c.-363C>G (n.-363C>G)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.31519893C>TCA043567DSG2n.3C>T
c.172C>T (p.Leu58Phe)
c.3C>T
c.-363C>T (n.-363C>T)
dbSNP ExAC gnomAD v2 gnomAD v4
18g.31519894T>ACA402130892DSG2n.4T>A
c.173T>A (p.Leu58His)
c.4T>A
c.-362T>A (n.-362T>A)
18g.31519894T>CCA402130896DSG2n.4T>C
c.173T>C (p.Leu58Pro)
c.4T>C
c.-362T>C (n.-362T>C)
18g.31519894T>GCA402130894DSG2n.4T>G
c.173T>G (p.Leu58Arg)
c.4T>G
c.-362T>G (n.-362T>G)
18g.31519895T>ACA503596819DSG2n.5T>A
c.174T>A (p.Leu58=)
c.5T>A
c.-361T>A (n.-361T>A)
18g.31519895T>CCA503596821DSG2n.5T>C
c.174T>C (p.Leu58=)
c.5T>C
c.-361T>C (n.-361T>C)
18g.31519895T>GCA503596822DSG2n.5T>G
c.174T>G (p.Leu58=)
c.5T>G
c.-361T>G (n.-361T>G)
18g.31519896C>ACA503596823DSG2n.6C>A
c.175C>A (p.Arg59=)
c.6C>A
c.-360C>A (n.-360C>A)
18g.31519896C=CA2293854997DSG2n.6C=
c.175C= (p.Arg59=)
c.6C=
c.-360C= (n.-360C=)
18g.31519896C>GCA402130898DSG2n.6C>G
c.175C>G (p.Arg59Gly)
c.6C>G
c.-360C>G (n.-360C>G)
18g.31519896C>TCA043609DSG2n.6C>T
c.175C>T (p.Arg59Trp)
c.6C>T
c.-360C>T (n.-360C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
18g.31519897G>ACA043630DSG2n.7G>A
c.176G>A (p.Arg59Gln)
c.7G>A
c.-359G>A (n.-359G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
18g.31519897G>CCA402130902DSG2n.7G>C
c.176G>C (p.Arg59Pro)
c.7G>C
c.-359G>C (n.-359G>C)
18g.31519897G=CA2293854998DSG2n.7G=
c.176G= (p.Arg59=)
c.7G=
c.-359G= (n.-359G=)
18g.31519897G>TCA402130903DSG2n.7G>T
c.176G>T (p.Arg59Leu)
c.7G>T
c.-359G>T (n.-359G>T)
18g.31519898G>ACA503596824DSG2n.8G>A
c.177G>A (p.Arg59=)
c.8G>A
c.-358G>A (n.-358G>A)
ClinVar dbSNP gnomAD v4
18g.31519898G>CCA503596826DSG2n.8G>C
c.177G>C (p.Arg59=)
c.8G>C
c.-358G>C (n.-358G>C)
ClinVar dbSNP
18g.31519898G=CA2293854999DSG2n.8G=
c.177G= (p.Arg59=)
c.8G=
c.-358G= (n.-358G=)
18g.31519898G>TCA503596828DSG2n.8G>T
c.177G>T (p.Arg59=)
c.8G>T
c.-358G>T (n.-358G>T)
18g.31519899G>ACA021560DSG2n.9G>A
c.178G>A (p.Glu60Lys)
c.9G>A
c.-357G>A (n.-357G>A)
dbSNP gnomAD v4
18g.31519899G>CCA402130907DSG2n.9G>C
c.178G>C (p.Glu60Gln)
c.9G>C
c.-357G>C (n.-357G>C)
18g.31519899G=CA2293855000DSG2n.9G=
c.178G= (p.Glu60=)
c.9G=
c.-357G= (n.-357G=)
18g.31519899G>TCA402130909DSG2n.9G>T
c.178G>T (p.Glu60Ter)
c.9G>T
c.-357G>T (n.-357G>T)
18g.31519900A>CCA402130911DSG2n.10A>C
c.179A>C (p.Glu60Ala)
c.10A>C
c.-356A>C (n.-356A>C)

Number of alleles fetched