Chr Mutation (hg38) CAid Gene Transcript Linkouts
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)
 ClinVar 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)
18g.31519900A>GCA402130913DSG2n.10A>G
c.179A>G (p.Glu60Gly)
c.10A>G
c.-356A>G (n.-356A>G)
18g.31519900A>TCA402130914DSG2n.10A>T
c.179A>T (p.Glu60Val)
c.10A>T
c.-356A>T (n.-356A>T)
18g.31519901G>ACA503596831DSG2n.11G>A
c.180G>A (p.Glu60=)
c.11G>A
c.-355G>A (n.-355G>A)
 ClinVar
18g.31519901G>CCA402130915DSG2n.11G>C
c.180G>C (p.Glu60Asp)
c.11G>C
c.-355G>C (n.-355G>C)
 COSMIC
18g.31519901G>TCA402130916DSG2n.11G>T
c.180G>T (p.Glu60Asp)
c.11G>T
c.-355G>T (n.-355G>T)
18g.31519902G>ACA402130918DSG2n.12G>A
c.181G>A (p.Gly61Arg)
c.12G>A
c.-354G>A (n.-354G>A)
18g.31519902G>CCA402130920DSG2n.12G>C
c.181G>C (p.Gly61Arg)
c.12G>C
c.-354G>C (n.-354G>C)
18g.31519902G>TCA402130919DSG2n.12G>T
c.181G>T (p.Gly61Ter)
c.12G>T
c.-354G>T (n.-354G>T)
18g.31519903G>ACA402130922DSG2n.13G>A
c.182G>A (p.Gly61Glu)
c.13G>A
c.-353G>A (n.-353G>A)
18g.31519903G>CCA402130924DSG2n.13G>C
c.182G>C (p.Gly61Ala)
c.13G>C
c.-353G>C (n.-353G>C)
18g.31519903G=CA2293855001DSG2n.13G=
c.182G= (p.Gly61=)
c.13G=
c.-353G= (n.-353G=)
18g.31519903G>TCA043822DSG2n.13G>T
c.182G>T (p.Gly61Val)
c.13G>T
c.-353G>T (n.-353G>T)
 ClinVar dbSNP ExAC
18g.31519904A>CCA503596833DSG2n.14A>C
c.183A>C (p.Gly61=)
c.14A>C
c.-352A>C (n.-352A>C)
18g.31519904A>GCA503596834DSG2n.14A>G
c.183A>G (p.Gly61=)
c.14A>G
c.-352A>G (n.-352A>G)
18g.31519904A>TCA503596835DSG2n.14A>T
c.183A>T (p.Gly61=)
c.14A>T
c.-352A>T (n.-352A>T)
 gnomAD v4
18g.31519905G>ACA402130925DSG2n.15G>A
c.184G>A (p.Glu62Lys)
c.15G>A
c.-351G>A (n.-351G>A)
 dbSNP gnomAD v4

Number of alleles fetched