Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.56885317C>ACA395991522SLC12A3c.1878C>A (p.Ser626Arg)
c.1875C>A (p.Ser625Arg)
gnomAD v4
16g.56885317C>GCA395991523SLC12A3c.1878C>G (p.Ser626Arg)
c.1875C>G (p.Ser625Arg)
16g.56885317C>TCA495604648SLC12A3c.1878C>T (p.Ser626=)
c.1875C>T (p.Ser625=)
gnomAD v4
16g.56885318T>ACA8069645SLC12A3c.1879T>A (p.Tyr627Asn)
c.1876T>A (p.Tyr626Asn)
dbSNP ExAC gnomAD v2 gnomAD v4
16g.56885318T>CCA395991524SLC12A3c.1879T>C (p.Tyr627His)
c.1876T>C (p.Tyr626His)
dbSNP
16g.56885318T>GCA395991525SLC12A3c.1879T>G (p.Tyr627Asp)
c.1876T>G (p.Tyr626Asp)
16g.56885318T=CA2224356666SLC12A3c.1879T= (p.Tyr627=)
c.1876T= (p.Tyr626=)
16g.56885319A>CCA395991528SLC12A3c.1880A>C (p.Tyr627Ser)
c.1877A>C (p.Tyr626Ser)
16g.56885319A>GCA395991526SLC12A3c.1880A>G (p.Tyr627Cys)
c.1877A>G (p.Tyr626Cys)
gnomAD v4
16g.56885319A>TCA395991527SLC12A3c.1880A>T (p.Tyr627Phe)
c.1877A>T (p.Tyr626Phe)
gnomAD v4
16g.56885320C>ACA395991529SLC12A3c.1881C>A (p.Tyr627Ter)
c.1878C>A (p.Tyr626Ter)
16g.56885320C=CA2224356667SLC12A3c.1881C= (p.Tyr627=)
c.1878C= (p.Tyr626=)
16g.56885320C>GCA395991530SLC12A3c.1881C>G (p.Tyr627Ter)
c.1878C>G (p.Tyr626Ter)
16g.56885320C>TCA495604649SLC12A3c.1881C>T (p.Tyr627=)
c.1878C>T (p.Tyr626=)
ClinVar dbSNP gnomAD v4
16g.56885321T>ACA395991531SLC12A3c.1882T>A (p.Ser628Thr)
c.1879T>A (p.Ser627Thr)
gnomAD v4
16g.56885321T>CCA395991532SLC12A3c.1882T>C (p.Ser628Pro)
c.1879T>C (p.Ser627Pro)
gnomAD v4
16g.56885321T>GCA395991534SLC12A3c.1882T>G (p.Ser628Ala)
c.1879T>G (p.Ser627Ala)
16g.56885322C>ACA395991537SLC12A3c.1883C>A (p.Ser628Ter)
c.1880C>A (p.Ser627Ter)
gnomAD v4
16g.56885322C=CA2224356668SLC12A3c.1883C= (p.Ser628=)
c.1880C= (p.Ser627=)
16g.56885322C>GCA395991540SLC12A3c.1883C>G (p.Ser628Trp)
c.1880C>G (p.Ser627Trp)
16g.56885322C>TCA8069646SLC12A3c.1883C>T (p.Ser628Leu)
c.1880C>T (p.Ser627Leu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.56885323G>ACA8069647SLC12A3c.1884G>A (p.Ser628=)
c.1881G>A (p.Ser627=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.56885323G>CCA281505351SLC12A3c.1884G>C (p.Ser628=)
c.1881G>C (p.Ser627=)
dbSNP gnomAD v4
16g.56885323G=CA2224356669SLC12A3c.1884G= (p.Ser628=)
c.1881G= (p.Ser627=)
16g.56885323G>TCA495604650SLC12A3c.1884G>T (p.Ser628=)
c.1881G>T (p.Ser627=)
dbSNP gnomAD v2 gnomAD v4
16g.56885324G>ACA395991548SLC12A3c.1885G>A (p.Val629Met)
c.1882G>A (p.Val628Met)
dbSNP gnomAD v3 gnomAD v4
16g.56885324G>CCA395991550SLC12A3c.1885G>C (p.Val629Leu)
c.1882G>C (p.Val628Leu)
dbSNP gnomAD v3 gnomAD v4
16g.56885324G=CA2224356670SLC12A3c.1885G= (p.Val629=)
c.1882G= (p.Val628=)
16g.56885324G>TCA395991552SLC12A3c.1885G>T (p.Val629Leu)
c.1882G>T (p.Val628Leu)
gnomAD v4
16g.56885325T>ACA395991556SLC12A3c.1886T>A (p.Val629Glu)
c.1883T>A (p.Val628Glu)
16g.56885325T>CCA395991558SLC12A3c.1886T>C (p.Val629Ala)
c.1883T>C (p.Val628Ala)
gnomAD v4
16g.56885325T>GCA395991554SLC12A3c.1886T>G (p.Val629Gly)
c.1883T>G (p.Val628Gly)
dbSNP gnomAD v3 gnomAD v4
16g.56885325T=CA2224356671SLC12A3c.1886T= (p.Val629=)
c.1883T= (p.Val628=)
16g.56885326G>ACA495604651SLC12A3c.1887G>A (p.Val629=)
c.1884G>A (p.Val628=)
ClinVar dbSNP gnomAD v2 gnomAD v4
16g.56885326G>CCA495604652SLC12A3c.1887G>C (p.Val629=)
c.1884G>C (p.Val628=)
16g.56885326G=CA2224356672SLC12A3c.1887G= (p.Val629=)
c.1884G= (p.Val628=)
16g.56885326G>TCA495604653SLC12A3c.1887G>T (p.Val629=)
c.1884G>T (p.Val628=)
gnomAD v4
16g.56885328delCA2633373967SLC12A3c.1889del (p.Gly630AlafsTer?)
c.1886del (p.Gly629AlafsTer?)
gnomAD v4
16g.56885327G>ACA395991561SLC12A3c.1888G>A (p.Gly630Ser)
c.1885G>A (p.Gly629Ser)
dbSNP gnomAD v2 gnomAD v4
16g.56885327G>CCA395991563SLC12A3c.1888G>C (p.Gly630Arg)
c.1885G>C (p.Gly629Arg)
16g.56885327G=CA2224356673SLC12A3c.1888G= (p.Gly630=)
c.1885G= (p.Gly629=)
16g.56885327G>TCA395991565SLC12A3c.1888G>T (p.Gly630Cys)
c.1885G>T (p.Gly629Cys)
16g.56885328G>ACA395991567SLC12A3c.1889G>A (p.Gly630Asp)
c.1886G>A (p.Gly629Asp)
gnomAD v4
16g.56885328G>CCA395991569SLC12A3c.1889G>C (p.Gly630Ala)
c.1886G>C (p.Gly629Ala)
16g.56885328G=CA2224356674SLC12A3c.1889G= (p.Gly630=)
c.1886G= (p.Gly629=)
16g.56885328G>TCA119778SLC12A3c.1889G>T (p.Gly630Val)
c.1886G>T (p.Gly629Val)
ClinVar dbSNP gnomAD v4
16g.56885329C>ACA495604654SLC12A3c.1890C>A (p.Gly630=)
c.1887C>A (p.Gly629=)
gnomAD v4
16g.56885329C>GCA495604655SLC12A3c.1890C>G (p.Gly630=)
c.1887C>G (p.Gly629=)
ClinVar
16g.56885329C>TCA495604656SLC12A3c.1890C>T (p.Gly630=)
c.1887C>T (p.Gly629=)
ClinVar dbSNP gnomAD v4
16g.56885330C>ACA395991577SLC12A3c.1891C>A (p.Leu631Ile)
c.1888C>A (p.Leu630Ile)
gnomAD v4

Number of alleles fetched