Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.74457273C>ACA381973668KCNE3c.291G>T (p.Lys97Asn)
c.423G>T (p.Lys141Asn)
11g.74457273C>GCA381973669KCNE3c.291G>C (p.Lys97Asn)
c.423G>C (p.Lys141Asn)
11g.74457273C>TCA475842723KCNE3c.291G>A (p.Lys97=)
c.423G>A (p.Lys141=)
gnomAD v4
11g.74457274T>ACA381973670KCNE3c.290A>T (p.Lys97Met)
c.422A>T (p.Lys141Met)
11g.74457274T>CCA381973671KCNE3c.290A>G (p.Lys97Arg)
c.422A>G (p.Lys141Arg)
gnomAD v4
11g.74457274T>GCA381973672KCNE3c.290A>C (p.Lys97Thr)
c.422A>C (p.Lys141Thr)
11g.74457275T>ACA381973673KCNE3c.289A>T (p.Lys97Ter)
c.421A>T (p.Lys141Ter)
11g.74457275T>CCA381973675KCNE3c.289A>G (p.Lys97Glu)
c.421A>G (p.Lys141Glu)
11g.74457275T>GCA381973674KCNE3c.289A>C (p.Lys97Gln)
c.421A>C (p.Lys141Gln)
dbSNP
11g.74457275T=CA1982893239KCNE3c.289A= (p.Lys97=)
c.421A= (p.Lys141=)
11g.74457276G>ACA475842728KCNE3c.288C>T (p.Ile96=)
c.420C>T (p.Ile140=)
COSMIC
11g.74457276G>CCA381973676KCNE3c.288C>G (p.Ile96Met)
c.420C>G (p.Ile140Met)
11g.74457276G>TCA475842727KCNE3c.288C>A (p.Ile96=)
c.420C>A (p.Ile140=)
11g.74457277A>CCA381973677KCNE3c.287T>G (p.Ile96Ser)
c.419T>G (p.Ile140Ser)
11g.74457277A>GCA381973678KCNE3c.287T>C (p.Ile96Thr)
c.419T>C (p.Ile140Thr)
11g.74457277A>TCA381973679KCNE3c.287T>A (p.Ile96Asn)
c.419T>A (p.Ile140Asn)
11g.74457278T>ACA381973680KCNE3c.286A>T (p.Ile96Phe)
c.418A>T (p.Ile140Phe)
dbSNP gnomAD v2 gnomAD v4
11g.74457278T>CCA381973682KCNE3c.286A>G (p.Ile96Val)
c.418A>G (p.Ile140Val)
gnomAD v4
11g.74457278T>GCA381973681KCNE3c.286A>C (p.Ile96Leu)
c.418A>C (p.Ile140Leu)
11g.74457278T=CA1982893240KCNE3c.286A= (p.Ile96=)
c.418A= (p.Ile140=)
11g.74457279A>CCA381973683KCNE3c.285T>G (p.Tyr95Ter)
c.417T>G (p.Tyr139Ter)
11g.74457279A>GCA475842730KCNE3c.285T>C (p.Tyr95=)
c.417T>C (p.Tyr139=)
11g.74457279A>TCA381973684KCNE3c.285T>A (p.Tyr95Ter)
c.417T>A (p.Tyr139Ter)
11g.74457280T>ACA381973685KCNE3c.284A>T (p.Tyr95Phe)
c.416A>T (p.Tyr139Phe)
11g.74457280T>CCA6184821KCNE3c.284A>G (p.Tyr95Cys)
c.416A>G (p.Tyr139Cys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.74457280T>GCA381973686KCNE3c.284A>C (p.Tyr95Ser)
c.416A>C (p.Tyr139Ser)
11g.74457280T=CA1982893241KCNE3c.284A= (p.Tyr95=)
c.416A= (p.Tyr139=)
11g.74457281A>CCA381973687KCNE3c.283T>G (p.Tyr95Asp)
c.415T>G (p.Tyr139Asp)
11g.74457281A>GCA381973688KCNE3c.283T>C (p.Tyr95His)
c.415T>C (p.Tyr139His)
gnomAD v4
11g.74457281A>TCA381973689KCNE3c.283T>A (p.Tyr95Asn)
c.415T>A (p.Tyr139Asn)
11g.74457282C>ACA475842732KCNE3c.282G>T (p.Val94=)
c.414G>T (p.Val138=)
dbSNP
11g.74457282C=CA1982893242KCNE3c.282G= (p.Val94=)
c.414G= (p.Val138=)
11g.74457282C>GCA475842733KCNE3c.282G>C (p.Val94=)
c.414G>C (p.Val138=)
11g.74457282C>TCA475842734KCNE3c.282G>A (p.Val94=)
c.414G>A (p.Val138=)
ClinVar gnomAD v4
11g.74457283A>CCA381973690KCNE3c.281T>G (p.Val94Gly)
c.413T>G (p.Val138Gly)
11g.74457283A>GCA381973691KCNE3c.281T>C (p.Val94Ala)
c.413T>C (p.Val138Ala)
11g.74457283A>TCA381973692KCNE3c.281T>A (p.Val94Glu)
c.413T>A (p.Val138Glu)
11g.74457283_74457284delinsACCA1982893243KCNE3c.280_281delinsGT (p.Val94=)
c.412_413delinsGT (p.Val138=)
11g.74457284delCA302002KCNE3c.280del (p.Val94CysfsTer9)
c.280del (p.Val94CysfsTer?)
c.412del (p.Val138CysfsTer9)
dbSNP gnomAD v4
11g.74457284C>ACA381973693KCNE3c.280G>T (p.Val94Leu)
c.412G>T (p.Val138Leu)
11g.74457284C=CA1982893245KCNE3c.280G= (p.Val94=)
c.412G= (p.Val138=)
11g.74457284C>GCA381973694KCNE3c.280G>C (p.Val94Leu)
c.412G>C (p.Val138Leu)
11g.74457284C>TCA381973695KCNE3c.280G>A (p.Val94Met)
c.412G>A (p.Val138Met)
dbSNP gnomAD v3 gnomAD v4
11g.74457284_74457286delinsCATCA1982893244KCNE3c.278_280delinsATG (p.His93=)
c.410_412delinsATG (p.His137=)
11g.74457285A=CA1982893246KCNE3c.279T= (p.His93=)
c.411T= (p.His137=)
11g.74457285A>CCA381973696KCNE3c.279T>G (p.His93Gln)
c.411T>G (p.His137Gln)
11g.74457285A>GCA6184822KCNE3c.279T>C (p.His93=)
c.411T>C (p.His137=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.74457285A>TCA224975649KCNE3c.279T>A (p.His93Gln)
c.411T>A (p.His137Gln)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.74457285_74457286delCA600393531KCNE3c.278_279del (p.His93ArgfsTer?)
c.410_411del (p.His137ArgfsTer?)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.74457286T>ACA381973697KCNE3c.278A>T (p.His93Leu)
c.410A>T (p.His137Leu)

Number of alleles fetched