Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.70176005G>ACA400862865KCNJ2c.966G>A (p.Trp322Ter)
17g.70176005G>CCA347403KCNJ2c.966G>C (p.Trp322Cys)
ClinVar dbSNP
17g.70176005G=CA2272996764KCNJ2c.966G= (p.Trp322=)
17g.70176005G>TCA400862867KCNJ2c.966G>T (p.Trp322Cys)
17g.70176006G>ACA400862869KCNJ2c.967G>A (p.Gly323Ser)
17g.70176006G>CCA400862871KCNJ2c.967G>C (p.Gly323Arg)
17g.70176006G>TCA400862873KCNJ2c.967G>T (p.Gly323Cys)
17g.70176007G>ACA400862875KCNJ2c.968G>A (p.Gly323Asp)
17g.70176007G>CCA400862877KCNJ2c.968G>C (p.Gly323Ala)
17g.70176007G>TCA400862879KCNJ2c.968G>T (p.Gly323Val)
17g.70176008C>ACA501700905KCNJ2c.969C>A (p.Gly323=)
17g.70176008C>GCA501700907KCNJ2c.969C>G (p.Gly323=)
17g.70176008C>TCA501700909KCNJ2c.969C>T (p.Gly323=)
17g.70176009C>ACA400862881KCNJ2c.970C>A (p.His324Asn)
17g.70176009C>GCA400862883KCNJ2c.970C>G (p.His324Asp)
17g.70176009C>TCA400862885KCNJ2c.970C>T (p.His324Tyr)
17g.70176010A>CCA400862887KCNJ2c.971A>C (p.His324Pro)
17g.70176010A>GCA400862891KCNJ2c.971A>G (p.His324Arg)
17g.70176010A>TCA400862889KCNJ2c.971A>T (p.His324Leu)
17g.70176011C>ACA400862893KCNJ2c.972C>A (p.His324Gln)
17g.70176011C=CA2272996765KCNJ2c.972C= (p.His324=)
17g.70176011C>GCA400862896KCNJ2c.972C>G (p.His324Gln)
17g.70176011C>TCA8738781KCNJ2c.972C>T (p.His324=)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.70176012C>ACA400862898KCNJ2c.973C>A (p.Arg325Ser)
17g.70176012C=CA2272996766KCNJ2c.973C= (p.Arg325=)
17g.70176012C>GCA400862900KCNJ2c.973C>G (p.Arg325Gly)
17g.70176012C>TCA302073KCNJ2c.973C>T (p.Arg325Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.70176013G>ACA400862902KCNJ2c.974G>A (p.Arg325His)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
17g.70176013G>CCA400862907KCNJ2c.974G>C (p.Arg325Pro)
17g.70176013G=CA2272996767KCNJ2c.974G= (p.Arg325=)
17g.70176013G>TCA400862909KCNJ2c.974G>T (p.Arg325Leu)
17g.70176014C>ACA501700911KCNJ2c.975C>A (p.Arg325=)
17g.70176014C>GCA501700912KCNJ2c.975C>G (p.Arg325=)
17g.70176014C>TCA501700913KCNJ2c.975C>T (p.Arg325=)
gnomAD v4
17g.70176015T>ACA302058KCNJ2c.976T>A (p.Tyr326Asn)
ClinVar dbSNP
17g.70176015T>CCA400862911KCNJ2c.976T>C (p.Tyr326His)
17g.70176015T>GCA400862912KCNJ2c.976T>G (p.Tyr326Asp)
17g.70176015T=CA2272996768KCNJ2c.976T= (p.Tyr326=)
17g.70176016A>CCA400862919KCNJ2c.977A>C (p.Tyr326Ser)
17g.70176016A>GCA400862920KCNJ2c.977A>G (p.Tyr326Cys)
17g.70176016A>TCA400862921KCNJ2c.977A>T (p.Tyr326Phe)
17g.70176017T>ACA400862924KCNJ2c.978T>A (p.Tyr326Ter)
17g.70176017T>CCA501700915KCNJ2c.978T>C (p.Tyr326=)
17g.70176017T>GCA400862926KCNJ2c.978T>G (p.Tyr326Ter)
17g.70176018G>ACA400862928KCNJ2c.979G>A (p.Glu327Lys)
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
17g.70176018G>CCA400862931KCNJ2c.979G>C (p.Glu327Gln)
17g.70176018G=CA2272996769KCNJ2c.979G= (p.Glu327=)
17g.70176018G>TCA400862930KCNJ2c.979G>T (p.Glu327Ter)
17g.70176019A>CCA400862933KCNJ2c.980A>C (p.Glu327Ala)
17g.70176019A>GCA400862935KCNJ2c.980A>G (p.Glu327Gly)

Number of alleles fetched