Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.17387497T>ACA379772345KCNJ11c.334A>T (p.Met112Leu)
c.595A>T (p.Met199Leu)
n.753A>T
11g.17387497T>CCA379772349KCNJ11c.334A>G (p.Met112Val)
c.595A>G (p.Met199Val)
n.753A>G
gnomAD v4
11g.17387497T>GCA379772352KCNJ11c.334A>C (p.Met112Leu)
c.595A>C (p.Met199Leu)
n.753A>C
11g.17387498G>ACA473515421KCNJ11c.333C>T (p.Phe111=)
c.594C>T (p.Phe198=)
n.752C>T
COSMIC
11g.17387498G>CCA379772355KCNJ11c.333C>G (p.Phe111Leu)
c.594C>G (p.Phe198Leu)
n.752C>G
11g.17387498G>TCA379772356KCNJ11c.333C>A (p.Phe111Leu)
c.594C>A (p.Phe198Leu)
n.752C>A
11g.17387499A>CCA379772365KCNJ11c.332T>G (p.Phe111Cys)
c.593T>G (p.Phe198Cys)
n.751T>G
11g.17387499A>GCA379772368KCNJ11c.332T>C (p.Phe111Ser)
c.593T>C (p.Phe198Ser)
n.751T>C
11g.17387499A>TCA379772361KCNJ11c.332T>A (p.Phe111Tyr)
c.593T>A (p.Phe198Tyr)
n.751T>A
11g.17387500A=CA1955119282KCNJ11c.331T= (p.Phe111=)
c.592T= (p.Phe198=)
n.750T=
11g.17387500A>CCA379772371KCNJ11c.331T>G (p.Phe111Val)
c.592T>G (p.Phe198Val)
n.750T>G
dbSNP
11g.17387500A>GCA379772372KCNJ11c.331T>C (p.Phe111Leu)
c.592T>C (p.Phe198Leu)
n.750T>C
11g.17387500A>TCA379772373KCNJ11c.331T>A (p.Phe111Ile)
c.592T>A (p.Phe198Ile)
n.750T>A
11g.17387501G>ACA473515424KCNJ11c.330C>T (p.Cys110=)
c.591C>T (p.Cys197=)
n.749C>T
11g.17387501G>CCA379772377KCNJ11c.330C>G (p.Cys110Trp)
c.591C>G (p.Cys197Trp)
n.749C>G
11g.17387501G>TCA379772380KCNJ11c.330C>A (p.Cys110Ter)
c.591C>A (p.Cys197Ter)
n.749C>A
11g.17387502C>ACA379772385KCNJ11c.329G>T (p.Cys110Phe)
c.590G>T (p.Cys197Phe)
n.748G>T
11g.17387502C=CA1955119283KCNJ11c.329G= (p.Cys110=)
c.590G= (p.Cys197=)
n.748G=
11g.17387502C>GCA379772389KCNJ11c.329G>C (p.Cys110Ser)
c.590G>C (p.Cys197Ser)
n.748G>C
11g.17387502C>TCA379772390KCNJ11c.329G>A (p.Cys110Tyr)
c.590G>A (p.Cys197Tyr)
n.748G>A
dbSNP gnomAD v2
11g.17387503A>CCA379772392KCNJ11c.328T>G (p.Cys110Gly)
c.589T>G (p.Cys197Gly)
n.747T>G
11g.17387503A>GCA379772395KCNJ11c.328T>C (p.Cys110Arg)
c.589T>C (p.Cys197Arg)
n.747T>C
11g.17387503A>TCA379772399KCNJ11c.328T>A (p.Cys110Ser)
c.589T>A (p.Cys197Ser)
n.747T>A
11g.17387504G>ACA473515426KCNJ11c.327C>T (p.Leu109=)
c.588C>T (p.Leu196=)
n.746C>T
11g.17387504G>CCA473515427KCNJ11c.327C>G (p.Leu109=)
c.588C>G (p.Leu196=)
n.746C>G
dbSNP
11g.17387504G=CA1955119284KCNJ11c.327C= (p.Leu109=)
c.588C= (p.Leu196=)
n.746C=
11g.17387504G>TCA473515428KCNJ11c.327C>A (p.Leu109=)
c.588C>A (p.Leu196=)
n.746C>A
gnomAD v4
11g.17387505A>CCA379772410KCNJ11c.326T>G (p.Leu109Arg)
c.587T>G (p.Leu196Arg)
n.745T>G
11g.17387505A>GCA379772407KCNJ11c.326T>C (p.Leu109Pro)
c.587T>C (p.Leu196Pro)
n.745T>C
11g.17387505A>TCA379772403KCNJ11c.326T>A (p.Leu109His)
c.587T>A (p.Leu196His)
n.745T>A
11g.17387505_17387508delinsAGGCCA1955119285KCNJ11c.323_326delinsGCCT (p.Arg108=)
c.584_587delinsGCCT (p.Arg195=)
n.742_745delinsGCCT
11g.17387506G>ACA379772415KCNJ11c.325C>T (p.Leu109Phe)
c.586C>T (p.Leu196Phe)
n.744C>T
gnomAD v4
11g.17387506G>CCA379772416KCNJ11c.325C>G (p.Leu109Val)
c.586C>G (p.Leu196Val)
n.744C>G
11g.17387506G>TCA379772418KCNJ11c.325C>A (p.Leu109Ile)
c.586C>A (p.Leu196Ile)
n.744C>A
gnomAD v4
11g.17387509_17387511delCA10604675KCNJ11c.323_325del (p.Arg108del)
c.584_586del (p.Arg195del)
n.742_744del
dbSNP
11g.17387507G>ACA473515430KCNJ11c.324C>T (p.Arg108=)
c.585C>T (p.Arg195=)
n.743C>T
11g.17387507G>CCA473515432KCNJ11c.324C>G (p.Arg108=)
c.585C>G (p.Arg195=)
n.743C>G
11g.17387507G>TCA473515433KCNJ11c.324C>A (p.Arg108=)
c.585C>A (p.Arg195=)
n.743C>A
11g.17387508C>ACA379772431KCNJ11c.323G>T (p.Arg108Leu)
c.584G>T (p.Arg195Leu)
n.742G>T
gnomAD v4
11g.17387508C=CA1955119286KCNJ11c.323G= (p.Arg108=)
c.584G= (p.Arg195=)
n.742G=
11g.17387508C>GCA379772433KCNJ11c.323G>C (p.Arg108Pro)
c.584G>C (p.Arg195Pro)
n.742G>C
11g.17387508C>TCA172338KCNJ11c.323G>A (p.Arg108His)
c.584G>A (p.Arg195His)
n.742G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.17387509G>ACA5902275KCNJ11c.322C>T (p.Arg108Cys)
c.583C>T (p.Arg195Cys)
n.741C>T
dbSNP ExAC gnomAD v2 gnomAD v4
11g.17387509G>CCA379772444KCNJ11c.322C>G (p.Arg108Gly)
c.583C>G (p.Arg195Gly)
n.741C>G
11g.17387509G=CA1955119287KCNJ11c.322C= (p.Arg108=)
c.583C= (p.Arg195=)
n.741C=
11g.17387509G>TCA379772446KCNJ11c.322C>A (p.Arg108Ser)
c.583C>A (p.Arg195Ser)
n.741C>A
gnomAD v4
11g.17387510G>ACA473515436KCNJ11c.321C>T (p.Gly107=)
c.582C>T (p.Gly194=)
n.740C>T
11g.17387510G>CCA473515439KCNJ11c.321C>G (p.Gly107=)
c.582C>G (p.Gly194=)
n.740C>G
11g.17387510G>TCA473515437KCNJ11c.321C>A (p.Gly107=)
c.582C>A (p.Gly194=)
n.740C>A
gnomAD v4
11g.17387511C>ACA379772453KCNJ11c.320G>T (p.Gly107Val)
c.581G>T (p.Gly194Val)
n.739G>T

Number of alleles fetched