Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.11750066C=CA1764081006GATA4c.787-45C= (p.=)
c.784-45C= (p.=)
c.166-45C= (p.=)
n.781-45C= (p.=)
c.165+981C= (p.=)
8g.11750066C>TCA1110739924GATA4c.787-45C>T (p.=)
c.784-45C>T (p.=)
c.166-45C>T (p.=)
n.781-45C>T (p.=)
c.165+981C>T (p.=)
8g.11750067A=CA1764081008GATA4c.787-44A= (p.=)
c.784-44A= (p.=)
c.166-44A= (p.=)
n.781-44A= (p.=)
c.165+982A= (p.=)
8g.11750067A>GCA4630691GATA4c.787-44A>G (p.=)
c.784-44A>G (p.=)
c.166-44A>G (p.=)
n.781-44A>G (p.=)
c.165+982A>G (p.=)
dbSNP ExAC gnomAD
8g.11750068C=CA1764081011GATA4c.787-43C= (p.=)
c.784-43C= (p.=)
c.166-43C= (p.=)
n.781-43C= (p.=)
c.165+983C= (p.=)
8g.11750068C>TCA579787809GATA4c.787-43C>T (p.=)
c.784-43C>T (p.=)
c.166-43C>T (p.=)
n.781-43C>T (p.=)
c.165+983C>T (p.=)
gnomAD
8g.11750069A=CA1764081015GATA4c.787-42A= (p.=)
c.784-42A= (p.=)
c.166-42A= (p.=)
n.781-42A= (p.=)
c.165+984A= (p.=)
8g.11750069A>CCA1110739926GATA4c.787-42A>C (p.=)
c.784-42A>C (p.=)
c.166-42A>C (p.=)
n.781-42A>C (p.=)
c.165+984A>C (p.=)
8g.11750069A>GCA4630692GATA4c.787-42A>G (p.=)
c.784-42A>G (p.=)
c.166-42A>G (p.=)
n.781-42A>G (p.=)
c.165+984A>G (p.=)
dbSNP ExAC gnomAD
8g.11750070C=CA1764081017GATA4c.787-41C= (p.=)
c.784-41C= (p.=)
c.166-41C= (p.=)
n.781-41C= (p.=)
c.165+985C= (p.=)
8g.11750070C>TCA4630693GATA4c.787-41C>T (p.=)
c.784-41C>T (p.=)
c.166-41C>T (p.=)
n.781-41C>T (p.=)
c.165+985C>T (p.=)
dbSNP ExAC gnomAD
8g.11750071C=CA1764081019GATA4c.787-40C= (p.=)
c.784-40C= (p.=)
c.166-40C= (p.=)
n.781-40C= (p.=)
c.165+986C= (p.=)
8g.11750071C>GCA579787815GATA4c.787-40C>G (p.=)
c.784-40C>G (p.=)
c.166-40C>G (p.=)
n.781-40C>G (p.=)
c.165+986C>G (p.=)
gnomAD
8g.11750077C=CA1764081021GATA4c.787-34C= (p.=)
c.784-34C= (p.=)
c.166-34C= (p.=)
n.781-34C= (p.=)
c.165+992C= (p.=)
8g.11750077C>TCA4630694GATA4c.787-34C>T (p.=)
c.784-34C>T (p.=)
c.166-34C>T (p.=)
n.781-34C>T (p.=)
c.165+992C>T (p.=)
dbSNP ExAC gnomAD
8g.11750078T>CCA4630695GATA4c.787-33T>C (p.=)
c.784-33T>C (p.=)
c.166-33T>C (p.=)
n.781-33T>C (p.=)
c.165+993T>C (p.=)
ExAC gnomAD
8g.11750078T>GCA370312895GATA4c.787-33T>G (p.=)
c.784-33T>G (p.=)
c.166-33T>G (p.=)
n.781-33T>G (p.=)
c.165+993T>G (p.=)
gnomAD
8g.11750078T=CA1764081024GATA4c.787-33T= (p.=)
c.784-33T= (p.=)
c.166-33T= (p.=)
n.781-33T= (p.=)
c.165+993T= (p.=)
8g.11750081G=CA1764081026GATA4c.787-30G= (p.=)
c.784-30G= (p.=)
c.166-30G= (p.=)
n.781-30G= (p.=)
c.165+996G= (p.=)
8g.11750081G>TCA1764081027GATA4c.787-30G>T (p.=)
c.784-30G>T (p.=)
c.166-30G>T (p.=)
n.781-30G>T (p.=)
c.165+996G>T (p.=)
8g.11750082A=CA1764081029GATA4c.787-29A= (p.=)
c.784-29A= (p.=)
c.166-29A= (p.=)
n.781-29A= (p.=)
c.165+997A= (p.=)
8g.11750082A>GCA4630696GATA4c.787-29A>G (p.=)
c.784-29A>G (p.=)
c.166-29A>G (p.=)
n.781-29A>G (p.=)
c.165+997A>G (p.=)
dbSNP ExAC gnomAD
8g.11750083C>ACA846154937GATA4c.787-28C>A (p.=)
c.784-28C>A (p.=)
c.166-28C>A (p.=)
n.781-28C>A (p.=)
c.165+998C>A (p.=)
8g.11750083C=CA1764081030GATA4c.787-28C= (p.=)
c.784-28C= (p.=)
c.166-28C= (p.=)
n.781-28C= (p.=)
c.165+998C= (p.=)
8g.11750084A=CA1764081032GATA4c.787-27A= (p.=)
c.784-27A= (p.=)
c.166-27A= (p.=)
n.781-27A= (p.=)
c.165+999A= (p.=)
8g.11750084A>GCA4630697GATA4c.787-27A>G (p.=)
c.784-27A>G (p.=)
c.166-27A>G (p.=)
n.781-27A>G (p.=)
c.165+999A>G (p.=)
dbSNP ExAC gnomAD
8g.11750084A>TCA1764081033GATA4c.787-27A>T (p.=)
c.784-27A>T (p.=)
c.166-27A>T (p.=)
n.781-27A>T (p.=)
c.165+999A>T (p.=)
8g.11750085T>CCA4630698GATA4c.787-26T>C (p.=)
c.784-26T>C (p.=)
c.166-26T>C (p.=)
n.781-26T>C (p.=)
c.165+1000T>C (p.=)
dbSNP ExAC gnomAD
8g.11750085T=CA1764081036GATA4c.787-26T= (p.=)
c.784-26T= (p.=)
c.166-26T= (p.=)
n.781-26T= (p.=)
c.165+1000T= (p.=)
8g.11750086G>ACA579787821GATA4c.787-25G>A (p.=)
c.784-25G>A (p.=)
c.166-25G>A (p.=)
n.781-25G>A (p.=)
c.165+1001G>A (p.=)
gnomAD
8g.11750086G=CA1764081037GATA4c.787-25G= (p.=)
c.784-25G= (p.=)
c.166-25G= (p.=)
n.781-25G= (p.=)
c.165+1001G= (p.=)
8g.11750086G>TCA846154942GATA4c.787-25G>T (p.=)
c.784-25G>T (p.=)
c.166-25G>T (p.=)
n.781-25G>T (p.=)
c.165+1001G>T (p.=)
8g.11750089G>ACA579787823GATA4c.787-22G>A (p.=)
c.784-22G>A (p.=)
c.166-22G>A (p.=)
n.781-22G>A (p.=)
c.165+1004G>A (p.=)
gnomAD
8g.11750089G=CA1764081040GATA4c.787-22G= (p.=)
c.784-22G= (p.=)
c.166-22G= (p.=)
n.781-22G= (p.=)
c.165+1004G= (p.=)
8g.11750090C=CA1764081041GATA4c.787-21C= (p.=)
c.784-21C= (p.=)
c.166-21C= (p.=)
n.781-21C= (p.=)
c.165+1005C= (p.=)
8g.11750090C>TCA4630699GATA4c.787-21C>T (p.=)
c.784-21C>T (p.=)
c.166-21C>T (p.=)
n.781-21C>T (p.=)
c.165+1005C>T (p.=)
dbSNP ExAC gnomAD
8g.11750095G>ACA4630700GATA4c.787-16G>A (p.=)
c.784-16G>A (p.=)
c.166-16G>A (p.=)
n.781-16G>A (p.=)
c.165+1010G>A (p.=)
dbSNP ExAC gnomAD
8g.11750095G=CA1764081044GATA4c.787-16G= (p.=)
c.784-16G= (p.=)
c.166-16G= (p.=)
n.781-16G= (p.=)
c.165+1010G= (p.=)
8g.11750099C=CA1764081046GATA4c.787-12C= (p.=)
c.784-12C= (p.=)
c.166-12C= (p.=)
n.781-12C= (p.=)
c.165+1014C= (p.=)
8g.11750099C>GCA846154948GATA4c.787-12C>G (p.=)
c.784-12C>G (p.=)
c.166-12C>G (p.=)
n.781-12C>G (p.=)
c.165+1014C>G (p.=)
8g.11750099C>TCA4630701GATA4c.787-12C>T (p.=)
c.784-12C>T (p.=)
c.166-12C>T (p.=)
n.781-12C>T (p.=)
c.165+1014C>T (p.=)
dbSNP ExAC gnomAD
8g.11750100C=CA1764081048GATA4c.787-11C= (p.=)
c.784-11C= (p.=)
c.166-11C= (p.=)
n.781-11C= (p.=)
c.165+1015C= (p.=)
8g.11750100C>TCA1764081049GATA4c.787-11C>T (p.=)
c.784-11C>T (p.=)
c.166-11C>T (p.=)
n.781-11C>T (p.=)
c.165+1015C>T (p.=)
8g.11750102G>ACA1764081051GATA4c.787-9G>A (p.=)
c.784-9G>A (p.=)
c.166-9G>A (p.=)
n.781-9G>A (p.=)
c.165+1017G>A (p.=)
8g.11750102G>CCA1764081053GATA4c.787-9G>C (p.=)
c.784-9G>C (p.=)
c.166-9G>C (p.=)
n.781-9G>C (p.=)
c.165+1017G>C (p.=)
8g.11750102G=CA1764081050GATA4c.787-9G= (p.=)
c.784-9G= (p.=)
c.166-9G= (p.=)
n.781-9G= (p.=)
c.165+1017G= (p.=)
8g.11750103T>CCA846154949GATA4c.787-8T>C (p.=)
c.784-8T>C (p.=)
c.166-8T>C (p.=)
n.781-8T>C (p.=)
c.165+1018T>C (p.=)
8g.11750103T=CA1764081055GATA4c.787-8T= (p.=)
c.784-8T= (p.=)
c.166-8T= (p.=)
n.781-8T= (p.=)
c.165+1018T= (p.=)
8g.11750104C=CA1764081058GATA4c.787-7C= (p.=)
c.784-7C= (p.=)
c.166-7C= (p.=)
n.781-7C= (p.=)
c.165+1019C= (p.=)
8g.11750104C>GCA4630702GATA4c.787-7C>G (p.=)
c.784-7C>G (p.=)
c.166-7C>G (p.=)
n.781-7C>G (p.=)
c.165+1019C>G (p.=)
dbSNP ExAC gnomAD

Number of alleles fetched