Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.99622471A=CA1994941845CNTN5c.55+66202A= (n.55+66202A=)
n.559+66202A=
11g.99622471A>GCA476518976CNTN5c.55+66202A>G (n.55+66202A>G)
n.559+66202A>G
dbSNP gnomAD v3 gnomAD v4
11g.99622472C=CA1994941847CNTN5c.55+66203C= (n.55+66203C=)
n.559+66203C=
11g.99622472C>GCA601568301CNTN5c.55+66203C>G (n.55+66203C>G)
n.559+66203C>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.99622473A>CCA2724895080CNTN5c.55+66204A>C (n.55+66204A>C)
n.559+66204A>C
dbSNP
11g.99622474A=CA1994941849CNTN5c.55+66205A= (n.55+66205A=)
n.559+66205A=
11g.99622474A>TCA1994941851CNTN5c.55+66205A>T (n.55+66205A>T)
n.559+66205A>T
dbSNP
11g.99622475A=CA1994941857CNTN5c.55+66206A= (n.55+66206A=)
n.559+66206A=
11g.99622475A>GCA1994941855CNTN5c.55+66206A>G (n.55+66206A>G)
n.559+66206A>G
dbSNP
11g.99622477T>CCA1994941861CNTN5c.55+66208T>C (n.55+66208T>C)
n.559+66208T>C
dbSNP
11g.99622477T=CA1994941860CNTN5c.55+66208T= (n.55+66208T=)
n.559+66208T=
11g.99622478A>GCA2793342574CNTN5c.55+66209A>G (n.55+66209A>G)
n.559+66209A>G
11g.99622483A=CA1994941863CNTN5c.55+66214A= (n.55+66214A=)
n.559+66214A=
11g.99622483A>GCA682570852CNTN5c.55+66214A>G (n.55+66214A>G)
n.559+66214A>G
dbSNP gnomAD v3 gnomAD v4
11g.99622488G=CA1994941864CNTN5c.55+66219G= (n.55+66219G=)
n.559+66219G=
11g.99622488G>TCA1994941865CNTN5c.55+66219G>T (n.55+66219G>T)
n.559+66219G>T
dbSNP gnomAD v3 gnomAD v4
11g.99622489A=CA1994941867CNTN5c.55+66220A= (n.55+66220A=)
n.559+66220A=
11g.99622489A>TCA1994941869CNTN5c.55+66220A>T (n.55+66220A>T)
n.559+66220A>T
dbSNP
11g.99622495_99622496delinsTGCA1994941873CNTN5c.55+66226_55+66227delinsTG (n.55+66226_55+66227delinsTG)
n.559+66226_559+66227delinsTG
11g.99622496G>ACA1994941878CNTN5c.55+66227G>A (n.55+66227G>A)
n.559+66227G>A
dbSNP
11g.99622496G=CA1994941877CNTN5c.55+66227G= (n.55+66227G=)
n.559+66227G=
11g.99622499delCA918951001CNTN5c.55+66230del (n.55+66230del)
n.559+66230del
dbSNP
11g.99622497G>ACA1994941883CNTN5c.55+66228G>A (n.55+66228G>A)
n.559+66228G>A
dbSNP
11g.99622497G=CA1994941882CNTN5c.55+66228G= (n.55+66228G=)
n.559+66228G=
11g.99622498G>ACA682570858CNTN5c.55+66229G>A (n.55+66229G>A)
n.559+66229G>A
dbSNP gnomAD v3 gnomAD v4
11g.99622498G=CA1994941885CNTN5c.55+66229G= (n.55+66229G=)
n.559+66229G=
11g.99622499G>ACA682570863CNTN5c.55+66230G>A (n.55+66230G>A)
n.559+66230G>A
dbSNP
11g.99622499G=CA1994941888CNTN5c.55+66230G= (n.55+66230G=)
n.559+66230G=
11g.99622499G>TCA227975259CNTN5c.55+66230G>T (n.55+66230G>T)
n.559+66230G>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.99622502G>ACA227975260CNTN5c.55+66233G>A (n.55+66233G>A)
n.559+66233G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.99622502G=CA1994941892CNTN5c.55+66233G= (n.55+66233G=)
n.559+66233G=
11g.99622504T>GCA1994941898CNTN5c.55+66235T>G (n.55+66235T>G)
n.559+66235T>G
dbSNP
11g.99622504T=CA1994941895CNTN5c.55+66235T= (n.55+66235T=)
n.559+66235T=
11g.99622506A=CA1994941900CNTN5c.55+66237A= (n.55+66237A=)
n.559+66237A=
11g.99622506A>GCA227975261CNTN5c.55+66237A>G (n.55+66237A>G)
n.559+66237A>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.99622507T>CCA1994941902CNTN5c.55+66238T>C (n.55+66238T>C)
n.559+66238T>C
dbSNP
11g.99622507T=CA1994941903CNTN5c.55+66238T= (n.55+66238T=)
n.559+66238T=
11g.99622509G>ACA1994941906CNTN5c.55+66240G>A (n.55+66240G>A)
n.559+66240G>A
dbSNP
11g.99622509G=CA1994941904CNTN5c.55+66240G= (n.55+66240G=)
n.559+66240G=
11g.99622512A=CA1994941912CNTN5c.55+66243A= (n.55+66243A=)
n.559+66243A=
11g.99622512A>GCA682570875CNTN5c.55+66243A>G (n.55+66243A>G)
n.559+66243A>G
dbSNP gnomAD v3 gnomAD v4
11g.99622514T>GCA227975262CNTN5c.55+66245T>G (n.55+66245T>G)
n.559+66245T>G
dbSNP
11g.99622514T=CA1994941916CNTN5c.55+66245T= (n.55+66245T=)
n.559+66245T=
11g.99622515G>ACA682570883CNTN5c.55+66246G>A (n.55+66246G>A)
n.559+66246G>A
dbSNP gnomAD v3 gnomAD v4
11g.99622515G=CA1994941920CNTN5c.55+66246G= (n.55+66246G=)
n.559+66246G=
11g.99622516C>ACA682570889CNTN5c.55+66247C>A (n.55+66247C>A)
n.559+66247C>A
dbSNP gnomAD v3 gnomAD v4
11g.99622516C=CA1994941924CNTN5c.55+66247C= (n.55+66247C=)
n.559+66247C=
11g.99622516C>TCA682570891CNTN5c.55+66247C>T (n.55+66247C>T)
n.559+66247C>T
dbSNP gnomAD v3 gnomAD v4
11g.99622518T>CCA1994941928CNTN5c.55+66249T>C (n.55+66249T>C)
n.559+66249T>C
dbSNP
11g.99622518T=CA1994941931CNTN5c.55+66249T= (n.55+66249T=)
n.559+66249T=

Number of alleles fetched