Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.99622442_99622443delCA227975254CNTN5c.55+66173_55+66174del (n.55+66173_55+66174del)
n.559+66173_559+66174del
dbSNP gnomAD v3 gnomAD v4
11g.99622442C>ACA2581054243CNTN5c.55+66173C>A (n.55+66173C>A)
n.559+66173C>A
11g.99622442C=CA1994941806CNTN5c.55+66173C= (n.55+66173C=)
n.559+66173C=
11g.99622442C>GCA13490446CNTN5c.55+66173C>G (n.55+66173C>G)
n.559+66173C>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.99622442C>TCA2581054244CNTN5c.55+66173C>T (n.55+66173C>T)
n.559+66173C>T
11g.99622448A=CA1994941811CNTN5c.55+66179A= (n.55+66179A=)
n.559+66179A=
11g.99622448A>GCA682570829CNTN5c.55+66179A>G (n.55+66179A>G)
n.559+66179A>G
dbSNP
11g.99622449A=CA1994941814CNTN5c.55+66180A= (n.55+66180A=)
n.559+66180A=
11g.99622449A>CCA2724611226CNTN5c.55+66180A>C (n.55+66180A>C)
n.559+66180A>C
dbSNP
11g.99622449A>GCA682570833CNTN5c.55+66180A>G (n.55+66180A>G)
n.559+66180A>G
dbSNP
11g.99622451G=CA1994941816CNTN5c.55+66182G= (n.55+66182G=)
n.559+66182G=
11g.99622451G>TCA227975255CNTN5c.55+66182G>T (n.55+66182G>T)
n.559+66182G>T
dbSNP gnomAD v2
11g.99622453T>CCA227975256CNTN5c.55+66184T>C (n.55+66184T>C)
n.559+66184T>C
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.99622453T=CA1994941817CNTN5c.55+66184T= (n.55+66184T=)
n.559+66184T=
11g.99622456A>TCA2556998683CNTN5c.55+66187A>T (n.55+66187A>T)
n.559+66187A>T
11g.99622459C=CA1994941820CNTN5c.55+66190C= (n.55+66190C=)
n.559+66190C=
11g.99622459C>GCA682570834CNTN5c.55+66190C>G (n.55+66190C>G)
n.559+66190C>G
dbSNP gnomAD v3 gnomAD v4
11g.99622459C>TCA227975257CNTN5c.55+66190C>T (n.55+66190C>T)
n.559+66190C>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.99622460G>ACA227975258CNTN5c.55+66191G>A (n.55+66191G>A)
n.559+66191G>A
dbSNP gnomAD v3 gnomAD v4
11g.99622460G=CA1994941822CNTN5c.55+66191G= (n.55+66191G=)
n.559+66191G=
11g.99622460G>TCA1994941824CNTN5c.55+66191G>T (n.55+66191G>T)
n.559+66191G>T
dbSNP
11g.99622461G>CCA1994941827CNTN5c.55+66192G>C (n.55+66192G>C)
n.559+66192G>C
dbSNP
11g.99622461G=CA1994941825CNTN5c.55+66192G= (n.55+66192G=)
n.559+66192G=
11g.99622462_99622463delinsTACA1994941828CNTN5c.55+66193_55+66194delinsTA (n.55+66193_55+66194delinsTA)
n.559+66193_559+66194delinsTA
11g.99622463delCA1994941830CNTN5c.55+66194del (n.55+66194del)
n.559+66194del
dbSNP
11g.99622468T>GCA601568300CNTN5c.55+66199T>G (n.55+66199T>G)
n.559+66199T>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.99622468T=CA1994941834CNTN5c.55+66199T= (n.55+66199T=)
n.559+66199T=
11g.99622469C>ACA682570842CNTN5c.55+66200C>A (n.55+66200C>A)
n.559+66200C>A
dbSNP gnomAD v3 gnomAD v4
11g.99622469C=CA1994941839CNTN5c.55+66200C= (n.55+66200C=)
n.559+66200C=
11g.99622469C>TCA682570840CNTN5c.55+66200C>T (n.55+66200C>T)
n.559+66200C>T
dbSNP gnomAD v3 gnomAD v4
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.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=

Number of alleles fetched