Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.99622366G>ACA1994941715CNTN5c.55+66097G>A (n.55+66097G>A)
n.559+66097G>A
dbSNP
11g.99622366G=CA1994941713CNTN5c.55+66097G= (n.55+66097G=)
n.559+66097G=
11g.99622368T>ACA2537028881CNTN5c.55+66099T>A (n.55+66099T>A)
n.559+66099T>A
11g.99622369C>ACA227975247CNTN5c.55+66100C>A (n.55+66100C>A)
n.559+66100C>A
dbSNP
11g.99622369C=CA1994941716CNTN5c.55+66100C= (n.55+66100C=)
n.559+66100C=
11g.99622369C>GCA2793342570CNTN5c.55+66100C>G (n.55+66100C>G)
n.559+66100C>G
11g.99622370T>CCA682570796CNTN5c.55+66101T>C (n.55+66101T>C)
n.559+66101T>C
dbSNP
11g.99622370T=CA1994941724CNTN5c.55+66101T= (n.55+66101T=)
n.559+66101T=
11g.99622375T>GCA1994941729CNTN5c.55+66106T>G (n.55+66106T>G)
n.559+66106T>G
dbSNP
11g.99622375T=CA1994941728CNTN5c.55+66106T= (n.55+66106T=)
n.559+66106T=
11g.99622378A=CA1994941730CNTN5c.55+66109A= (n.55+66109A=)
n.559+66109A=
11g.99622378A>GCA1994941731CNTN5c.55+66109A>G (n.55+66109A>G)
n.559+66109A>G
dbSNP
11g.99622381T>GCA2793342571CNTN5c.55+66112T>G (n.55+66112T>G)
n.559+66112T>G
11g.99622382G>ACA682570799CNTN5c.55+66113G>A (n.55+66113G>A)
n.559+66113G>A
dbSNP gnomAD v3 gnomAD v4
11g.99622382G=CA1994941734CNTN5c.55+66113G= (n.55+66113G=)
n.559+66113G=
11g.99622386T>CCA682570801CNTN5c.55+66117T>C (n.55+66117T>C)
n.559+66117T>C
dbSNP
11g.99622386T=CA1994941735CNTN5c.55+66117T= (n.55+66117T=)
n.559+66117T=
11g.99622386_99622387delinsTGCA1994941736CNTN5c.55+66117_55+66118delinsTG (n.55+66117_55+66118delinsTG)
n.559+66117_559+66118delinsTG
11g.99622387G>ACA1994941743CNTN5c.55+66118G>A (n.55+66118G>A)
n.559+66118G>A
dbSNP
11g.99622387G=CA1994941739CNTN5c.55+66118G= (n.55+66118G=)
n.559+66118G=
11g.99622388delCA1994941738CNTN5c.55+66119del (n.55+66119del)
n.559+66119del
dbSNP
11g.99622388G=CA1994941745CNTN5c.55+66119G= (n.55+66119G=)
n.559+66119G=
11g.99622388G>TCA227975248CNTN5c.55+66119G>T (n.55+66119G>T)
n.559+66119G>T
dbSNP gnomAD v3 gnomAD v4
11g.99622388_99622389delinsGACA1994941749CNTN5c.55+66119_55+66120delinsGA (n.55+66119_55+66120delinsGA)
n.559+66119_559+66120delinsGA
11g.99622391delCA682570807CNTN5c.55+66122del (n.55+66122del)
n.559+66122del
dbSNP gnomAD v3 gnomAD v4
11g.99622393A=CA1994941750CNTN5c.55+66124A= (n.55+66124A=)
n.559+66124A=
11g.99622393A>GCA682570808CNTN5c.55+66124A>G (n.55+66124A>G)
n.559+66124A>G
dbSNP
11g.99622403G>CCA1994941753CNTN5c.55+66134G>C (n.55+66134G>C)
n.559+66134G>C
dbSNP
11g.99622403G=CA1994941751CNTN5c.55+66134G= (n.55+66134G=)
n.559+66134G=
11g.99622404T>CCA227975249CNTN5c.55+66135T>C (n.55+66135T>C)
n.559+66135T>C
dbSNP
11g.99622404T=CA1994941756CNTN5c.55+66135T= (n.55+66135T=)
n.559+66135T=
11g.99622405C>ACA227975250CNTN5c.55+66136C>A (n.55+66136C>A)
n.559+66136C>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.99622405C=CA1994941758CNTN5c.55+66136C= (n.55+66136C=)
n.559+66136C=
11g.99622405C>TCA227975251CNTN5c.55+66136C>T (n.55+66136C>T)
n.559+66136C>T
dbSNP gnomAD v3 gnomAD v4
11g.99622406T>CCA1994941762CNTN5c.55+66137T>C (n.55+66137T>C)
n.559+66137T>C
dbSNP
11g.99622406T=CA1994941761CNTN5c.55+66137T= (n.55+66137T=)
n.559+66137T=
11g.99622407A=CA1994941765CNTN5c.55+66138A= (n.55+66138A=)
n.559+66138A=
11g.99622407A>GCA1994941768CNTN5c.55+66138A>G (n.55+66138A>G)
n.559+66138A>G
dbSNP
11g.99622409A=CA1994941772CNTN5c.55+66140A= (n.55+66140A=)
n.559+66140A=
11g.99622409A>GCA1994941770CNTN5c.55+66140A>G (n.55+66140A>G)
n.559+66140A>G
dbSNP
11g.99622410G=CA1994941774CNTN5c.55+66141G= (n.55+66141G=)
n.559+66141G=
11g.99622410G>TCA227975252CNTN5c.55+66141G>T (n.55+66141G>T)
n.559+66141G>T
dbSNP
11g.99622412G>CCA1994941778CNTN5c.55+66143G>C (n.55+66143G>C)
n.559+66143G>C
dbSNP
11g.99622412G=CA1994941777CNTN5c.55+66143G= (n.55+66143G=)
n.559+66143G=
11g.99622413A>TCA2601727327CNTN5c.55+66144A>T (n.55+66144A>T)
n.559+66144A>T
dbSNP gnomAD v3 gnomAD v4
11g.99622415A>CCA2724895032CNTN5c.55+66146A>C (n.55+66146A>C)
n.559+66146A>C
dbSNP
11g.99622416A=CA1994941783CNTN5c.55+66147A= (n.55+66147A=)
n.559+66147A=
11g.99622416A>CCA682570816CNTN5c.55+66147A>C (n.55+66147A>C)
n.559+66147A>C
dbSNP
11g.99622416A>GCA601568294CNTN5c.55+66147A>G (n.55+66147A>G)
n.559+66147A>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.99622418G=CA1994941786CNTN5c.55+66149G= (n.55+66149G=)
n.559+66149G=

Number of alleles fetched