Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.99622242A=CA1994941504CNTN5c.55+65973A= (n.55+65973A=)
n.559+65973A=
11g.99622242A>GCA227975231CNTN5c.55+65973A>G (n.55+65973A>G)
n.559+65973A>G
dbSNP
11g.99622242A>TCA682570715CNTN5c.55+65973A>T (n.55+65973A>T)
n.559+65973A>T
dbSNP gnomAD v3 gnomAD v4
11g.99622243T>CCA682570718CNTN5c.55+65974T>C (n.55+65974T>C)
n.559+65974T>C
dbSNP gnomAD v3 gnomAD v4
11g.99622243T=CA1994941505CNTN5c.55+65974T= (n.55+65974T=)
n.559+65974T=
11g.99622244A=CA1994941507CNTN5c.55+65975A= (n.55+65975A=)
n.559+65975A=
11g.99622244A>GCA1994941508CNTN5c.55+65975A>G (n.55+65975A>G)
n.559+65975A>G
dbSNP
11g.99622250A=CA1994941509CNTN5c.55+65981A= (n.55+65981A=)
n.559+65981A=
11g.99622250A>CCA1994941510CNTN5c.55+65981A>C (n.55+65981A>C)
n.559+65981A>C
dbSNP
11g.99622251C>ACA2724587802CNTN5c.55+65982C>A (n.55+65982C>A)
n.559+65982C>A
dbSNP
11g.99622251C=CA1994941512CNTN5c.55+65982C= (n.55+65982C=)
n.559+65982C=
11g.99622251C>TCA227975232CNTN5c.55+65982C>T (n.55+65982C>T)
n.559+65982C>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.99622252G>ACA601568273CNTN5c.55+65983G>A (n.55+65983G>A)
n.559+65983G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.99622252G=CA1994941514CNTN5c.55+65983G= (n.55+65983G=)
n.559+65983G=
11g.99622252G>TCA601568275CNTN5c.55+65983G>T (n.55+65983G>T)
n.559+65983G>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.99622253A=CA1994941516CNTN5c.55+65984A= (n.55+65984A=)
n.559+65984A=
11g.99622253A>GCA682570733CNTN5c.55+65984A>G (n.55+65984A>G)
n.559+65984A>G
dbSNP gnomAD v3 gnomAD v4
11g.99622253A>TCA654550199CNTN5c.55+65984A>T (n.55+65984A>T)
n.559+65984A>T
COSMIC
11g.99622258A=CA1994941518CNTN5c.55+65989A= (n.55+65989A=)
n.559+65989A=
11g.99622258A>CCA1994941519CNTN5c.55+65989A>C (n.55+65989A>C)
n.559+65989A>C
dbSNP
11g.99622262A=CA1994941521CNTN5c.55+65993A= (n.55+65993A=)
n.559+65993A=
11g.99622262A>GCA601568277CNTN5c.55+65993A>G (n.55+65993A>G)
n.559+65993A>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.99622264A=CA1994941525CNTN5c.55+65995A= (n.55+65995A=)
n.559+65995A=
11g.99622264A>GCA1994941526CNTN5c.55+65995A>G (n.55+65995A>G)
n.559+65995A>G
dbSNP
11g.99622265_99622266delinsATCA1994941528CNTN5c.55+65996_55+65997delinsAT (n.55+65996_55+65997delinsAT)
n.559+65996_559+65997delinsAT
11g.99622268delCA682570740CNTN5c.55+65999del (n.55+65999del)
n.559+65999del
dbSNP gnomAD v3 gnomAD v4
11g.99622268T>GCA1994941533CNTN5c.55+65999T>G (n.55+65999T>G)
n.559+65999T>G
dbSNP
11g.99622268T=CA1994941532CNTN5c.55+65999T= (n.55+65999T=)
n.559+65999T=
11g.99622269A=CA1994941535CNTN5c.55+66000A= (n.55+66000A=)
n.559+66000A=
11g.99622269A>GCA682570742CNTN5c.55+66000A>G (n.55+66000A>G)
n.559+66000A>G
dbSNP gnomAD v3 gnomAD v4
11g.99622270C>TCA2724894625CNTN5c.55+66001C>T (n.55+66001C>T)
n.559+66001C>T
dbSNP
11g.99622272A=CA1994941538CNTN5c.55+66003A= (n.55+66003A=)
n.559+66003A=
11g.99622272A>GCA227975233CNTN5c.55+66003A>G (n.55+66003A>G)
n.559+66003A>G
dbSNP gnomAD v3 gnomAD v4
11g.99622274A=CA1994941539CNTN5c.55+66005A= (n.55+66005A=)
n.559+66005A=
11g.99622274A>TCA1994941540CNTN5c.55+66005A>T (n.55+66005A>T)
n.559+66005A>T
dbSNP
11g.99622275C>ACA682570746CNTN5c.55+66006C>A (n.55+66006C>A)
n.559+66006C>A
dbSNP
11g.99622275C=CA1994941544CNTN5c.55+66006C= (n.55+66006C=)
n.559+66006C=
11g.99622275C>GCA1994941549CNTN5c.55+66006C>G (n.55+66006C>G)
n.559+66006C>G
dbSNP
11g.99622275C>TCA227975234CNTN5c.55+66006C>T (n.55+66006C>T)
n.559+66006C>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.99622276G>ACA227975235CNTN5c.55+66007G>A (n.55+66007G>A)
n.559+66007G>A
dbSNP gnomAD v3 gnomAD v4
11g.99622276G=CA1994941555CNTN5c.55+66007G= (n.55+66007G=)
n.559+66007G=
11g.99622280C=CA1994941559CNTN5c.55+66011C= (n.55+66011C=)
n.559+66011C=
11g.99622280C>TCA941396585CNTN5c.55+66011C>T (n.55+66011C>T)
n.559+66011C>T
dbSNP
11g.99622281T>CCA601568280CNTN5c.55+66012T>C (n.55+66012T>C)
n.559+66012T>C
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.99622281T=CA1994941562CNTN5c.55+66012T= (n.55+66012T=)
n.559+66012T=
11g.99622282G>ACA601568281CNTN5c.55+66013G>A (n.55+66013G>A)
n.559+66013G>A
dbSNP gnomAD v2
11g.99622282G=CA1994941568CNTN5c.55+66013G= (n.55+66013G=)
n.559+66013G=
11g.99622283T>ACA227975236CNTN5c.55+66014T>A (n.55+66014T>A)
n.559+66014T>A
dbSNP gnomAD v3 gnomAD v4
11g.99622283T=CA1994941571CNTN5c.55+66014T= (n.55+66014T=)
n.559+66014T=
11g.99622286T>GCA1994941574CNTN5c.55+66017T>G (n.55+66017T>G)
n.559+66017T>G
dbSNP

Number of alleles fetched