Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.99622223C=CA1994941486CNTN5c.55+65954C= (n.55+65954C=)
n.559+65954C=
11g.99622223C>GCA227975225CNTN5c.55+65954C>G (n.55+65954C>G)
n.559+65954C>G
dbSNP gnomAD v3 gnomAD v4
11g.99622223C>TCA227975226CNTN5c.55+65954C>T (n.55+65954C>T)
n.559+65954C>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.99622224C=CA1994941488CNTN5c.55+65955C= (n.55+65955C=)
n.559+65955C=
11g.99622224C>TCA227975227CNTN5c.55+65955C>T (n.55+65955C>T)
n.559+65955C>T
dbSNP gnomAD v3 gnomAD v4
11g.99622226A=CA1994941490CNTN5c.55+65957A= (n.55+65957A=)
n.559+65957A=
11g.99622226A>CCA1994941492CNTN5c.55+65957A>C (n.55+65957A>C)
n.559+65957A>C
dbSNP
11g.99622226A>GCA227975228CNTN5c.55+65957A>G (n.55+65957A>G)
n.559+65957A>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.99622228T>CCA682570708CNTN5c.55+65959T>C (n.55+65959T>C)
n.559+65959T>C
dbSNP gnomAD v3 gnomAD v4
11g.99622228T=CA1994941494CNTN5c.55+65959T= (n.55+65959T=)
n.559+65959T=
11g.99622231T>ACA1994941497CNTN5c.55+65962T>A (n.55+65962T>A)
n.559+65962T>A
dbSNP
11g.99622231T=CA1994941496CNTN5c.55+65962T= (n.55+65962T=)
n.559+65962T=
11g.99622232G>CCA2793342568CNTN5c.55+65963G>C (n.55+65963G>C)
n.559+65963G>C
11g.99622235G=CA1994941500CNTN5c.55+65966G= (n.55+65966G=)
n.559+65966G=
11g.99622235G>TCA227975229CNTN5c.55+65966G>T (n.55+65966G>T)
n.559+65966G>T
dbSNP
11g.99622241T>CCA227975230CNTN5c.55+65972T>C (n.55+65972T>C)
n.559+65972T>C
dbSNP
11g.99622241T=CA1994941502CNTN5c.55+65972T= (n.55+65972T=)
n.559+65972T=
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
11g.99622286T=CA1994941573CNTN5c.55+66017T= (n.55+66017T=)
n.559+66017T=
11g.99622287A>GCA941396587CNTN5c.55+66018A>G (n.55+66018A>G)
n.559+66018A>G
gnomAD v3 gnomAD v4
11g.99622299G>ACA682570757CNTN5c.55+66030G>A (n.55+66030G>A)
n.559+66030G>A
dbSNP gnomAD v3 gnomAD v4
11g.99622299G=CA1994941578CNTN5c.55+66030G= (n.55+66030G=)
n.559+66030G=
11g.99622300C>ACA941396590CNTN5c.55+66031C>A (n.55+66031C>A)
n.559+66031C>A
dbSNP gnomAD v3 gnomAD v4
11g.99622300C=CA1994941585CNTN5c.55+66031C= (n.55+66031C=)
n.559+66031C=
11g.99622301T>ACA2552046007CNTN5c.55+66032T>A (n.55+66032T>A)
n.559+66032T>A
11g.99622303G=CA1994941589CNTN5c.55+66034G= (n.55+66034G=)
n.559+66034G=
11g.99622303G>TCA227975237CNTN5c.55+66034G>T (n.55+66034G>T)
n.559+66034G>T
dbSNP gnomAD v3 gnomAD v4
11g.99622306A=CA1994941594CNTN5c.55+66037A= (n.55+66037A=)
n.559+66037A=
11g.99622306A>GCA1994941592CNTN5c.55+66037A>G (n.55+66037A>G)
n.559+66037A>G
dbSNP
11g.99622307T>CCA2537479918CNTN5c.55+66038T>C (n.55+66038T>C)
n.559+66038T>C
11g.99622307T>GCA227975238CNTN5c.55+66038T>G (n.55+66038T>G)
n.559+66038T>G
dbSNP
11g.99622307T=CA1994941600CNTN5c.55+66038T= (n.55+66038T=)
n.559+66038T=
11g.99622308C>ACA682570763CNTN5c.55+66039C>A (n.55+66039C>A)
n.559+66039C>A
dbSNP
11g.99622308C=CA1994941606CNTN5c.55+66039C= (n.55+66039C=)
n.559+66039C=
11g.99622308C>TCA1994941609CNTN5c.55+66039C>T (n.55+66039C>T)
n.559+66039C>T
dbSNP
11g.99622310A=CA1994941613CNTN5c.55+66041A= (n.55+66041A=)
n.559+66041A=
11g.99622310A>GCA601568283CNTN5c.55+66041A>G (n.55+66041A>G)
n.559+66041A>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.99622310_99622311delinsATCA1994941617CNTN5c.55+66041_55+66042delinsAT (n.55+66041_55+66042delinsAT)
n.559+66041_559+66042delinsAT
11g.99622311T>GCA2601727325CNTN5c.55+66042T>G (n.55+66042T>G)
n.559+66042T>G
dbSNP gnomAD v3 gnomAD v4
11g.99622313delCA1994941618CNTN5c.55+66044del (n.55+66044del)
n.559+66044del
dbSNP
11g.99622313T>ACA227975239CNTN5c.55+66044T>A (n.55+66044T>A)
n.559+66044T>A
dbSNP
11g.99622313T=CA1994941620CNTN5c.55+66044T= (n.55+66044T=)
n.559+66044T=
11g.99622315G>ACA227975240CNTN5c.55+66046G>A (n.55+66046G>A)
n.559+66046G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.99622315G=CA1994941623CNTN5c.55+66046G= (n.55+66046G=)
n.559+66046G=
11g.99622318T>GCA1994941627CNTN5c.55+66049T>G (n.55+66049T>G)
n.559+66049T>G
dbSNP
11g.99622318T=CA1994941625CNTN5c.55+66049T= (n.55+66049T=)
n.559+66049T=
11g.99622319A=CA1994941631CNTN5c.55+66050A= (n.55+66050A=)
n.559+66050A=
11g.99622319A>GCA227975241CNTN5c.55+66050A>G (n.55+66050A>G)
n.559+66050A>G
dbSNP

Number of alleles fetched