Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.36461585G>ACA512325123CLDN14,CLDN14-AS1c.111C>T (p.Gly37=)
n.468+15578G>A
gnomAD v4
21g.36461585G>CCA512325121CLDN14,CLDN14-AS1c.111C>G (p.Gly37=)
n.468+15578G>C
21g.36461585G>TCA512325122CLDN14,CLDN14-AS1c.111C>A (p.Gly37=)
n.468+15578G>T
21g.36461586C>ACA409884456CLDN14,CLDN14-AS1c.110G>T (p.Gly37Val)
n.468+15579C>A
gnomAD v4
21g.36461586C>GCA409884464CLDN14,CLDN14-AS1c.110G>C (p.Gly37Ala)
n.468+15579C>G
21g.36461586C>TCA409884475CLDN14,CLDN14-AS1c.110G>A (p.Gly37Asp)
n.468+15579C>T
gnomAD v4
21g.36461587C>ACA409884488CLDN14,CLDN14-AS1c.109G>T (p.Gly37Cys)
n.468+15580C>A
21g.36461587C=CA2388017362CLDN14,CLDN14-AS1c.109G= (p.Gly37=)
n.468+15580C=
21g.36461587C>GCA409884490CLDN14,CLDN14-AS1c.109G>C (p.Gly37Arg)
n.468+15580C>G
21g.36461587C>TCA10019339CLDN14,CLDN14-AS1c.109G>A (p.Gly37Ser)
n.468+15580C>T
dbSNP ExAC gnomAD v2 gnomAD v4
21g.36461588C>ACA512325127CLDN14,CLDN14-AS1c.108G>T (p.Val36=)
n.468+15581C>A
21g.36461588C>GCA512325129CLDN14,CLDN14-AS1c.108G>C (p.Val36=)
n.468+15581C>G
21g.36461588C>TCA512325130CLDN14,CLDN14-AS1c.108G>A (p.Val36=)
n.468+15581C>T
21g.36461589A>CCA409884492CLDN14,CLDN14-AS1c.107T>G (p.Val36Gly)
n.468+15582A>C
21g.36461589A>GCA409884494CLDN14,CLDN14-AS1c.107T>C (p.Val36Ala)
n.468+15582A>G
21g.36461589A>TCA409884497CLDN14,CLDN14-AS1c.107T>A (p.Val36Glu)
n.468+15582A>T
21g.36461590C>ACA10019341CLDN14,CLDN14-AS1c.106G>T (p.Val36Leu)
n.468+15583C>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
21g.36461590C=CA2388017364CLDN14,CLDN14-AS1c.106G= (p.Val36=)
n.468+15583C=
21g.36461590C>GCA409884509CLDN14,CLDN14-AS1c.106G>C (p.Val36Leu)
n.468+15583C>G
gnomAD v4
21g.36461590C>TCA10019340CLDN14,CLDN14-AS1c.106G>A (p.Val36Met)
n.468+15583C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
21g.36461591G>ACA10019342CLDN14,CLDN14-AS1c.105C>T (p.His35=)
n.468+15584G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
21g.36461591G>CCA409884542CLDN14,CLDN14-AS1c.105C>G (p.His35Gln)
n.468+15584G>C
21g.36461591G=CA2388017367CLDN14,CLDN14-AS1c.105C= (p.His35=)
n.468+15584G=
21g.36461591G>TCA409884533CLDN14,CLDN14-AS1c.105C>A (p.His35Gln)
n.468+15584G>T
gnomAD v4
21g.36461592T>ACA409884543CLDN14,CLDN14-AS1c.104A>T (p.His35Leu)
n.468+15585T>A
21g.36461592T>CCA409884546CLDN14,CLDN14-AS1c.104A>G (p.His35Arg)
n.468+15585T>C
dbSNP
21g.36461592T>GCA409884544CLDN14,CLDN14-AS1c.104A>C (p.His35Pro)
n.468+15585T>G
21g.36461593G>ACA409884564CLDN14,CLDN14-AS1c.103C>T (p.His35Tyr)
n.468+15586G>A
21g.36461593G>CCA409884565CLDN14,CLDN14-AS1c.103C>G (p.His35Asp)
n.468+15586G>C
21g.36461593G>TCA409884567CLDN14,CLDN14-AS1c.103C>A (p.His35Asn)
n.468+15586G>T
gnomAD v4
21g.36461594C>ACA320314346CLDN14,CLDN14-AS1c.102G>T (p.Ala34=)
n.468+15587C>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
21g.36461594C=CA2388017369CLDN14,CLDN14-AS1c.102G= (p.Ala34=)
n.468+15587C=
21g.36461594C>GCA512324519CLDN14,CLDN14-AS1c.102G>C (p.Ala34=)
n.468+15587C>G
21g.36461594C>TCA10019343CLDN14,CLDN14-AS1c.102G>A (p.Ala34=)
n.468+15587C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
21g.36461595G>ACA409884581CLDN14,CLDN14-AS1c.101C>T (p.Ala34Val)
n.468+15588G>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
21g.36461595G>CCA409884584CLDN14,CLDN14-AS1c.101C>G (p.Ala34Gly)
n.468+15588G>C
21g.36461595G=CA2388017372CLDN14,CLDN14-AS1c.101C= (p.Ala34=)
n.468+15588G=
21g.36461595G>TCA10019344CLDN14,CLDN14-AS1c.101C>A (p.Ala34Glu)
n.468+15588G>T
dbSNP ExAC gnomAD v2 gnomAD v4
21g.36461596C>ACA409884593CLDN14,CLDN14-AS1c.100G>T (p.Ala34Ser)
n.468+15589C>A
21g.36461596C>GCA409884596CLDN14,CLDN14-AS1c.100G>C (p.Ala34Pro)
n.468+15589C>G
21g.36461596C>TCA409884597CLDN14,CLDN14-AS1c.100G>A (p.Ala34Thr)
n.468+15589C>T
21g.36461597T>ACA512324522CLDN14,CLDN14-AS1c.99A>T (p.Thr33=)
n.468+15590T>A
gnomAD v4
21g.36461597T>CCA320314377CLDN14,CLDN14-AS1c.99A>G (p.Thr33=)
n.468+15590T>C
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
21g.36461597T>GCA512324521CLDN14,CLDN14-AS1c.99A>C (p.Thr33=)
n.468+15590T>G
21g.36461597T=CA2388017374CLDN14,CLDN14-AS1c.99A= (p.Thr33=)
n.468+15590T=
21g.36461598G>ACA409884602CLDN14,CLDN14-AS1c.98C>T (p.Thr33Ile)
n.468+15591G>A
dbSNP
21g.36461598G>CCA409884608CLDN14,CLDN14-AS1c.98C>G (p.Thr33Arg)
n.468+15591G>C
21g.36461598G=CA2388017375CLDN14,CLDN14-AS1c.98C= (p.Thr33=)
n.468+15591G=
21g.36461598G>TCA409884614CLDN14,CLDN14-AS1c.98C>A (p.Thr33Lys)
n.468+15591G>T
21g.36461599T>ACA409884619CLDN14,CLDN14-AS1c.97A>T (p.Thr33Ser)
n.468+15592T>A

Number of alleles fetched