Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.36461453G>ACA133524CLDN14,CLDN14-AS1c.243C>T (p.Arg81=)
n.468+15446G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
21g.36461453G>CCA512324844CLDN14,CLDN14-AS1c.243C>G (p.Arg81=)
n.468+15446G>C
21g.36461453G=CA2388017217CLDN14,CLDN14-AS1c.243C= (p.Arg81=)
n.468+15446G=
21g.36461453G>TCA512324845CLDN14,CLDN14-AS1c.243C>A (p.Arg81=)
n.468+15446G>T
21g.36461453_36461454delinsATCA2740094709CLDN14,CLDN14-AS1c.242_243delinsAT (p.Arg81His)
n.468+15446_468+15447delinsAT
 ClinVar
21g.36461454C>ACA409882581CLDN14,CLDN14-AS1c.242G>T (p.Arg81Leu)
n.468+15447C>A
 dbSNP gnomAD v2
21g.36461454C=CA2388017218CLDN14,CLDN14-AS1c.242G= (p.Arg81=)
n.468+15447C=
21g.36461454C>GCA409882580CLDN14,CLDN14-AS1c.242G>C (p.Arg81Pro)
n.468+15447C>G
21g.36461454C>TCA199222CLDN14,CLDN14-AS1c.242G>A (p.Arg81His)
n.468+15447C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
21g.36461455G>ACA10019312CLDN14,CLDN14-AS1c.241C>T (p.Arg81Cys)
n.468+15448G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
21g.36461455G>CCA409882596CLDN14,CLDN14-AS1c.241C>G (p.Arg81Gly)
n.468+15448G>C
21g.36461455G=CA2388017219CLDN14,CLDN14-AS1c.241C= (p.Arg81=)
n.468+15448G=
21g.36461455G>TCA409882599CLDN14,CLDN14-AS1c.241C>A (p.Arg81Ser)
n.468+15448G>T
 gnomAD v4
21g.36461456G>ACA512324848CLDN14,CLDN14-AS1c.240C>T (p.Ala80=)
n.468+15449G>A
21g.36461456G>CCA512324849CLDN14,CLDN14-AS1c.240C>G (p.Ala80=)
n.468+15449G>C
21g.36461456G>TCA512324850CLDN14,CLDN14-AS1c.240C>A (p.Ala80=)
n.468+15449G>T
21g.36461457G>ACA10019313CLDN14,CLDN14-AS1c.239C>T (p.Ala80Val)
n.468+15450G>A
 dbSNP ExAC gnomAD v2 gnomAD v4
21g.36461457G>CCA409882609CLDN14,CLDN14-AS1c.239C>G (p.Ala80Gly)
n.468+15450G>C
21g.36461457G=CA2388017220CLDN14,CLDN14-AS1c.239C= (p.Ala80=)
n.468+15450G=
21g.36461457G>TCA409882610CLDN14,CLDN14-AS1c.239C>A (p.Ala80Asp)
n.468+15450G>T
21g.36461458C>ACA409882612CLDN14,CLDN14-AS1c.238G>T (p.Ala80Ser)
n.468+15451C>A
 gnomAD v4
21g.36461458C>GCA409882619CLDN14,CLDN14-AS1c.238G>C (p.Ala80Pro)
n.468+15451C>G
21g.36461458C>TCA409882621CLDN14,CLDN14-AS1c.238G>A (p.Ala80Thr)
n.468+15451C>T
21g.36461459A>CCA512324854CLDN14,CLDN14-AS1c.237T>G (p.Ala79=)
n.468+15452A>C
21g.36461459A>GCA512324855CLDN14,CLDN14-AS1c.237T>C (p.Ala79=)
n.468+15452A>G
 gnomAD v4
21g.36461459A>TCA512324857CLDN14,CLDN14-AS1c.237T>A (p.Ala79=)
n.468+15452A>T
21g.36461460G>ACA409882628CLDN14,CLDN14-AS1c.236C>T (p.Ala79Val)
n.468+15453G>A
21g.36461460G>CCA409882633CLDN14,CLDN14-AS1c.236C>G (p.Ala79Gly)
n.468+15453G>C
21g.36461460G>TCA409882635CLDN14,CLDN14-AS1c.236C>A (p.Ala79Asp)
n.468+15453G>T
 gnomAD v4
21g.36461461C>ACA409882667CLDN14,CLDN14-AS1c.235G>T (p.Ala79Ser)
n.468+15454C>A
21g.36461461C>GCA409882648CLDN14,CLDN14-AS1c.235G>C (p.Ala79Pro)
n.468+15454C>G
21g.36461461C>TCA409882656CLDN14,CLDN14-AS1c.235G>A (p.Ala79Thr)
n.468+15454C>T
 gnomAD v4
21g.36461462C>ACA409882670CLDN14,CLDN14-AS1c.234G>T (p.Gln78His)
n.468+15455C>A
21g.36461462C=CA2388017221CLDN14,CLDN14-AS1c.234G= (p.Gln78=)
n.468+15455C=
21g.36461462C>GCA10019314CLDN14,CLDN14-AS1c.234G>C (p.Gln78His)
n.468+15455C>G
 dbSNP ExAC gnomAD v2 gnomAD v4
21g.36461462C>TCA512324862CLDN14,CLDN14-AS1c.234G>A (p.Gln78=)
n.468+15455C>T
21g.36461463T>ACA409882675CLDN14,CLDN14-AS1c.233A>T (p.Gln78Leu)
n.468+15456T>A
21g.36461463T>CCA409882676CLDN14,CLDN14-AS1c.233A>G (p.Gln78Arg)
n.468+15456T>C
21g.36461463T>GCA409882677CLDN14,CLDN14-AS1c.233A>C (p.Gln78Pro)
n.468+15456T>G
21g.36461464G>ACA320314177CLDN14,CLDN14-AS1c.232C>T (p.Gln78Ter)
n.468+15457G>A
 dbSNP gnomAD v4
21g.36461464G>CCA409882683CLDN14,CLDN14-AS1c.232C>G (p.Gln78Glu)
n.468+15457G>C
21g.36461464G=CA2388017222CLDN14,CLDN14-AS1c.232C= (p.Gln78=)
n.468+15457G=
21g.36461464G>TCA409882684CLDN14,CLDN14-AS1c.232C>A (p.Gln78Lys)
n.468+15457G>T
21g.36461465G>ACA512324866CLDN14,CLDN14-AS1c.231C>T (p.Leu77=)
n.468+15458G>A
 dbSNP gnomAD v2 gnomAD v4
21g.36461465G>CCA512324864CLDN14,CLDN14-AS1c.231C>G (p.Leu77=)
n.468+15458G>C
21g.36461465G=CA2388017223CLDN14,CLDN14-AS1c.231C= (p.Leu77=)
n.468+15458G=
21g.36461465G>TCA512324865CLDN14,CLDN14-AS1c.231C>A (p.Leu77=)
n.468+15458G>T
21g.36461466A>CCA409882689CLDN14,CLDN14-AS1c.230T>G (p.Leu77Arg)
n.468+15459A>C
21g.36461466A>GCA409882694CLDN14,CLDN14-AS1c.230T>C (p.Leu77Pro)
n.468+15459A>G
21g.36461466A>TCA409882698CLDN14,CLDN14-AS1c.230T>A (p.Leu77His)
n.468+15459A>T

Number of alleles fetched