Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.68737463G>ACA496149577CDH1c.48G>A (p.Gln16=)
c.-1568G>A (p.=)
c.-1772G>A (p.=)
ClinVar gnomAD
16g.68737463G>CCA396451427CDH1c.48G>C (p.Gln16His)
c.-1568G>C (p.=)
c.-1772G>C (p.=)
16g.68737463G=CA2229915345CDH1c.48G= (p.Gln16=)
c.-1568G= (p.=)
c.-1772G= (p.=)
16g.68737463G>TCA8129778CDH1c.48G>T (p.Gln16His)
c.-1568G>T (p.=)
c.-1772G>T (p.=)
ClinVar dbSNP ExAC gnomAD
16g.68737464G>ACA396451431CDH1c.48+1G>A (p.=)
c.-1568+1G>A (p.=)
c.-1772+1G>A (p.=)
ClinVar gnomAD
16g.68737464G>CCA396451434CDH1c.48+1G>C (p.=)
c.-1568+1G>C (p.=)
c.-1772+1G>C (p.=)
16g.68737464G=CA2229915352CDH1c.48+1G= (p.=)
c.-1568+1G= (p.=)
c.-1772+1G= (p.=)
16g.68737464G>TCA396451432CDH1c.48+1G>T (p.=)
c.-1568+1G>T (p.=)
c.-1772+1G>T (p.=)
gnomAD
16g.68737465T>ACA396451437CDH1c.48+2T>A (p.=)
c.-1568+2T>A (p.=)
c.-1772+2T>A (p.=)
16g.68737465T>CCA396451439CDH1c.48+2T>C (p.=)
c.-1568+2T>C (p.=)
c.-1772+2T>C (p.=)
16g.68737465T>GCA396451441CDH1c.48+2T>G (p.=)
c.-1568+2T>G (p.=)
c.-1772+2T>G (p.=)
16g.68737466A=CA2229915355CDH1c.48+3A= (p.=)
c.-1568+3A= (p.=)
c.-1772+3A= (p.=)
16g.68737466A>GCA8129779CDH1c.48+3A>G (p.=)
c.-1568+3A>G (p.=)
c.-1772+3A>G (p.=)
dbSNP ExAC gnomAD
16g.68737467C=CA2229915357CDH1c.48+4C= (p.=)
c.-1568+4C= (p.=)
c.-1772+4C= (p.=)
16g.68737467C>TCA8129780CDH1c.48+4C>T (p.=)
c.-1568+4C>T (p.=)
c.-1772+4C>T (p.=)
dbSNP ExAC
16g.68737468C>ACA283273547CDH1c.48+5C>A (p.=)
c.-1568+5C>A (p.=)
c.-1772+5C>A (p.=)
ClinVar dbSNP gnomAD
16g.68737468C=CA2229915370CDH1c.48+5C= (p.=)
c.-1568+5C= (p.=)
c.-1772+5C= (p.=)
16g.68737468C>GCA163551CDH1c.48+5C>G (p.=)
c.-1568+5C>G (p.=)
c.-1772+5C>G (p.=)
ClinVar dbSNP ExAC gnomAD
16g.68737468C>TCA8129781CDH1c.48+5C>T (p.=)
c.-1568+5C>T (p.=)
c.-1772+5C>T (p.=)
ClinVar dbSNP ExAC gnomAD
16g.68737468_68737469delinsATCA658683941CDH1c.48+5_48+6delinsAT (p.=)
c.-1568+5_-1568+6delinsAT (p.=)
c.-1772+5_-1772+6delinsAT (p.=)
ClinVar dbSNP
16g.68737468_68737469delinsCCCA2229915379CDH1c.48+5_48+6delinsCC (p.=)
c.-1568+5_-1568+6delinsCC (p.=)
c.-1772+5_-1772+6delinsCC (p.=)
16g.68737468_68737469delinsGTCA658683940CDH1c.48+5_48+6delinsGT (p.=)
c.-1568+5_-1568+6delinsGT (p.=)
c.-1772+5_-1772+6delinsGT (p.=)
ClinVar dbSNP
16g.68737468_68737469delinsTTCA658683939CDH1c.48+5_48+6delinsTT (p.=)
c.-1568+5_-1568+6delinsTT (p.=)
c.-1772+5_-1772+6delinsTT (p.=)
ClinVar dbSNP
16g.68737469C=CA2229915393CDH1c.48+6C= (p.=)
c.-1568+6C= (p.=)
c.-1772+6C= (p.=)
16g.68737469C>TCA200462CDH1c.48+6C>T (p.=)
c.-1568+6C>T (p.=)
c.-1772+6C>T (p.=)
ClinVar dbSNP ExAC gnomAD
16g.68737469_68737470delinsCCCA2229915389CDH1c.48+6_48+7delinsCC (p.=)
c.-1568+6_-1568+7delinsCC (p.=)
c.-1772+6_-1772+7delinsCC (p.=)
16g.68737469_68737470delinsTGCA913188714CDH1c.48+6_48+7delinsTG (p.=)
c.-1568+6_-1568+7delinsTG (p.=)
c.-1772+6_-1772+7delinsTG (p.=)
ClinVar dbSNP
16g.68737469_68737470delinsTTCA332838CDH1c.48+6_48+7delinsTT (p.=)
c.-1568+6_-1568+7delinsTT (p.=)
c.-1772+6_-1772+7delinsTT (p.=)
ClinVar dbSNP
16g.68737470C>ACA623139909CDH1c.48+7C>A (p.=)
c.-1568+7C>A (p.=)
c.-1772+7C>A (p.=)
gnomAD
16g.68737470C=CA2229915396CDH1c.48+7C= (p.=)
c.-1568+7C= (p.=)
c.-1772+7C= (p.=)
16g.68737470C>TCA168043CDH1c.48+7C>T (p.=)
c.-1568+7C>T (p.=)
c.-1772+7C>T (p.=)
ClinVar dbSNP ExAC gnomAD
16g.68737471G=CA2229915399CDH1c.48+8G= (p.=)
c.-1568+8G= (p.=)
c.-1772+8G= (p.=)
16g.68737471G>TCA623139911CDH1c.48+8G>T (p.=)
c.-1568+8G>T (p.=)
c.-1772+8G>T (p.=)
gnomAD
16g.68737473A=CA2229915401CDH1c.48+10A= (p.=)
c.-1568+10A= (p.=)
c.-1772+10A= (p.=)
16g.68737473A>GCA16608219CDH1c.48+10A>G (p.=)
c.-1568+10A>G (p.=)
c.-1772+10A>G (p.=)
ClinVar
16g.68737475C>ACA658683942CDH1c.48+12C>A (p.=)
c.-1568+12C>A (p.=)
c.-1772+12C>A (p.=)
ClinVar
16g.68737475C=CA2229915412CDH1c.48+12C= (p.=)
c.-1568+12C= (p.=)
c.-1772+12C= (p.=)
16g.68737475C>GCA913188715CDH1c.48+12C>G (p.=)
c.-1568+12C>G (p.=)
c.-1772+12C>G (p.=)
ClinVar
16g.68737475C>TCA623139912CDH1c.48+12C>T (p.=)
c.-1568+12C>T (p.=)
c.-1772+12C>T (p.=)
gnomAD
16g.68737476C>ACA623139913CDH1c.48+13C>A (p.=)
c.-1568+13C>A (p.=)
c.-1772+13C>A (p.=)
gnomAD
16g.68737476C=CA2229915419CDH1c.48+13C= (p.=)
c.-1568+13C= (p.=)
c.-1772+13C= (p.=)
16g.68737476C>TCA16607042CDH1c.48+13C>T (p.=)
c.-1568+13C>T (p.=)
c.-1772+13C>T (p.=)
ClinVar
16g.68737477C>ACA8129782CDH1c.48+14C>A (p.=)
c.-1568+14C>A (p.=)
c.-1772+14C>A (p.=)
dbSNP ExAC gnomAD
16g.68737477C=CA2229915425CDH1c.48+14C= (p.=)
c.-1568+14C= (p.=)
c.-1772+14C= (p.=)
16g.68737477C>TCA623139914CDH1c.48+14C>T (p.=)
c.-1568+14C>T (p.=)
c.-1772+14C>T (p.=)
gnomAD
16g.68737477_68737479delinsCCTCA2229915424CDH1c.48+14_48+16delinsCCT (p.=)
c.-1568+14_-1568+16delinsCCT (p.=)
c.-1772+14_-1772+16delinsCCT (p.=)
16g.68737478C>ACA623139917CDH1c.48+15C>A (p.=)
c.-1568+15C>A (p.=)
c.-1772+15C>A (p.=)
gnomAD
16g.68737478C=CA2229915430CDH1c.48+15C= (p.=)
c.-1568+15C= (p.=)
c.-1772+15C= (p.=)
16g.68737478C>TCA623139918CDH1c.48+15C>T (p.=)
c.-1568+15C>T (p.=)
c.-1772+15C>T (p.=)
gnomAD
16g.68737478_68737479delCA298944CDH1c.48+15_48+16del (p.=)
c.-1568+15_-1568+16del (p.=)
c.-1772+15_-1772+16del (p.=)
ClinVar dbSNP gnomAD

Number of alleles fetched