Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.68738281C>GCA16042154CDH1c.49-16C>G (p.=)
c.-1567-16C>G (p.=)
c.-1771-16C>G (p.=)
ClinVar dbSNP gnomAD
16g.68738281C>TCA623140011CDH1c.49-16C>T (p.=)
c.-1567-16C>T (p.=)
c.-1771-16C>T (p.=)
ClinVar gnomAD
16g.68738282T>ACA16608220CDH1c.49-15T>A (p.=)
c.-1567-15T>A (p.=)
c.-1771-15T>A (p.=)
ClinVar
16g.68738282T>CCA8129790CDH1c.49-15T>C (p.=)
c.-1567-15T>C (p.=)
c.-1771-15T>C (p.=)
dbSNP ExAC gnomAD
16g.68738282T>GCA656476690CDH1c.49-15T>G (p.=)
c.-1567-15T>G (p.=)
c.-1771-15T>G (p.=)
COSMIC
16g.68738285C>TCA623140012CDH1c.49-12C>T (p.=)
c.-1567-12C>T (p.=)
c.-1771-12C>T (p.=)
gnomAD
16g.68738289dupCA396451536CDH1c.49-8dup (p.=)
c.-1567-8dup (p.=)
c.-1771-8dup (p.=)
ClinVar dbSNP
16g.68738286C>GCA8129791CDH1c.49-11C>G (p.=)
c.-1567-11C>G (p.=)
c.-1771-11C>G (p.=)
ClinVar dbSNP ExAC
16g.68738287C>TCA283274174CDH1c.49-10C>T (p.=)
c.-1567-10C>T (p.=)
c.-1771-10C>T (p.=)
ClinVar dbSNP
16g.68738288C>ACA658798616CDH1c.49-9C>A (p.=)
c.-1567-9C>A (p.=)
c.-1771-9C>A (p.=)
ClinVar
16g.68738289C>ACA8129792CDH1c.49-8C>A (p.=)
c.-1567-8C>A (p.=)
c.-1771-8C>A (p.=)
ClinVar dbSNP ExAC gnomAD
16g.68738289C>TCA16608223CDH1c.49-8C>T (p.=)
c.-1567-8C>T (p.=)
c.-1771-8C>T (p.=)
ClinVar dbSNP gnomAD
16g.68738290A>GCA16607045CDH1c.49-7A>G (p.=)
c.-1567-7A>G (p.=)
c.-1771-7A>G (p.=)
ClinVar
16g.68738291C>ACA623140013CDH1c.49-6C>A (p.=)
c.-1567-6C>A (p.=)
c.-1771-6C>A (p.=)
ClinVar gnomAD
16g.68738293C>ACA16607330CDH1c.49-4C>A (p.=)
c.-1567-4C>A (p.=)
c.-1771-4C>A (p.=)
ClinVar
16g.68738294C>ACA16620228CDH1c.49-3C>A (p.=)
c.-1567-3C>A (p.=)
c.-1771-3C>A (p.=)
ClinVar
16g.68738294C>TCA167975CDH1c.49-3C>T (p.=)
c.-1567-3C>T (p.=)
c.-1771-3C>T (p.=)
ClinVar dbSNP gnomAD
16g.68738295A>CCA396451549CDH1c.49-2A>C (p.=)
c.-1567-2A>C (p.=)
c.-1771-2A>C (p.=)
16g.68738295A>GCA16615353CDH1c.49-2A>G (p.=)
c.-1567-2A>G (p.=)
c.-1771-2A>G (p.=)
ClinVar
16g.68738295A>TCA396451551CDH1c.49-2A>T (p.=)
c.-1567-2A>T (p.=)
c.-1771-2A>T (p.=)
16g.68738299_68738413delCA645569984CDH1c.51_163+2del
c.-1565_-1453+2del
c.-1769_-1657+2del
ClinVar dbSNP COSMIC
16g.68738296G>ACA396451556CDH1c.49-1G>A (p.=)
c.-1567-1G>A (p.=)
c.-1771-1G>A (p.=)
16g.68738296G>CCA396451565CDH1c.49-1G>C (p.=)
c.-1567-1G>C (p.=)
c.-1771-1G>C (p.=)
16g.68738296G>TCA396451568CDH1c.49-1G>T (p.=)
c.-1567-1G>T (p.=)
c.-1771-1G>T (p.=)
16g.68738297G>ACA396451571CDH1c.49G>A (p.Val17Ile)
c.-1567G>A (p.=)
c.-1771G>A (p.=)
16g.68738297G>CCA16614951CDH1c.49G>C (p.Val17Leu)
c.-1567G>C (p.=)
c.-1771G>C (p.=)
ClinVar
16g.68738297G>TCA8129793CDH1c.49G>T (p.Val17Phe)
c.-1567G>T (p.=)
c.-1771G>T (p.=)
dbSNP ExAC gnomAD
16g.68738297_68738298insAGCA645569985CDH1c.49_50insAG (p.Val17GlufsTer?)
c.-1567_-1566insAG (p.=)
c.-1771_-1770insAG (p.=)
COSMIC
16g.68738298T>ACA396451578CDH1c.50T>A (p.Val17Asp)
c.-1566T>A (p.=)
c.-1770T>A (p.=)
16g.68738298T>CCA396451580CDH1c.50T>C (p.Val17Ala)
c.-1566T>C (p.=)
c.-1770T>C (p.=)
16g.68738298T>GCA396451582CDH1c.50T>G (p.Val17Gly)
c.-1566T>G (p.=)
c.-1770T>G (p.=)
16g.68738299C>ACA496149582CDH1c.51C>A (p.Val17=)
c.-1565C>A (p.=)
c.-1769C>A (p.=)
16g.68738299C>GCA496149583CDH1c.51C>G (p.Val17=)
c.-1565C>G (p.=)
c.-1769C>G (p.=)
16g.68738299C>TCA496149584CDH1c.51C>T (p.Val17=)
c.-1565C>T (p.=)
c.-1769C>T (p.=)
ClinVar
16g.68738300T>ACA396451586CDH1c.52T>A (p.Ser18Thr)
c.-1564T>A (p.=)
c.-1768T>A (p.=)
16g.68738300T>CCA396451589CDH1c.52T>C (p.Ser18Pro)
c.-1564T>C (p.=)
c.-1768T>C (p.=)
16g.68738300T>GCA396451593CDH1c.52T>G (p.Ser18Ala)
c.-1564T>G (p.=)
c.-1768T>G (p.=)
16g.68738301C>ACA396451600CDH1c.53C>A (p.Ser18Tyr)
c.-1563C>A (p.=)
c.-1767C>A (p.=)
16g.68738301C>GCA396451597CDH1c.53C>G (p.Ser18Cys)
c.-1563C>G (p.=)
c.-1767C>G (p.=)
16g.68738301C>TCA396451598CDH1c.53C>T (p.Ser18Phe)
c.-1563C>T (p.=)
c.-1767C>T (p.=)
16g.68738302C>ACA496149585CDH1c.54C>A (p.Ser18=)
c.-1562C>A (p.=)
c.-1766C>A (p.=)
16g.68738302C>GCA496149586CDH1c.54C>G (p.Ser18=)
c.-1562C>G (p.=)
c.-1766C>G (p.=)
16g.68738302C>TCA283274234CDH1c.54C>T (p.Ser18=)
c.-1562C>T (p.=)
c.-1766C>T (p.=)
dbSNP
16g.68738303T>ACA396451606CDH1c.55T>A (p.Ser19Thr)
c.-1561T>A (p.=)
c.-1765T>A (p.=)
16g.68738303T>CCA396451608CDH1c.55T>C (p.Ser19Pro)
c.-1561T>C (p.=)
c.-1765T>C (p.=)
16g.68738303T>GCA16614953CDH1c.55T>G (p.Ser19Ala)
c.-1561T>G (p.=)
c.-1765T>G (p.=)
ClinVar dbSNP gnomAD
16g.68738304C>ACA396451614CDH1c.56C>A (p.Ser19Tyr)
c.-1560C>A (p.=)
c.-1764C>A (p.=)
gnomAD
16g.68738304C>GCA396451616CDH1c.56C>G (p.Ser19Cys)
c.-1560C>G (p.=)
c.-1764C>G (p.=)
ClinVar
16g.68738304C>TCA396451618CDH1c.56C>T (p.Ser19Phe)
c.-1560C>T (p.=)
c.-1764C>T (p.=)
ClinVar gnomAD
16g.68738305T>ACA496149588CDH1c.57T>A (p.Ser19=)
c.-1559T>A (p.=)
c.-1763T>A (p.=)

Number of alleles fetched