Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.68738299_68738413delCA645569984CDH1c.51_163+2del
c.-1565_-1453+2del
c.-1769_-1657+2del
ClinVar dbSNP 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.=)
16g.68738305T>CCA8129794CDH1c.57T>C (p.Ser19=)
c.-1559T>C (p.=)
c.-1763T>C (p.=)
dbSNP ExAC gnomAD
16g.68738305T>GCA496149587CDH1c.57T>G (p.Ser19=)
c.-1559T>G (p.=)
c.-1763T>G (p.=)
16g.68738306T>ACA396451624CDH1c.58T>A (p.Trp20Arg)
c.-1558T>A (p.=)
c.-1762T>A (p.=)
16g.68738306T>CCA396451627CDH1c.58T>C (p.Trp20Arg)
c.-1558T>C (p.=)
c.-1762T>C (p.=)
16g.68738306T>GCA396451628CDH1c.58T>G (p.Trp20Gly)
c.-1558T>G (p.=)
c.-1762T>G (p.=)
16g.68738307G>ACA280996CDH1c.59G>A (p.Trp20Ter)
c.-1557G>A (p.=)
c.-1761G>A (p.=)
ClinVar dbSNP COSMIC
16g.68738307G>CCA396451633CDH1c.59G>C (p.Trp20Ser)
c.-1557G>C (p.=)
c.-1761G>C (p.=)
ClinVar
16g.68738307G>TCA396451640CDH1c.59G>T (p.Trp20Leu)
c.-1557G>T (p.=)
c.-1761G>T (p.=)
16g.68738308G>ACA197127CDH1c.60G>A (p.Trp20Ter)
c.-1556G>A (p.=)
c.-1760G>A (p.=)
ClinVar dbSNP
16g.68738308G>CCA396451644CDH1c.60G>C (p.Trp20Cys)
c.-1556G>C (p.=)
c.-1760G>C (p.=)
16g.68738308G>TCA396451646CDH1c.60G>T (p.Trp20Cys)
c.-1556G>T (p.=)
c.-1760G>T (p.=)
16g.68738308_68738327delCA645569986CDH1c.60_79del (p.Trp20CysfsTer7)
c.-1556_-1537del (p.=)
c.-1760_-1741del (p.=)
COSMIC
16g.68738309C>ACA10577531CDH1c.61C>A (p.Leu21Ile)
c.-1555C>A (p.=)
c.-1759C>A (p.=)
ClinVar dbSNP
16g.68738309C>GCA10580066CDH1c.61C>G (p.Leu21Val)
c.-1555C>G (p.=)
c.-1759C>G (p.=)
ClinVar dbSNP gnomAD
16g.68738309C>TCA338485CDH1c.61C>T (p.Leu21Phe)
c.-1555C>T (p.=)
c.-1759C>T (p.=)
ClinVar dbSNP
16g.68738310T>ACA396451655CDH1c.62T>A (p.Leu21His)
c.-1554T>A (p.=)
c.-1758T>A (p.=)
16g.68738310T>CCA16620229CDH1c.62T>C (p.Leu21Pro)
c.-1554T>C (p.=)
c.-1758T>C (p.=)
ClinVar
16g.68738310T>GCA396451660CDH1c.62T>G (p.Leu21Arg)
c.-1554T>G (p.=)
c.-1758T>G (p.=)
16g.68738311C>ACA496149589CDH1c.63C>A (p.Leu21=)
c.-1553C>A (p.=)
c.-1757C>A (p.=)
16g.68738311C>GCA496149590CDH1c.63C>G (p.Leu21=)
c.-1553C>G (p.=)
c.-1757C>G (p.=)
16g.68738311C>TCA496149591CDH1c.63C>T (p.Leu21=)
c.-1553C>T (p.=)
c.-1757C>T (p.=)
ClinVar gnomAD
16g.68738312T>ACA396451663CDH1c.64T>A (p.Cys22Ser)
c.-1552T>A (p.=)
c.-1756T>A (p.=)
16g.68738312T>CCA396451667CDH1c.64T>C (p.Cys22Arg)
c.-1552T>C (p.=)
c.-1756T>C (p.=)
16g.68738312T>GCA396451670CDH1c.64T>G (p.Cys22Gly)
c.-1552T>G (p.=)
c.-1756T>G (p.=)
16g.68738313G>ACA396451671CDH1c.65G>A (p.Cys22Tyr)
c.-1551G>A (p.=)
c.-1755G>A (p.=)
ClinVar
16g.68738313G>CCA396451672CDH1c.65G>C (p.Cys22Ser)
c.-1551G>C (p.=)
c.-1755G>C (p.=)
16g.68738313G>TCA396451673CDH1c.65G>T (p.Cys22Phe)
c.-1551G>T (p.=)
c.-1755G>T (p.=)

Number of alleles fetched