Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.68738299_68738413delCA645569984CDH1c.51_163+2del
c.-1565_-1453+2del
c.-1769_-1657+2del
ClinVar COSMIC
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.=)
16g.68738314C>ACA283274268CDH1c.66C>A (p.Cys22Ter)
c.-1550C>A (p.=)
c.-1754C>A (p.=)
dbSNP
16g.68738314C>GCA396451679CDH1c.66C>G (p.Cys22Trp)
c.-1550C>G (p.=)
c.-1754C>G (p.=)
16g.68738314C>TCA10580067CDH1c.66C>T (p.Cys22=)
c.-1550C>T (p.=)
c.-1754C>T (p.=)
ClinVar dbSNP gnomAD
16g.68738315C>ACA396451682CDH1c.67C>A (p.Gln23Lys)
c.-1549C>A (p.=)
c.-1753C>A (p.=)
16g.68738315C>GCA396451688CDH1c.67C>G (p.Gln23Glu)
c.-1549C>G (p.=)
c.-1753C>G (p.=)
16g.68738315C>TCA396451685CDH1c.67C>T (p.Gln23Ter)
c.-1549C>T (p.=)
c.-1753C>T (p.=)
COSMIC
16g.68738316A>CCA396451696CDH1c.68A>C (p.Gln23Pro)
c.-1548A>C (p.=)
c.-1752A>C (p.=)
16g.68738316A>GCA396451698CDH1c.68A>G (p.Gln23Arg)
c.-1548A>G (p.=)
c.-1752A>G (p.=)
16g.68738316A>TCA396451702CDH1c.68A>T (p.Gln23Leu)
c.-1548A>T (p.=)
c.-1752A>T (p.=)
16g.68738317G>ACA193735CDH1c.69G>A (p.Gln23=)
c.-1547G>A (p.=)
c.-1751G>A (p.=)
ClinVar dbSNP
16g.68738317G>CCA396451707CDH1c.69G>C (p.Gln23His)
c.-1547G>C (p.=)
c.-1751G>C (p.=)
16g.68738317G>TCA396451710CDH1c.69G>T (p.Gln23His)
c.-1547G>T (p.=)
c.-1751G>T (p.=)
16g.68738318G>ACA396451711CDH1c.70G>A (p.Glu24Lys)
c.-1546G>A (p.=)
c.-1750G>A (p.=)
ClinVar
16g.68738318G>CCA396451713CDH1c.70G>C (p.Glu24Gln)
c.-1546G>C (p.=)
c.-1750G>C (p.=)
16g.68738318G>TCA280997CDH1c.70G>T (p.Glu24Ter)
c.-1546G>T (p.=)
c.-1750G>T (p.=)
ClinVar dbSNP
16g.68738319A>CCA396451719CDH1c.71A>C (p.Glu24Ala)
c.-1545A>C (p.=)
c.-1749A>C (p.=)
16g.68738319A>GCA396451721CDH1c.71A>G (p.Glu24Gly)
c.-1545A>G (p.=)
c.-1749A>G (p.=)
16g.68738319A>TCA396451724CDH1c.71A>T (p.Glu24Val)
c.-1545A>T (p.=)
c.-1749A>T (p.=)
16g.68738320G>ACA496149592CDH1c.72G>A (p.Glu24=)
c.-1544G>A (p.=)
c.-1748G>A (p.=)
16g.68738320G>CCA396451728CDH1c.72G>C (p.Glu24Asp)
c.-1544G>C (p.=)
c.-1748G>C (p.=)
16g.68738320G>TCA396451740CDH1c.72G>T (p.Glu24Asp)
c.-1544G>T (p.=)
c.-1748G>T (p.=)
16g.68738321C>ACA396451744CDH1c.73C>A (p.Pro25Thr)
c.-1543C>A (p.=)
c.-1747C>A (p.=)
16g.68738321C>GCA396451745CDH1c.73C>G (p.Pro25Ala)
c.-1543C>G (p.=)
c.-1747C>G (p.=)
16g.68738321C>TCA396451746CDH1c.73C>T (p.Pro25Ser)
c.-1543C>T (p.=)
c.-1747C>T (p.=)
16g.68738322C>ACA396451747CDH1c.74C>A (p.Pro25Gln)
c.-1542C>A (p.=)
c.-1746C>A (p.=)
16g.68738322C>GCA396451749CDH1c.74C>G (p.Pro25Arg)
c.-1542C>G (p.=)
c.-1746C>G (p.=)
16g.68738322C>TCA396451753CDH1c.74C>T (p.Pro25Leu)
c.-1542C>T (p.=)
c.-1746C>T (p.=)
ClinVar gnomAD
16g.68738323G>ACA192832CDH1c.75G>A (p.Pro25=)
c.-1541G>A (p.=)
c.-1745G>A (p.=)
ClinVar dbSNP COSMIC
16g.68738323G>CCA496149593CDH1c.75G>C (p.Pro25=)
c.-1541G>C (p.=)
c.-1745G>C (p.=)
16g.68738323G>TCA496149594CDH1c.75G>T (p.Pro25=)
c.-1541G>T (p.=)
c.-1745G>T (p.=)

Number of alleles fetched