Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.68738294_68738409delinsCAGGTCTCCTCTTGGCTCTGCCAGGAGCCGGAGCCCTGCCACCCTGGCTTTGACGCCGAGAGCTACACGTTCACGGTGCCCCGGCGCCACCTGGAGAGAGGCCGCGTCCTGGGCAGCA2229916374CDH1c.49-3_161delinsCAGGTCTCCTCTTGGCTCTGCCAGGAGCCGGAGCCCTGCCACCCTGGCTTTGACGCCGAGAGCTACACGTTCACGGTGCCCCGGCGCCACCTGGAGAGAGGCCGCGTCCTGGGCAG
c.-1567-3_-1455delinsCAGGTCTCCTCTTGGCTCTGCCAGGAGCCGGAGCCCTGCCACCCTGGCTTTGACGCCGAGAGCTACACGTTCACGGTGCCCCGGCGCCACCTGGAGAGAGGCCGCGTCCTGGGCAG
c.-1771-3_-1659delinsCAGGTCTCCTCTTGGCTCTGCCAGGAGCCGGAGCCCTGCCACCCTGGCTTTGACGCCGAGAGCTACACGTTCACGGTGCCCCGGCGCCACCTGGAGAGAGGCCGCGTCCTGGGCAG
16g.68738299_68738413delCA645569984CDH1c.51_163+2del
c.-1565_-1453+2del
c.-1769_-1657+2del
ClinVar dbSNP COSMIC
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=CA2229916420CDH1c.59G= (p.Trp20=)
c.-1557G= (p.=)
c.-1761G= (p.=)
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=CA2229916429CDH1c.60G= (p.Trp20=)
c.-1556G= (p.=)
c.-1760G= (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=CA2229916444CDH1c.61C= (p.Leu21=)
c.-1555C= (p.=)
c.-1759C= (p.=)
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.68738310T=CA2229916448CDH1c.62T= (p.Leu21=)
c.-1554T= (p.=)
c.-1758T= (p.=)
16g.68738311C>ACA496149589CDH1c.63C>A (p.Leu21=)
c.-1553C>A (p.=)
c.-1757C>A (p.=)
16g.68738311C=CA2229916453CDH1c.63C= (p.Leu21=)
c.-1553C= (p.=)
c.-1757C= (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.68738312dupCA1139768322CDH1c.64dup (p.Cys22LeufsTer12)
c.-1552dup (p.=)
c.-1756dup (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=CA2229916456CDH1c.65G= (p.Cys22=)
c.-1551G= (p.=)
c.-1755G= (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=CA2229916461CDH1c.66C= (p.Cys22=)
c.-1550C= (p.=)
c.-1754C= (p.=)
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=CA2229916466CDH1c.67C= (p.Gln23=)
c.-1549C= (p.=)
c.-1753C= (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.=)
ClinVar COSMIC
16g.68738316A=CA2229916472CDH1c.68A= (p.Gln23=)
c.-1548A= (p.=)
c.-1752A= (p.=)
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.=)
ClinVar
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=CA2229916476CDH1c.69G= (p.Gln23=)
c.-1547G= (p.=)
c.-1751G= (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=CA2229916484CDH1c.70G= (p.Glu24=)
c.-1546G= (p.=)
c.-1750G= (p.=)

Number of alleles fetched