Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.68738212G>CCA623140005CDH1c.49-85G>C (p.=)
c.-1567-85G>C (p.=)
c.-1771-85G>C (p.=)
gnomAD
16g.68738222C>ACA283274121CDH1c.49-75C>A (p.=)
c.-1567-75C>A (p.=)
c.-1771-75C>A (p.=)
dbSNP gnomAD
16g.68738226G>ACA283274127CDH1c.49-71G>A (p.=)
c.-1567-71G>A (p.=)
c.-1771-71G>A (p.=)
dbSNP gnomAD
16g.68738243G>CCA914114360CDH1c.49-54G>C (p.=)
c.-1567-54G>C (p.=)
c.-1771-54G>C (p.=)
gnomAD
16g.68738245A>GCA496149581CDH1c.49-52A>G (p.=)
c.-1567-52A>G (p.=)
c.-1771-52A>G (p.=)
gnomAD
16g.68738245A>TCA283274147CDH1c.49-52A>T (p.=)
c.-1567-52A>T (p.=)
c.-1771-52A>T (p.=)
dbSNP
16g.68738246G>ACA623140006CDH1c.49-51G>A (p.=)
c.-1567-51G>A (p.=)
c.-1771-51G>A (p.=)
gnomAD
16g.68738250G>ACA623140007CDH1c.49-47G>A (p.=)
c.-1567-47G>A (p.=)
c.-1771-47G>A (p.=)
gnomAD
16g.68738251G>ACA8129788CDH1c.49-46G>A (p.=)
c.-1567-46G>A (p.=)
c.-1771-46G>A (p.=)
dbSNP ExAC gnomAD
16g.68738256C>TCA723157467CDH1c.49-41C>T (p.=)
c.-1567-41C>T (p.=)
c.-1771-41C>T (p.=)
16g.68738260G>TCA623140008CDH1c.49-37G>T (p.=)
c.-1567-37G>T (p.=)
c.-1771-37G>T (p.=)
gnomAD
16g.68738264C>TCA283274155CDH1c.49-33C>T (p.=)
c.-1567-33C>T (p.=)
c.-1771-33C>T (p.=)
dbSNP gnomAD
16g.68738265A>TCA723157472CDH1c.49-32A>T (p.=)
c.-1567-32A>T (p.=)
c.-1771-32A>T (p.=)
16g.68738266C>ACA723157473CDH1c.49-31C>A (p.=)
c.-1567-31C>A (p.=)
c.-1771-31C>A (p.=)
16g.68738268C>TCA623140009CDH1c.49-29C>T (p.=)
c.-1567-29C>T (p.=)
c.-1771-29C>T (p.=)
gnomAD
16g.68738273C>TCA623140010CDH1c.49-24C>T (p.=)
c.-1567-24C>T (p.=)
c.-1771-24C>T (p.=)
gnomAD
16g.68738277C>TCA8129789CDH1c.49-20C>T (p.=)
c.-1567-20C>T (p.=)
c.-1771-20C>T (p.=)
ClinVar dbSNP ExAC gnomAD
16g.68738278T>CCA658683943CDH1c.49-19T>C (p.=)
c.-1567-19T>C (p.=)
c.-1771-19T>C (p.=)
ClinVar
16g.68738279A>GCA723157484CDH1c.49-18A>G (p.=)
c.-1567-18A>G (p.=)
c.-1771-18A>G (p.=)
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
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 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.=)

Number of alleles fetched