Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.13854777C>ACA351623391WNT7Ac.325G>T (p.Ala109Ser)
c.124G>T (p.Ala42Ser)
3g.13854777C=CA1346837666WNT7Ac.325G= (p.Ala109=)
c.124G= (p.Ala42=)
3g.13854777C>GCA351623392WNT7Ac.325G>C (p.Ala109Pro)
c.124G>C (p.Ala42Pro)
3g.13854777C>TCA119262WNT7Ac.325G>A (p.Ala109Thr)
c.124G>A (p.Ala42Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.13854778G>ACA2266477WNT7Ac.324C>T (p.Tyr108=)
c.123C>T (p.Tyr41=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.13854778G>CCA351623393WNT7Ac.324C>G (p.Tyr108Ter)
c.123C>G (p.Tyr41Ter)
3g.13854778G=CA1346837673WNT7Ac.324C= (p.Tyr108=)
c.123C= (p.Tyr41=)
3g.13854778G>TCA351623394WNT7Ac.324C>A (p.Tyr108Ter)
c.123C>A (p.Tyr41Ter)
gnomAD v4
3g.13854779T>ACA351623395WNT7Ac.323A>T (p.Tyr108Phe)
c.122A>T (p.Tyr41Phe)
3g.13854779T>CCA351623396WNT7Ac.323A>G (p.Tyr108Cys)
c.122A>G (p.Tyr41Cys)
3g.13854779T>GCA351623397WNT7Ac.323A>C (p.Tyr108Ser)
c.122A>C (p.Tyr41Ser)
dbSNP
3g.13854779T=CA1346837676WNT7Ac.323A= (p.Tyr108=)
c.122A= (p.Tyr41=)
3g.13854780A>CCA351623398WNT7Ac.322T>G (p.Tyr108Asp)
c.121T>G (p.Tyr41Asp)
3g.13854780A>GCA351623399WNT7Ac.322T>C (p.Tyr108His)
c.121T>C (p.Tyr41His)
3g.13854780A>TCA351623400WNT7Ac.322T>A (p.Tyr108Asn)
c.121T>A (p.Tyr41Asn)
3g.13854781G>ACA2266478WNT7Ac.321C>T (p.Thr107=)
c.120C>T (p.Thr40=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.13854781G>CCA432695621WNT7Ac.321C>G (p.Thr107=)
c.120C>G (p.Thr40=)
3g.13854781G=CA1346837680WNT7Ac.321C= (p.Thr107=)
c.120C= (p.Thr40=)
3g.13854781G>TCA432695622WNT7Ac.321C>A (p.Thr107=)
c.120C>A (p.Thr40=)
3g.13854782G>ACA2266479WNT7Ac.320C>T (p.Thr107Ile)
c.119C>T (p.Thr40Ile)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.13854782G>CCA351623401WNT7Ac.320C>G (p.Thr107Ser)
c.119C>G (p.Thr40Ser)
3g.13854782G=CA1346837687WNT7Ac.320C= (p.Thr107=)
c.119C= (p.Thr40=)
3g.13854782G>TCA2266480WNT7Ac.320C>A (p.Thr107Asn)
c.119C>A (p.Thr40Asn)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.13854783T>ACA351623404WNT7Ac.319A>T (p.Thr107Ser)
c.118A>T (p.Thr40Ser)
3g.13854783T>CCA351623402WNT7Ac.319A>G (p.Thr107Ala)
c.118A>G (p.Thr40Ala)
3g.13854783T>GCA351623403WNT7Ac.319A>C (p.Thr107Pro)
c.118A>C (p.Thr40Pro)
dbSNP
3g.13854783T=CA1346837690WNT7Ac.319A= (p.Thr107=)
c.118A= (p.Thr40=)
3g.13854784G>ACA2266481WNT7Ac.318C>T (p.Phe106=)
c.117C>T (p.Phe39=)
dbSNP ExAC gnomAD v2
3g.13854784G>CCA351623405WNT7Ac.318C>G (p.Phe106Leu)
c.117C>G (p.Phe39Leu)
3g.13854784G=CA1346837694WNT7Ac.318C= (p.Phe106=)
c.117C= (p.Phe39=)
3g.13854784G>TCA351623406WNT7Ac.318C>A (p.Phe106Leu)
c.117C>A (p.Phe39Leu)
gnomAD v4
3g.13854785A=CA1346837698WNT7Ac.317T= (p.Phe106=)
c.116T= (p.Phe39=)
3g.13854785A>CCA351623407WNT7Ac.317T>G (p.Phe106Cys)
c.116T>G (p.Phe39Cys)
3g.13854785A>GCA351623408WNT7Ac.317T>C (p.Phe106Ser)
c.116T>C (p.Phe39Ser)
dbSNP
3g.13854785A>TCA351623409WNT7Ac.317T>A (p.Phe106Tyr)
c.116T>A (p.Phe39Tyr)
3g.13854785_13854786delCA2577516057WNT7Ac.316_317del (p.Phe106HisfsTer?)
c.115_116del (p.Phe39HisfsTer?)
3g.13854786A>CCA351623410WNT7Ac.316T>G (p.Phe106Val)
c.115T>G (p.Phe39Val)
gnomAD v4
3g.13854786A>GCA351623411WNT7Ac.316T>C (p.Phe106Leu)
c.115T>C (p.Phe39Leu)
3g.13854786A>TCA351623412WNT7Ac.316T>A (p.Phe106Ile)
c.115T>A (p.Phe39Ile)
3g.13854787C>ACA432695623WNT7Ac.315G>T (p.Ala105=)
c.114G>T (p.Ala38=)
gnomAD v4
3g.13854787C=CA1346837701WNT7Ac.315G= (p.Ala105=)
c.114G= (p.Ala38=)
3g.13854787C>GCA432695624WNT7Ac.315G>C (p.Ala105=)
c.114G>C (p.Ala38=)
3g.13854787C>TCA2266482WNT7Ac.315G>A (p.Ala105=)
c.114G>A (p.Ala38=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.13854788G>ACA2266483WNT7Ac.314C>T (p.Ala105Val)
c.113C>T (p.Ala38Val)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
3g.13854788G>CCA351623413WNT7Ac.314C>G (p.Ala105Gly)
c.113C>G (p.Ala38Gly)
gnomAD v4
3g.13854788G=CA1346837704WNT7Ac.314C= (p.Ala105=)
c.113C= (p.Ala38=)
3g.13854788G>TCA351623414WNT7Ac.314C>A (p.Ala105Glu)
c.113C>A (p.Ala38Glu)
COSMIC
3g.13854789C>ACA351623415WNT7Ac.313G>T (p.Ala105Ser)
c.112G>T (p.Ala38Ser)
3g.13854789C>GCA351623416WNT7Ac.313G>C (p.Ala105Pro)
c.112G>C (p.Ala38Pro)
3g.13854789C>TCA351623417WNT7Ac.313G>A (p.Ala105Thr)
c.112G>A (p.Ala38Thr)

Number of alleles fetched