Chr Mutation (hg38) CAid Gene Transcript Linkouts
22g.50626202C>ACA412174553ARSAc.931G>T (p.Gly311Cys)
c.673G>T (p.Gly225Cys)
gnomAD
22g.50626202C>GCA412174550ARSAc.931G>C (p.Gly311Arg)
c.673G>C (p.Gly225Arg)
22g.50626202C>TCA115967ARSAc.931G>A (p.Gly311Ser)
c.673G>A (p.Gly225Ser)
ClinVar dbSNP ExAC gnomAD
22g.50626203G>ACA10324871ARSAc.930C>T (p.Gly310=)
c.672C>T (p.Gly224=)
ClinVar dbSNP ExAC gnomAD COSMIC
22g.50626203G>CCA515248966ARSAc.930C>G (p.Gly310=)
c.672C>G (p.Gly224=)
22g.50626203G>TCA515248967ARSAc.930C>A (p.Gly310=)
c.672C>A (p.Gly224=)
COSMIC
22g.50626204C>ACA219084ARSAc.929G>T (p.Gly310Val)
c.671G>T (p.Gly224Val)
ClinVar dbSNP
22g.50626204C>GCA412174557ARSAc.929G>C (p.Gly310Ala)
c.671G>C (p.Gly224Ala)
22g.50626204C>TCA219082ARSAc.929G>A (p.Gly310Asp)
c.671G>A (p.Gly224Asp)
ClinVar dbSNP
22g.50626204delCA16042037ARSAc.927del (p.Gly310AlafsTer19)
c.669del (p.Gly224AlafsTer19)
ClinVar dbSNP
22g.50626205C>ACA412174562ARSAc.928G>T (p.Gly310Cys)
c.670G>T (p.Gly224Cys)
22g.50626205C>GCA412174566ARSAc.928G>C (p.Gly310Arg)
c.670G>C (p.Gly224Arg)
22g.50626205C>TCA412174565ARSAc.928G>A (p.Gly310Ser)
c.670G>A (p.Gly224Ser)
22g.50626206C>ACA412174569ARSAc.927G>T (p.Glu309Asp)
c.669G>T (p.Glu223Asp)
22g.50626206C>GCA412174572ARSAc.927G>C (p.Glu309Asp)
c.669G>C (p.Glu223Asp)
22g.50626206C>TCA10324872ARSAc.927G>A (p.Glu309=)
c.669G>A (p.Glu223=)
dbSNP ExAC gnomAD
22g.50626207T>ACA412174579ARSAc.926A>T (p.Glu309Val)
c.668A>T (p.Glu223Val)
ClinVar
22g.50626207T>CCA412174585ARSAc.926A>G (p.Glu309Gly)
c.668A>G (p.Glu223Gly)
22g.50626207T>GCA412174589ARSAc.926A>C (p.Glu309Ala)
c.668A>C (p.Glu223Ala)
22g.50626207dupCA913088704ARSAc.926dup (p.Gly311ArgfsTer?)
c.668dup (p.Gly225ArgfsTer?)
22g.50626208C>ACA10324873ARSAc.925G>T (p.Glu309Ter)
c.667G>T (p.Glu223Ter)
dbSNP ExAC gnomAD
22g.50626208C>GCA10324874ARSAc.925G>C (p.Glu309Gln)
c.667G>C (p.Glu223Gln)
dbSNP ExAC gnomAD
22g.50626208C>TCA219080ARSAc.925G>A (p.Glu309Lys)
c.667G>A (p.Glu223Lys)
ClinVar dbSNP gnomAD
22g.50626208dupCA658824685ARSAc.925dup (p.Glu309GlyfsTer?)
c.667dup (p.Glu223GlyfsTer?)
ClinVar dbSNP
22g.50626209G>ACA10324875ARSAc.924C>T (p.Tyr308=)
c.666C>T (p.Tyr222=)
dbSNP ExAC gnomAD COSMIC
22g.50626209G>CCA412174606ARSAc.924C>G (p.Tyr308Ter)
c.666C>G (p.Tyr222Ter)
22g.50626209G>TCA412174610ARSAc.924C>A (p.Tyr308Ter)
c.666C>A (p.Tyr222Ter)
22g.50626210T>ACA412174621ARSAc.923A>T (p.Tyr308Phe)
c.665A>T (p.Tyr222Phe)
22g.50626210T>CCA412174619ARSAc.923A>G (p.Tyr308Cys)
c.665A>G (p.Tyr222Cys)
22g.50626210T>GCA412174615ARSAc.923A>C (p.Tyr308Ser)
c.665A>C (p.Tyr222Ser)
22g.50626211A>CCA412174627ARSAc.922T>G (p.Tyr308Asp)
c.664T>G (p.Tyr222Asp)
22g.50626211A>GCA219078ARSAc.922T>C (p.Tyr308His)
c.664T>C (p.Tyr222His)
ClinVar dbSNP
22g.50626211A>TCA412174625ARSAc.922T>A (p.Tyr308Asn)
c.664T>A (p.Tyr222Asn)
22g.50626212G>ACA515248968ARSAc.921C>T (p.Thr307=)
c.663C>T (p.Thr221=)
22g.50626212G>CCA515248969ARSAc.921C>G (p.Thr307=)
c.663C>G (p.Thr221=)
22g.50626212G>TCA515248970ARSAc.921C>A (p.Thr307=)
c.663C>A (p.Thr221=)
22g.50626213G>ACA412174630ARSAc.920C>T (p.Thr307Ile)
c.662C>T (p.Thr221Ile)
22g.50626213G>CCA412174632ARSAc.920C>G (p.Thr307Ser)
c.662C>G (p.Thr221Ser)
22g.50626213G>TCA10324876ARSAc.920C>A (p.Thr307Asn)
c.662C>A (p.Thr221Asn)
dbSNP ExAC gnomAD
22g.50626214T>ACA412174637ARSAc.919A>T (p.Thr307Ser)
c.661A>T (p.Thr221Ser)
22g.50626214T>CCA412174638ARSAc.919A>G (p.Thr307Ala)
c.661A>G (p.Thr221Ala)
22g.50626214T>GCA412174640ARSAc.919A>C (p.Thr307Pro)
c.661A>C (p.Thr221Pro)
22g.50626215C>ACA515248971ARSAc.918G>T (p.Thr306=)
c.660G>T (p.Thr220=)
22g.50626215C>GCA10324878ARSAc.918G>C (p.Thr306=)
c.660G>C (p.Thr220=)
dbSNP ExAC gnomAD
22g.50626215C>TCA10324877ARSAc.918G>A (p.Thr306=)
c.660G>A (p.Thr220=)
ClinVar dbSNP ExAC gnomAD
22g.50626216G>ACA219074ARSAc.917C>T (p.Thr306Met)
c.659C>T (p.Thr220Met)
ClinVar dbSNP
22g.50626216G>CCA412174662ARSAc.917C>G (p.Thr306Arg)
c.659C>G (p.Thr220Arg)
22g.50626216G>TCA412174665ARSAc.917C>A (p.Thr306Lys)
c.659C>A (p.Thr220Lys)
22g.50626217T>ACA412174668ARSAc.916A>T (p.Thr306Ser)
c.658A>T (p.Thr220Ser)
22g.50626217T>CCA412174667ARSAc.916A>G (p.Thr306Ala)
c.658A>G (p.Thr220Ala)

Number of alleles fetched