Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.37965892_37965900delCA2544682167ADRB3c.570_578del (p.His190_Pro193delinsGln)
n.698_706del
c.54_62del (p.His18_Pro21delinsGln)
8g.37965896T>ACA370694814ADRB3c.574A>T (p.Asn192Tyr)
n.702A>T
c.58A>T (p.Asn20Tyr)
8g.37965896T>CCA370694816ADRB3c.574A>G (p.Asn192Asp)
n.702A>G
c.58A>G (p.Asn20Asp)
8g.37965896T>GCA370694815ADRB3c.574A>C (p.Asn192His)
n.702A>C
c.58A>C (p.Asn20His)
8g.37965897G>ACA460495107ADRB3c.573C>T (p.Ser191=)
n.701C>T
c.57C>T (p.Ser19=)
dbSNP gnomAD v2
8g.37965897G>CCA460495108ADRB3c.573C>G (p.Ser191=)
n.701C>G
c.57C>G (p.Ser19=)
8g.37965897G=CA1777329143ADRB3c.573C= (p.Ser191=)
n.701C=
c.57C= (p.Ser19=)
8g.37965897G>TCA460495109ADRB3c.573C>A (p.Ser191=)
n.701C>A
c.57C>A (p.Ser19=)
8g.37965898G>ACA370694817ADRB3c.572C>T (p.Ser191Phe)
n.700C>T
c.56C>T (p.Ser19Phe)
8g.37965898G>CCA370694820ADRB3c.572C>G (p.Ser191Cys)
n.700C>G
c.56C>G (p.Ser19Cys)
8g.37965898G>TCA370694825ADRB3c.572C>A (p.Ser191Tyr)
n.700C>A
c.56C>A (p.Ser19Tyr)
8g.37965899A>CCA370694826ADRB3c.571T>G (p.Ser191Ala)
n.699T>G
c.55T>G (p.Ser19Ala)
8g.37965899A>GCA370694827ADRB3c.571T>C (p.Ser191Pro)
n.699T>C
c.55T>C (p.Ser19Pro)
8g.37965899A>TCA370694835ADRB3c.571T>A (p.Ser191Thr)
n.699T>A
c.55T>A (p.Ser19Thr)
8g.37965900G>ACA460495111ADRB3c.570C>T (p.His190=)
n.698C>T
c.54C>T (p.His18=)
dbSNP gnomAD v2 gnomAD v4
8g.37965900G>CCA4714379ADRB3c.570C>G (p.His190Gln)
n.698C>G
c.54C>G (p.His18Gln)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.37965900G=CA1777329144ADRB3c.570C= (p.His190=)
n.698C=
c.54C= (p.His18=)
8g.37965900G>TCA370694838ADRB3c.570C>A (p.His190Gln)
n.698C>A
c.54C>A (p.His18Gln)
8g.37965901T>ACA370694841ADRB3c.569A>T (p.His190Leu)
n.697A>T
c.53A>T (p.His18Leu)
gnomAD v4
8g.37965901T>CCA370694845ADRB3c.569A>G (p.His190Arg)
n.697A>G
c.53A>G (p.His18Arg)
dbSNP gnomAD v3 gnomAD v4
8g.37965901T>GCA370694849ADRB3c.569A>C (p.His190Pro)
n.697A>C
c.53A>C (p.His18Pro)
dbSNP
8g.37965901T=CA1777329145ADRB3c.569A= (p.His190=)
n.697A=
c.53A= (p.His18=)
8g.37965902G>ACA370694852ADRB3c.568C>T (p.His190Tyr)
n.696C>T
c.52C>T (p.His18Tyr)
8g.37965902G>CCA370694857ADRB3c.568C>G (p.His190Asp)
n.696C>G
c.52C>G (p.His18Asp)
8g.37965902G>TCA370694855ADRB3c.568C>A (p.His190Asn)
n.696C>A
c.52C>A (p.His18Asn)
8g.37965902_37965903insTACA2686921906ADRB3c.567_568insTA (p.His190TyrfsTer?)
n.695_696insTA
c.51_52insTA (p.His18TyrfsTer?)
gnomAD v4
8g.37965903G>ACA460495114ADRB3c.567C>T (p.Cys189=)
n.695C>T
c.51C>T (p.Cys17=)
8g.37965903G>CCA370694860ADRB3c.567C>G (p.Cys189Trp)
n.695C>G
c.51C>G (p.Cys17Trp)
gnomAD v4
8g.37965903G>TCA370694861ADRB3c.567C>A (p.Cys189Ter)
n.695C>A
c.51C>A (p.Cys17Ter)
gnomAD v4
8g.37965904delCA2686921907ADRB3c.566del (p.Cys189SerfsTer?)
n.694del
c.50del (p.Cys17SerfsTer?)
gnomAD v4
8g.37965904C>ACA370694864ADRB3c.566G>T (p.Cys189Phe)
n.694G>T
c.50G>T (p.Cys17Phe)
8g.37965904C>GCA370694865ADRB3c.566G>C (p.Cys189Ser)
n.694G>C
c.50G>C (p.Cys17Ser)
8g.37965904C>TCA370694867ADRB3c.566G>A (p.Cys189Tyr)
n.694G>A
c.50G>A (p.Cys17Tyr)
gnomAD v4
8g.37965904_37965909delCA2686921908ADRB3c.561_566del (p.Gln187_Cys189delinsHis)
n.689_694del
c.45_50del (p.Gln15_Cys17delinsHis)
gnomAD v4
8g.37965905A>CCA370694869ADRB3c.565T>G (p.Cys189Gly)
n.693T>G
c.49T>G (p.Cys17Gly)
8g.37965905A>GCA370694872ADRB3c.565T>C (p.Cys189Arg)
n.693T>C
c.49T>C (p.Cys17Arg)
8g.37965905A>TCA370694874ADRB3c.565T>A (p.Cys189Ser)
n.693T>A
c.49T>A (p.Cys17Ser)
8g.37965905_37965906insAGGGCA645566955ADRB3c.564_565insCCCT (p.Cys189ProfsTer?)
n.692_693insCCCT
c.48_49insCCCT (p.Cys17ProfsTer?)
COSMIC
8g.37965905_37965906insCTCCAACCCCA2553781638ADRB3c.564_565insGGGTTGGAG (p.Arg188_Cys189insGlyLeuGlu)
n.692_693insGGGTTGGAG
c.48_49insGGGTTGGAG (p.Arg16_Cys17insGlyLeuGlu)
8g.37965906G>ACA460495119ADRB3c.564C>T (p.Arg188=)
n.692C>T
c.48C>T (p.Arg16=)
gnomAD v4
8g.37965906G>CCA460495120ADRB3c.564C>G (p.Arg188=)
n.692C>G
c.48C>G (p.Arg16=)
8g.37965906G>TCA460495121ADRB3c.564C>A (p.Arg188=)
n.692C>A
c.48C>A (p.Arg16=)
8g.37965906_37965909delCA2686921909ADRB3c.561_564del (p.Gln187HisfsTer?)
n.689_692del
c.45_48del (p.Gln15HisfsTer?)
gnomAD v4
8g.37965907C>ACA370694876ADRB3c.563G>T (p.Arg188Leu)
n.691G>T
c.47G>T (p.Arg16Leu)
dbSNP gnomAD v2 gnomAD v4
8g.37965907C=CA1777329146ADRB3c.563G= (p.Arg188=)
n.691G=
c.47G= (p.Arg16=)
8g.37965907C>GCA175071756ADRB3c.563G>C (p.Arg188Pro)
n.691G>C
c.47G>C (p.Arg16Pro)
dbSNP gnomAD v4
8g.37965907C>TCA370694879ADRB3c.563G>A (p.Arg188His)
n.691G>A
c.47G>A (p.Arg16His)
gnomAD v4
8g.37965908G>ACA370694887ADRB3c.562C>T (p.Arg188Cys)
n.690C>T
c.46C>T (p.Arg16Cys)
gnomAD v4
8g.37965908G>CCA370694885ADRB3c.562C>G (p.Arg188Gly)
n.690C>G
c.46C>G (p.Arg16Gly)
gnomAD v4
8g.37965908G=CA1777329147ADRB3c.562C= (p.Arg188=)
n.690C=
c.46C= (p.Arg16=)

Number of alleles fetched