Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.37966158_37966184delinsCGGCCAGTGGCCAGTCAGCGCCAAGGTCA1777329288ADRB3c.286_312delinsACCTTGGCGCTGACTGGCCACTGGCCG (p.Thr96=)
n.414_440delinsACCTTGGCGCTGACTGGCCACTGGCCG
8g.37966159_37966176delinsGGCCAGTGGCCAGTCAGCCA1777329291ADRB3c.294_311delinsGCTGACTGGCCACTGGCC (p.Ala98=)
n.422_439delinsGCTGACTGGCCACTGGCC
8g.37966163_37966188delCA175072285ADRB3c.286_311del (p.Thr96ValfsTer?)
n.414_439del
dbSNP gnomAD v4
8g.37966164_37966180delCA4714420ADRB3c.294_310del (p.Leu99ValfsTer?)
n.422_438del
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.37966169C>ACA370696263ADRB3c.301G>T (p.Gly101Cys)
n.429G>T
8g.37966169C=CA1777329297ADRB3c.301G= (p.Gly101=)
n.429G=
8g.37966169C>GCA370696268ADRB3c.301G>C (p.Gly101Arg)
n.429G>C
8g.37966169C>TCA370696275ADRB3c.301G>A (p.Gly101Ser)
n.429G>A
dbSNP gnomAD v2 gnomAD v4
8g.37966170A=CA1777329298ADRB3c.300T= (p.Thr100=)
n.428T=
8g.37966170A>CCA4714422ADRB3c.300T>G (p.Thr100=)
n.428T>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.37966170A>GCA460494698ADRB3c.300T>C (p.Thr100=)
n.428T>C
8g.37966170A>TCA460494699ADRB3c.300T>A (p.Thr100=)
n.428T>A
dbSNP gnomAD v2 gnomAD v4
8g.37966171G>ACA4714423ADRB3c.299C>T (p.Thr100Ile)
n.427C>T
dbSNP ExAC gnomAD v2 gnomAD v4
8g.37966171G>CCA370696286ADRB3c.299C>G (p.Thr100Ser)
n.427C>G
8g.37966171G=CA1777329299ADRB3c.299C= (p.Thr100=)
n.427C=
8g.37966171G>TCA370696287ADRB3c.299C>A (p.Thr100Asn)
n.427C>A
8g.37966172T>ACA370696298ADRB3c.298A>T (p.Thr100Ser)
n.426A>T
8g.37966172T>CCA175072320ADRB3c.298A>G (p.Thr100Ala)
n.426A>G
dbSNP
8g.37966172T>GCA370696293ADRB3c.298A>C (p.Thr100Pro)
n.426A>C
8g.37966172T=CA1777329300ADRB3c.298A= (p.Thr100=)
n.426A=
8g.37966173C>ACA460494703ADRB3c.297G>T (p.Leu99=)
n.425G>T
8g.37966173C>GCA460494706ADRB3c.297G>C (p.Leu99=)
n.425G>C
8g.37966173C>TCA460494705ADRB3c.297G>A (p.Leu99=)
n.425G>A
8g.37966174A>CCA370696302ADRB3c.296T>G (p.Leu99Arg)
n.424T>G
8g.37966174A>GCA370696303ADRB3c.296T>C (p.Leu99Pro)
n.424T>C
8g.37966174A>TCA370696304ADRB3c.296T>A (p.Leu99Gln)
n.424T>A
8g.37966175G>ACA460494707ADRB3c.295C>T (p.Leu99=)
n.423C>T
8g.37966175G>CCA370696305ADRB3c.295C>G (p.Leu99Val)
n.423C>G
8g.37966175G>TCA370696306ADRB3c.295C>A (p.Leu99Met)
n.423C>A
8g.37966176C>ACA460494708ADRB3c.294G>T (p.Ala98=)
n.422G>T
dbSNP gnomAD v2
8g.37966176C=CA1777329301ADRB3c.294G= (p.Ala98=)
n.422G=
8g.37966176C>GCA460494711ADRB3c.294G>C (p.Ala98=)
n.422G>C
8g.37966176C>TCA460494710ADRB3c.294G>A (p.Ala98=)
n.422G>A
dbSNP gnomAD v4
8g.37966177G>ACA175072327ADRB3c.293C>T (p.Ala98Val)
n.421C>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
8g.37966177G>CCA370696307ADRB3c.293C>G (p.Ala98Gly)
n.421C>G
8g.37966177G=CA1777329302ADRB3c.293C= (p.Ala98=)
n.421C=
8g.37966177G>TCA370696309ADRB3c.293C>A (p.Ala98Glu)
n.421C>A
8g.37966178C>ACA175072344ADRB3c.292G>T (p.Ala98Ser)
n.420G>T
dbSNP gnomAD v3 gnomAD v4
8g.37966178C=CA1777329303ADRB3c.292G= (p.Ala98=)
n.420G=
8g.37966178C>GCA370696314ADRB3c.292G>C (p.Ala98Pro)
n.420G>C
8g.37966178C>TCA370696315ADRB3c.292G>A (p.Ala98Thr)
n.420G>A
8g.37966179C>ACA370696317ADRB3c.291G>T (p.Leu97Phe)
n.419G>T
8g.37966179C>GCA370696321ADRB3c.291G>C (p.Leu97Phe)
n.419G>C
8g.37966179C>TCA460494719ADRB3c.291G>A (p.Leu97=)
n.419G>A
gnomAD v4
8g.37966180A>CCA370696336ADRB3c.290T>G (p.Leu97Trp)
n.418T>G
8g.37966180A>GCA370696331ADRB3c.290T>C (p.Leu97Ser)
n.418T>C
8g.37966180A>TCA370696326ADRB3c.290T>A (p.Leu97Ter)
n.418T>A
8g.37966181A=CA1777329304ADRB3c.289T= (p.Leu97=)
n.417T=
8g.37966181A>CCA370696876ADRB3c.289T>G (p.Leu97Val)
n.417T>G
8g.37966181A>GCA460494720ADRB3c.289T>C (p.Leu97=)
n.417T>C
gnomAD v4

Number of alleles fetched