Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.37966094C>ACA370695687ADRB3c.376G>T (p.Glu126Ter)
n.504G>T
8g.37966094C=CA1777329261ADRB3c.376G= (p.Glu126=)
n.504G=
8g.37966094C>GCA370695689ADRB3c.376G>C (p.Glu126Gln)
n.504G>C
dbSNP gnomAD v2
8g.37966094C>TCA4714410ADRB3c.376G>A (p.Glu126Lys)
n.504G>A
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
8g.37966095G>ACA460494552ADRB3c.375C>T (p.Ile125=)
n.503C>T
8g.37966095G>CCA370695693ADRB3c.375C>G (p.Ile125Met)
n.503C>G
dbSNP gnomAD v4
8g.37966095G=CA1777329262ADRB3c.375C= (p.Ile125=)
n.503C=
8g.37966095G>TCA460494553ADRB3c.375C>A (p.Ile125=)
n.503C>A
8g.37966096A=CA1777329263ADRB3c.374T= (p.Ile125=)
n.502T=
8g.37966096A>CCA370695694ADRB3c.374T>G (p.Ile125Ser)
n.502T>G
8g.37966096A>GCA4714411ADRB3c.374T>C (p.Ile125Thr)
n.502T>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.37966096A>TCA370695697ADRB3c.374T>A (p.Ile125Asn)
n.502T>A
8g.37966097T>ACA370695700ADRB3c.373A>T (p.Ile125Phe)
n.501A>T
8g.37966097T>CCA370695703ADRB3c.373A>G (p.Ile125Val)
n.501A>G
8g.37966097T>GCA370695707ADRB3c.373A>C (p.Ile125Leu)
n.501A>C
8g.37966098G>ACA460494556ADRB3c.372C>T (p.Ser124=)
n.500C>T
8g.37966098G>CCA370695709ADRB3c.372C>G (p.Ser124Arg)
n.500C>G
8g.37966098G>TCA370695711ADRB3c.372C>A (p.Ser124Arg)
n.500C>A
8g.37966099C>ACA370695713ADRB3c.371G>T (p.Ser124Ile)
n.499G>T
8g.37966099C>GCA370695716ADRB3c.371G>C (p.Ser124Thr)
n.499G>C
8g.37966099C>TCA370695718ADRB3c.371G>A (p.Ser124Asn)
n.499G>A
8g.37966100T>ACA370695720ADRB3c.370A>T (p.Ser124Cys)
n.498A>T
8g.37966100T>CCA370695723ADRB3c.370A>G (p.Ser124Gly)
n.498A>G
8g.37966100T>GCA370695726ADRB3c.370A>C (p.Ser124Arg)
n.498A>C
8g.37966101G>ACA460494559ADRB3c.369C>T (p.Ala123=)
n.497C>T
8g.37966101G>CCA460494561ADRB3c.369C>G (p.Ala123=)
n.497C>G
8g.37966101G>TCA460494562ADRB3c.369C>A (p.Ala123=)
n.497C>A
gnomAD v4
8g.37966102G>ACA370695728ADRB3c.368C>T (p.Ala123Val)
n.496C>T
8g.37966102G>CCA370695729ADRB3c.368C>G (p.Ala123Gly)
n.496C>G
8g.37966102G>TCA370695732ADRB3c.368C>A (p.Ala123Asp)
n.496C>A
8g.37966103C>ACA370695735ADRB3c.367G>T (p.Ala123Ser)
n.495G>T
gnomAD v4
8g.37966103C=CA1777329264ADRB3c.367G= (p.Ala123=)
n.495G=
8g.37966103C>GCA370695738ADRB3c.367G>C (p.Ala123Pro)
n.495G>C
8g.37966103C>TCA175072217ADRB3c.367G>A (p.Ala123Thr)
n.495G>A
dbSNP gnomAD v4
8g.37966104G>ACA460494563ADRB3c.366C>T (p.Thr122=)
n.494C>T
COSMIC
8g.37966104G>CCA460494564ADRB3c.366C>G (p.Thr122=)
n.494C>G
gnomAD v4
8g.37966104G=CA1777329265ADRB3c.366C= (p.Thr122=)
n.494C=
8g.37966104G>TCA4714412ADRB3c.366C>A (p.Thr122=)
n.494C>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.37966105G>ACA4714413ADRB3c.365C>T (p.Thr122Ile)
n.493C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.37966105G>CCA370695741ADRB3c.365C>G (p.Thr122Ser)
n.493C>G
8g.37966105G=CA1777329266ADRB3c.365C= (p.Thr122=)
n.493C=
8g.37966105G>TCA370695743ADRB3c.365C>A (p.Thr122Asn)
n.493C>A
8g.37966105_37966106insGTGCA175072224ADRB3c.365_366insACC (p.Thr122_Ala123insPro)
n.493_494insACC
dbSNP
8g.37966106T>ACA370695751ADRB3c.364A>T (p.Thr122Ser)
n.492A>T
8g.37966106T>CCA370695753ADRB3c.364A>G (p.Thr122Ala)
n.492A>G
8g.37966106T>GCA175072238ADRB3c.364A>C (p.Thr122Pro)
n.492A>C
dbSNP
8g.37966106T=CA1777329267ADRB3c.364A= (p.Thr122=)
n.492A=
8g.37966107C>ACA460494570ADRB3c.363G>T (p.Val121=)
n.491G>T
8g.37966107C>GCA460494572ADRB3c.363G>C (p.Val121=)
n.491G>C
8g.37966107C>TCA460494573ADRB3c.363G>A (p.Val121=)
n.491G>A
gnomAD v4

Number of alleles fetched