| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 8 | g.37966158_37966184delinsCGGCCAGTGGCCAGTCAGCGCCAAGGT | CA1777329288 | ADRB3 | c.286_312delinsACCTTGGCGCTGACTGGCCACTGGCCG (p.Thr96=) n.414_440delinsACCTTGGCGCTGACTGGCCACTGGCCG | |
| 8 | g.37966159_37966176delinsGGCCAGTGGCCAGTCAGC | CA1777329291 | ADRB3 | c.294_311delinsGCTGACTGGCCACTGGCC (p.Ala98=) n.422_439delinsGCTGACTGGCCACTGGCC | |
| 8 | g.37966163_37966188del | CA175072285 | ADRB3 | c.286_311del (p.Thr96ValfsTer?) n.414_439del | dbSNP |
| 8 | g.37966164_37966180del | CA4714420 | ADRB3 | c.294_310del (p.Leu99ValfsTer?) n.422_438del | dbSNP ExAC gnomAD |
| 8 | g.37966163A>C | CA370696210 | ADRB3 | c.307T>G (p.Trp103Gly) n.435T>G | |
| 8 | g.37966163A>G | CA370696211 | ADRB3 | c.307T>C (p.Trp103Arg) n.435T>C | |
| 8 | g.37966163A>T | CA370696212 | ADRB3 | c.307T>A (p.Trp103Arg) n.435T>A | |
| 8 | g.37966164G>A | CA460494690 | ADRB3 | c.306C>T (p.His102=) n.434C>T | |
| 8 | g.37966164G>C | CA370696214 | ADRB3 | c.306C>G (p.His102Gln) n.434C>G | gnomAD |
| 8 | g.37966164G= | CA1777329294 | ADRB3 | c.306C= (p.His102=) n.434C= | |
| 8 | g.37966164G>T | CA370696215 | ADRB3 | c.306C>A (p.His102Gln) n.434C>A | |
| 8 | g.37966165T>A | CA370696233 | ADRB3 | c.305A>T (p.His102Leu) n.433A>T | |
| 8 | g.37966165T>C | CA370696230 | ADRB3 | c.305A>G (p.His102Arg) n.433A>G | |
| 8 | g.37966165T>G | CA370696224 | ADRB3 | c.305A>C (p.His102Pro) n.433A>C | |
| 8 | g.37966166G>A | CA370696241 | ADRB3 | c.304C>T (p.His102Tyr) n.432C>T | |
| 8 | g.37966166G>C | CA370696243 | ADRB3 | c.304C>G (p.His102Asp) n.432C>G | |
| 8 | g.37966166G= | CA1777329295 | ADRB3 | c.304C= (p.His102=) n.432C= | |
| 8 | g.37966166G>T | CA370696242 | ADRB3 | c.304C>A (p.His102Asn) n.432C>A | |
| 8 | g.37966167G>A | CA4714421 | ADRB3 | c.303C>T (p.Gly101=) n.431C>T | dbSNP ExAC gnomAD |
| 8 | g.37966167G>C | CA460494693 | ADRB3 | c.303C>G (p.Gly101=) n.431C>G | |
| 8 | g.37966167G= | CA1777329296 | ADRB3 | c.303C= (p.Gly101=) n.431C= | |
| 8 | g.37966167G>T | CA460494694 | ADRB3 | c.303C>A (p.Gly101=) n.431C>A | |
| 8 | g.37966168C>A | CA370696244 | ADRB3 | c.302G>T (p.Gly101Val) n.430G>T | |
| 8 | g.37966168C>G | CA370696245 | ADRB3 | c.302G>C (p.Gly101Ala) n.430G>C | |
| 8 | g.37966168C>T | CA370696246 | ADRB3 | c.302G>A (p.Gly101Asp) n.430G>A | |
| 8 | g.37966169C>A | CA370696263 | ADRB3 | c.301G>T (p.Gly101Cys) n.429G>T | |
| 8 | g.37966169C= | CA1777329297 | ADRB3 | c.301G= (p.Gly101=) n.429G= | |
| 8 | g.37966169C>G | CA370696268 | ADRB3 | c.301G>C (p.Gly101Arg) n.429G>C | |
| 8 | g.37966169C>T | CA370696275 | ADRB3 | c.301G>A (p.Gly101Ser) n.429G>A | gnomAD |
| 8 | g.37966170A= | CA1777329298 | ADRB3 | c.300T= (p.Thr100=) n.428T= | |
| 8 | g.37966170A>C | CA4714422 | ADRB3 | c.300T>G (p.Thr100=) n.428T>G | dbSNP ExAC gnomAD |
| 8 | g.37966170A>G | CA460494698 | ADRB3 | c.300T>C (p.Thr100=) n.428T>C | |
| 8 | g.37966170A>T | CA460494699 | ADRB3 | c.300T>A (p.Thr100=) n.428T>A | gnomAD |
| 8 | g.37966171G>A | CA4714423 | ADRB3 | c.299C>T (p.Thr100Ile) n.427C>T | dbSNP ExAC gnomAD |
| 8 | g.37966171G>C | CA370696286 | ADRB3 | c.299C>G (p.Thr100Ser) n.427C>G | |
| 8 | g.37966171G= | CA1777329299 | ADRB3 | c.299C= (p.Thr100=) n.427C= | |
| 8 | g.37966171G>T | CA370696287 | ADRB3 | c.299C>A (p.Thr100Asn) n.427C>A | |
| 8 | g.37966172T>A | CA370696298 | ADRB3 | c.298A>T (p.Thr100Ser) n.426A>T | |
| 8 | g.37966172T>C | CA175072320 | ADRB3 | c.298A>G (p.Thr100Ala) n.426A>G | dbSNP |
| 8 | g.37966172T>G | CA370696293 | ADRB3 | c.298A>C (p.Thr100Pro) n.426A>C | |
| 8 | g.37966172T= | CA1777329300 | ADRB3 | c.298A= (p.Thr100=) n.426A= | |
| 8 | g.37966173C>A | CA460494703 | ADRB3 | c.297G>T (p.Leu99=) n.425G>T | |
| 8 | g.37966173C>G | CA460494706 | ADRB3 | c.297G>C (p.Leu99=) n.425G>C | |
| 8 | g.37966173C>T | CA460494705 | ADRB3 | c.297G>A (p.Leu99=) n.425G>A | |
| 8 | g.37966174A>C | CA370696302 | ADRB3 | c.296T>G (p.Leu99Arg) n.424T>G | |
| 8 | g.37966174A>G | CA370696303 | ADRB3 | c.296T>C (p.Leu99Pro) n.424T>C | |
| 8 | g.37966174A>T | CA370696304 | ADRB3 | c.296T>A (p.Leu99Gln) n.424T>A | |
| 8 | g.37966175G>A | CA460494707 | ADRB3 | c.295C>T (p.Leu99=) n.423C>T | |
| 8 | g.37966175G>C | CA370696305 | ADRB3 | c.295C>G (p.Leu99Val) n.423C>G | |
| 8 | g.37966175G>T | CA370696306 | ADRB3 | c.295C>A (p.Leu99Met) n.423C>A |