| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 8 | g.37966158C>A | CA4714419 | ADRB3 | c.312G>T (p.Pro104=) n.440G>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.37966158C= | CA1777329289 | ADRB3 | c.312G= (p.Pro104=) n.440G= | |
| 8 | g.37966158C>G | CA460494677 | ADRB3 | c.312G>C (p.Pro104=) n.440G>C | |
| 8 | g.37966158C>T | CA460494679 | ADRB3 | c.312G>A (p.Pro104=) n.440G>A | gnomAD v4 |
| 8 | g.37966158_37966184delinsCGGCCAGTGGCCAGTCAGCGCCAAGGT | CA1777329288 | ADRB3 | c.286_312delinsACCTTGGCGCTGACTGGCCACTGGCCG (p.Thr96=) n.414_440delinsACCTTGGCGCTGACTGGCCACTGGCCG | |
| 8 | g.37966159G>A | CA370696160 | ADRB3 | c.311C>T (p.Pro104Leu) n.439C>T | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 8 | g.37966159G>C | CA370696162 | ADRB3 | c.311C>G (p.Pro104Arg) n.439C>G | gnomAD v4 |
| 8 | g.37966159G= | CA1777329290 | ADRB3 | c.311C= (p.Pro104=) n.439C= | |
| 8 | g.37966159G>T | CA370696166 | ADRB3 | c.311C>A (p.Pro104Gln) n.439C>A | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.37966159_37966160insTTGG | CA581430215 | ADRB3 | c.311_312insCAAC (p.Leu105AsnfsTer?) n.439_440insCAAC | dbSNP gnomAD v2 gnomAD v4 |
| 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 gnomAD v4 |
| 8 | g.37966160G>A | CA370696167 | ADRB3 | c.310C>T (p.Pro104Ser) n.438C>T | dbSNP gnomAD v4 |
| 8 | g.37966160G>C | CA370696180 | ADRB3 | c.310C>G (p.Pro104Ala) n.438C>G | |
| 8 | g.37966160G= | CA1777329292 | ADRB3 | c.310C= (p.Pro104=) n.438C= | |
| 8 | g.37966160G>T | CA370696174 | ADRB3 | c.310C>A (p.Pro104Thr) n.438C>A | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.37966164_37966180del | CA4714420 | ADRB3 | c.294_310del (p.Leu99ValfsTer?) n.422_438del | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.37966161C>A | CA370696185 | ADRB3 | c.309G>T (p.Trp103Cys) n.437G>T | |
| 8 | g.37966161C>G | CA370696187 | ADRB3 | c.309G>C (p.Trp103Cys) n.437G>C | |
| 8 | g.37966161C>T | CA370696190 | ADRB3 | c.309G>A (p.Trp103Ter) n.437G>A | gnomAD v4 |
| 8 | g.37966162C>A | CA370696198 | ADRB3 | c.308G>T (p.Trp103Leu) n.436G>T | |
| 8 | g.37966162C= | CA1777329293 | ADRB3 | c.308G= (p.Trp103=) n.436G= | |
| 8 | g.37966162C>G | CA370696200 | ADRB3 | c.308G>C (p.Trp103Ser) n.436G>C | |
| 8 | g.37966162C>T | CA370696206 | ADRB3 | c.308G>A (p.Trp103Ter) n.436G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 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 | dbSNP gnomAD v2 gnomAD v4 |
| 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 | dbSNP gnomAD v4 |
| 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 v2 gnomAD v4 |
| 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 | ClinVar |
| 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 | gnomAD v4 |
| 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 | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.37966170A= | CA1777329298 | ADRB3 | c.300T= (p.Thr100=) n.428T= |