| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 8 | g.37965670_37965735del | CA2968109739 | ADRB3 | c.744_809del (p.Glu249_Glu270del) n.872_937del c.228_293del (p.Glu77_Glu98del) n.19_84del | |
| 8 | g.37965691_37965696dup | CA581430196 | ADRB3 | c.782_787dup (p.Pro262_Val263insAlaPro) n.910_915dup c.266_271dup (p.Pro90_Val91insAlaPro) n.57_62dup | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.37965688del | CA2968109783 | ADRB3 | c.785del (p.Pro262ArgfsTer?) n.913del c.269del (p.Pro90ArgfsTer?) n.60del | |
| 8 | g.37965688G>A | CA175071221 | ADRB3 | c.782C>T (p.Ala261Val) n.910C>T c.266C>T (p.Ala89Val) n.57C>T | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.37965688G>C | CA370693483 | ADRB3 | c.782C>G (p.Ala261Gly) n.910C>G c.266C>G (p.Ala89Gly) n.57C>G | dbSNP gnomAD v3 |
| 8 | g.37965688G= | CA1777328925 | ADRB3 | c.782C= (p.Ala261=) n.910C= c.266C= (p.Ala89=) n.57C= | |
| 8 | g.37965688G>T | CA370693479 | ADRB3 | c.782C>A (p.Ala261Asp) n.910C>A c.266C>A (p.Ala89Asp) n.57C>A | |
| 8 | g.37965689C>A | CA370693488 | ADRB3 | c.781G>T (p.Ala261Ser) n.909G>T c.265G>T (p.Ala89Ser) n.56G>T | |
| 8 | g.37965689C>G | CA370693491 | ADRB3 | c.781G>C (p.Ala261Pro) n.909G>C c.265G>C (p.Ala89Pro) n.56G>C | |
| 8 | g.37965689C>T | CA370693492 | ADRB3 | c.781G>A (p.Ala261Thr) n.909G>A c.265G>A (p.Ala89Thr) n.56G>A | gnomAD v4 |
| 8 | g.37965690C>A | CA460494458 | ADRB3 | c.780G>T (p.Pro260=) n.908G>T c.264G>T (p.Pro88=) n.55G>T | gnomAD v4 |
| 8 | g.37965690C= | CA1777328927 | ADRB3 | c.780G= (p.Pro260=) n.908G= c.264G= (p.Pro88=) n.55G= | |
| 8 | g.37965690C>G | CA460494457 | ADRB3 | c.780G>C (p.Pro260=) n.908G>C c.264G>C (p.Pro88=) n.55G>C | dbSNP gnomAD v4 |
| 8 | g.37965690C>T | CA460494456 | ADRB3 | c.780G>A (p.Pro260=) n.908G>A c.264G>A (p.Pro88=) n.55G>A | |
| 8 | g.37965690_37965691delinsCG | CA1777328926 | ADRB3 | c.779_780delinsCG (p.Pro260=) n.907_908delinsCG c.263_264delinsCG (p.Pro88=) n.54_55delinsCG | |
| 8 | g.37965691G>A | CA370693495 | ADRB3 | c.779C>T (p.Pro260Leu) n.907C>T c.263C>T (p.Pro88Leu) n.54C>T | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.37965691G>C | CA370693496 | ADRB3 | c.779C>G (p.Pro260Arg) n.907C>G c.263C>G (p.Pro88Arg) n.54C>G | dbSNP |
| 8 | g.37965691G= | CA1777328928 | ADRB3 | c.779C= (p.Pro260=) n.907C= c.263C= (p.Pro88=) n.54C= | |
| 8 | g.37965691G>T | CA370693502 | ADRB3 | c.779C>A (p.Pro260Gln) n.907C>A c.263C>A (p.Pro88Gln) n.54C>A | |
| 8 | g.37965694del | CA581430197 | ADRB3 | c.779del (p.Pro260ArgfsTer?) n.907del c.263del (p.Pro88ArgfsTer?) n.54del | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.37965691_37965692insTGC | CA2842327659 | ADRB3 | c.778_779insGCA (p.Pro260delinsArgThr) n.906_907insGCA c.262_263insGCA (p.Pro88delinsArgThr) n.53_54insGCA | |
| 8 | g.37965692G>A | CA370693505 | ADRB3 | c.778C>T (p.Pro260Ser) n.906C>T c.262C>T (p.Pro88Ser) n.53C>T | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.37965692G>C | CA370693507 | ADRB3 | c.778C>G (p.Pro260Ala) n.906C>G c.262C>G (p.Pro88Ala) n.53C>G | |
| 8 | g.37965692G= | CA1777328929 | ADRB3 | c.778C= (p.Pro260=) n.906C= c.262C= (p.Pro88=) n.53C= | |
| 8 | g.37965692G>T | CA370693509 | ADRB3 | c.778C>A (p.Pro260Thr) n.906C>A c.262C>A (p.Pro88Thr) n.53C>A | |
| 8 | g.37965693G>A | CA175071231 | ADRB3 | c.777C>T (p.Ala259=) n.905C>T c.261C>T (p.Ala87=) n.52C>T | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.37965693G>C | CA460494466 | ADRB3 | c.777C>G (p.Ala259=) n.905C>G c.261C>G (p.Ala87=) n.52C>G | |
| 8 | g.37965693G= | CA1777328930 | ADRB3 | c.777C= (p.Ala259=) n.905C= c.261C= (p.Ala87=) n.52C= | |
| 8 | g.37965693G>T | CA460494465 | ADRB3 | c.777C>A (p.Ala259=) n.905C>A c.261C>A (p.Ala87=) n.52C>A | gnomAD v4 |
| 8 | g.37965694G>A | CA370693515 | ADRB3 | c.776C>T (p.Ala259Val) n.904C>T c.260C>T (p.Ala87Val) n.51C>T | gnomAD v4 |
| 8 | g.37965694G>C | CA370693516 | ADRB3 | c.776C>G (p.Ala259Gly) n.904C>G c.260C>G (p.Ala87Gly) n.51C>G | |
| 8 | g.37965694G>T | CA370693517 | ADRB3 | c.776C>A (p.Ala259Asp) n.904C>A c.260C>A (p.Ala87Asp) n.51C>A | gnomAD v4 |
| 8 | g.37965695C>A | CA370693530 | ADRB3 | c.775G>T (p.Ala259Ser) n.903G>T c.259G>T (p.Ala87Ser) n.50G>T | |
| 8 | g.37965695C= | CA1777328931 | ADRB3 | c.775G= (p.Ala259=) n.903G= c.259G= (p.Ala87=) n.50G= | |
| 8 | g.37965695C>G | CA370693523 | ADRB3 | c.775G>C (p.Ala259Pro) n.903G>C c.259G>C (p.Ala87Pro) n.50G>C | |
| 8 | g.37965695C>T | CA175071242 | ADRB3 | c.775G>A (p.Ala259Thr) n.903G>A c.259G>A (p.Ala87Thr) n.50G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.37965696C>A | CA460494470 | ADRB3 | c.774G>T (p.Leu258=) n.902G>T c.258G>T (p.Leu86=) n.49G>T | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.37965696C= | CA1777328932 | ADRB3 | c.774G= (p.Leu258=) n.902G= c.258G= (p.Leu86=) n.49G= | |
| 8 | g.37965696C>G | CA460494471 | ADRB3 | c.774G>C (p.Leu258=) n.902G>C c.258G>C (p.Leu86=) n.49G>C | |
| 8 | g.37965696C>T | CA460494472 | ADRB3 | c.774G>A (p.Leu258=) n.902G>A c.258G>A (p.Leu86=) n.49G>A | gnomAD v4 |
| 8 | g.37965697A>C | CA370693533 | ADRB3 | c.773T>G (p.Leu258Arg) n.901T>G c.257T>G (p.Leu86Arg) n.48T>G | |
| 8 | g.37965697A>G | CA370693534 | ADRB3 | c.773T>C (p.Leu258Pro) n.901T>C c.257T>C (p.Leu86Pro) n.48T>C | |
| 8 | g.37965697A>T | CA370693535 | ADRB3 | c.773T>A (p.Leu258Gln) n.901T>A c.257T>A (p.Leu86Gln) n.48T>A | |
| 8 | g.37965698G>A | CA460494476 | ADRB3 | c.772C>T (p.Leu258=) n.900C>T c.256C>T (p.Leu86=) n.47C>T | |
| 8 | g.37965698G>C | CA370693536 | ADRB3 | c.772C>G (p.Leu258Val) n.900C>G c.256C>G (p.Leu86Val) n.47C>G | |
| 8 | g.37965698G>T | CA370693537 | ADRB3 | c.772C>A (p.Leu258Met) n.900C>A c.256C>A (p.Leu86Met) n.47C>A | |
| 8 | g.37965699A>C | CA460494477 | ADRB3 | c.771T>G (p.Ser257=) n.899T>G c.255T>G (p.Ser85=) n.46T>G | |
| 8 | g.37965699A>G | CA460494478 | ADRB3 | c.771T>C (p.Ser257=) n.899T>C c.255T>C (p.Ser85=) n.46T>C | |
| 8 | g.37965699A>T | CA460494479 | ADRB3 | c.771T>A (p.Ser257=) n.899T>A c.255T>A (p.Ser85=) n.46T>A | |
| 8 | g.37965700G>A | CA370693538 | ADRB3 | c.770C>T (p.Ser257Phe) n.898C>T c.254C>T (p.Ser85Phe) n.45C>T | dbSNP gnomAD v3 gnomAD v4 |