Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.37966103C>A | CA370695735 | ADRB3 | c.367G>T (p.Ala123Ser) n.495G>T | gnomAD v4 |
8 | g.37966103C= | CA1777329264 | ADRB3 | c.367G= (p.Ala123=) n.495G= | |
8 | g.37966103C>G | CA370695738 | ADRB3 | c.367G>C (p.Ala123Pro) n.495G>C | |
8 | g.37966103C>T | CA175072217 | ADRB3 | c.367G>A (p.Ala123Thr) n.495G>A | dbSNP gnomAD v4 |
8 | g.37966104G>A | CA460494563 | ADRB3 | c.366C>T (p.Thr122=) n.494C>T | COSMIC |
8 | g.37966104G>C | CA460494564 | ADRB3 | c.366C>G (p.Thr122=) n.494C>G | gnomAD v4 |
8 | g.37966104G= | CA1777329265 | ADRB3 | c.366C= (p.Thr122=) n.494C= | |
8 | g.37966104G>T | CA4714412 | ADRB3 | c.366C>A (p.Thr122=) n.494C>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.37966104_37966105insCCA | CA2968110146 | ADRB3 | c.365_366insTGG (p.Thr122_Ala123insGly) n.493_494insTGG | |
8 | g.37966105G>A | CA4714413 | ADRB3 | c.365C>T (p.Thr122Ile) n.493C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.37966105G>C | CA370695741 | ADRB3 | c.365C>G (p.Thr122Ser) n.493C>G | |
8 | g.37966105G= | CA1777329266 | ADRB3 | c.365C= (p.Thr122=) n.493C= | |
8 | g.37966105G>T | CA370695743 | ADRB3 | c.365C>A (p.Thr122Asn) n.493C>A | |
8 | g.37966105_37966106insGTG | CA175072224 | ADRB3 | c.365_366insACC (p.Thr122_Ala123insPro) n.493_494insACC | dbSNP |
8 | g.37966105_37966106insCA | CA2968110147 | ADRB3 | c.364_365insTG (p.Thr122MetfsTer19) n.492_493insTG | |
8 | g.37966106T>A | CA370695751 | ADRB3 | c.364A>T (p.Thr122Ser) n.492A>T | |
8 | g.37966106T>C | CA370695753 | ADRB3 | c.364A>G (p.Thr122Ala) n.492A>G | |
8 | g.37966106T>G | CA175072238 | ADRB3 | c.364A>C (p.Thr122Pro) n.492A>C | dbSNP |
8 | g.37966106T= | CA1777329267 | ADRB3 | c.364A= (p.Thr122=) n.492A= | |
8 | g.37966107C>A | CA460494570 | ADRB3 | c.363G>T (p.Val121=) n.491G>T | |
8 | g.37966107C>G | CA460494572 | ADRB3 | c.363G>C (p.Val121=) n.491G>C | |
8 | g.37966107C>T | CA460494573 | ADRB3 | c.363G>A (p.Val121=) n.491G>A | gnomAD v4 |
8 | g.37966107_37966108insG | CA2968110148 | ADRB3 | c.362_363insC (p.Thr122AspfsTer?) n.490_491insC | |
8 | g.37966108A>C | CA370695757 | ADRB3 | c.362T>G (p.Val121Gly) n.490T>G | |
8 | g.37966108A>G | CA370695758 | ADRB3 | c.362T>C (p.Val121Ala) n.490T>C | |
8 | g.37966108A>T | CA370695761 | ADRB3 | c.362T>A (p.Val121Glu) n.490T>A | |
8 | g.37966109C>A | CA370695767 | ADRB3 | c.361G>T (p.Val121Leu) n.489G>T | |
8 | g.37966109C>G | CA370695770 | ADRB3 | c.361G>C (p.Val121Leu) n.489G>C | |
8 | g.37966109C>T | CA370695772 | ADRB3 | c.361G>A (p.Val121Met) n.489G>A | |
8 | g.37966110A= | CA1777329268 | ADRB3 | c.360T= (p.Cys120=) n.488T= | |
8 | g.37966110A>C | CA370695775 | ADRB3 | c.360T>G (p.Cys120Trp) n.488T>G | |
8 | g.37966110A>G | CA175072239 | ADRB3 | c.360T>C (p.Cys120=) n.488T>C | dbSNP gnomAD v4 |
8 | g.37966110A>T | CA370695778 | ADRB3 | c.360T>A (p.Cys120Ter) n.488T>A | |
8 | g.37966111C>A | CA370695785 | ADRB3 | c.359G>T (p.Cys120Phe) n.487G>T | |
8 | g.37966111C>G | CA370695783 | ADRB3 | c.359G>C (p.Cys120Ser) n.487G>C | |
8 | g.37966111C>T | CA370695780 | ADRB3 | c.359G>A (p.Cys120Tyr) n.487G>A | |
8 | g.37966112A>C | CA370695786 | ADRB3 | c.358T>G (p.Cys120Gly) n.486T>G | |
8 | g.37966112A>G | CA370695789 | ADRB3 | c.358T>C (p.Cys120Arg) n.486T>C | |
8 | g.37966112A>T | CA370695787 | ADRB3 | c.358T>A (p.Cys120Ser) n.486T>A | |
8 | g.37966113C>A | CA460494586 | ADRB3 | c.357G>T (p.Leu119=) n.485G>T | |
8 | g.37966113C>G | CA460494585 | ADRB3 | c.357G>C (p.Leu119=) n.485G>C | |
8 | g.37966113C>T | CA460494583 | ADRB3 | c.357G>A (p.Leu119=) n.485G>A | |
8 | g.37966114A>C | CA370695790 | ADRB3 | c.356T>G (p.Leu119Arg) n.484T>G | |
8 | g.37966114A>G | CA370695792 | ADRB3 | c.356T>C (p.Leu119Pro) n.484T>C | gnomAD v4 |
8 | g.37966114A>T | CA370695791 | ADRB3 | c.356T>A (p.Leu119Gln) n.484T>A | COSMIC |
8 | g.37966115G>A | CA460494587 | ADRB3 | c.355C>T (p.Leu119=) n.483C>T | |
8 | g.37966115G>C | CA370695793 | ADRB3 | c.355C>G (p.Leu119Val) n.483C>G | |
8 | g.37966115G>T | CA370695794 | ADRB3 | c.355C>A (p.Leu119Met) n.483C>A | |
8 | g.37966116C>A | CA460494589 | ADRB3 | c.354G>T (p.Val118=) n.482G>T | gnomAD v4 |
8 | g.37966116C>G | CA460494593 | ADRB3 | c.354G>C (p.Val118=) n.482G>C |