Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.37966058C>A | CA370695479 | ADRB3 | c.412G>T (p.Ala138Ser) n.540G>T | dbSNP gnomAD v3 gnomAD v4 |
8 | g.37966058C= | CA1777329237 | ADRB3 | c.412G= (p.Ala138=) n.540G= | |
8 | g.37966058C>G | CA370695481 | ADRB3 | c.412G>C (p.Ala138Pro) n.540G>C | |
8 | g.37966058C>T | CA370695484 | ADRB3 | c.412G>A (p.Ala138Thr) n.540G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.37966059C>A | CA460494480 | ADRB3 | c.411G>T (p.Leu137=) n.539G>T | |
8 | g.37966059C= | CA1777329238 | ADRB3 | c.411G= (p.Leu137=) n.539G= | |
8 | g.37966059C>G | CA460494482 | ADRB3 | c.411G>C (p.Leu137=) n.539G>C | dbSNP gnomAD v2 gnomAD v4 |
8 | g.37966059C>T | CA175072144 | ADRB3 | c.411G>A (p.Leu137=) n.539G>A | dbSNP |
8 | g.37966060A= | CA1777329239 | ADRB3 | c.410T= (p.Leu137=) n.538T= | |
8 | g.37966060A>C | CA370695494 | ADRB3 | c.410T>G (p.Leu137Arg) n.538T>G | |
8 | g.37966060A>G | CA4714402 | ADRB3 | c.410T>C (p.Leu137Pro) n.538T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.37966060A>T | CA370695499 | ADRB3 | c.410T>A (p.Leu137Gln) n.538T>A | dbSNP |
8 | g.37966061G>A | CA460494485 | ADRB3 | c.409C>T (p.Leu137=) n.537C>T | |
8 | g.37966061G>C | CA370695535 | ADRB3 | c.409C>G (p.Leu137Val) n.537C>G | |
8 | g.37966061G>T | CA370695536 | ADRB3 | c.409C>A (p.Leu137Met) n.537C>A | |
8 | g.37966062G>A | CA460494489 | ADRB3 | c.408C>T (p.Tyr136=) n.536C>T | |
8 | g.37966062G>C | CA370695537 | ADRB3 | c.408C>G (p.Tyr136Ter) n.536C>G | |
8 | g.37966062G>T | CA370695538 | ADRB3 | c.408C>A (p.Tyr136Ter) n.536C>A | gnomAD v4 |
8 | g.37966063T>A | CA370695541 | ADRB3 | c.407A>T (p.Tyr136Phe) n.535A>T | |
8 | g.37966063T>C | CA370695542 | ADRB3 | c.407A>G (p.Tyr136Cys) n.535A>G | dbSNP gnomAD v2 gnomAD v4 |
8 | g.37966063T>G | CA370695544 | ADRB3 | c.407A>C (p.Tyr136Ser) n.535A>C | |
8 | g.37966063T= | CA1777329240 | ADRB3 | c.407A= (p.Tyr136=) n.535A= | |
8 | g.37966064A>C | CA370695547 | ADRB3 | c.406T>G (p.Tyr136Asp) n.534T>G | |
8 | g.37966064A>G | CA370695549 | ADRB3 | c.406T>C (p.Tyr136His) n.534T>C | |
8 | g.37966064A>T | CA370695548 | ADRB3 | c.406T>A (p.Tyr136Asn) n.534T>A | |
8 | g.37966065G>A | CA460494493 | ADRB3 | c.405C>T (p.Arg135=) n.533C>T | |
8 | g.37966065G>C | CA460494494 | ADRB3 | c.405C>G (p.Arg135=) n.533C>G | |
8 | g.37966065G>T | CA460494495 | ADRB3 | c.405C>A (p.Arg135=) n.533C>A | |
8 | g.37966066C>A | CA370695551 | ADRB3 | c.404G>T (p.Arg135Leu) n.532G>T | |
8 | g.37966066C>G | CA370695554 | ADRB3 | c.404G>C (p.Arg135Pro) n.532G>C | |
8 | g.37966066C>T | CA370695559 | ADRB3 | c.404G>A (p.Arg135His) n.532G>A | gnomAD v4 |
8 | g.37966067G>A | CA370695564 | ADRB3 | c.403C>T (p.Arg135Cys) n.531C>T | dbSNP gnomAD v2 gnomAD v4 |
8 | g.37966067G>C | CA4714403 | ADRB3 | c.403C>G (p.Arg135Gly) n.531C>G | dbSNP ExAC gnomAD v4 |
8 | g.37966067G= | CA1777329241 | ADRB3 | c.403C= (p.Arg135=) n.531C= | |
8 | g.37966067G>T | CA370695568 | ADRB3 | c.403C>A (p.Arg135Ser) n.531C>A | dbSNP gnomAD v2 |
8 | g.37966068G>A | CA460494499 | ADRB3 | c.402C>T (p.Asp134=) n.530C>T | gnomAD v4 |
8 | g.37966068G>C | CA370695571 | ADRB3 | c.402C>G (p.Asp134Glu) n.530C>G | |
8 | g.37966068G= | CA1777329242 | ADRB3 | c.402C= (p.Asp134=) n.530C= | |
8 | g.37966068G>T | CA370695574 | ADRB3 | c.402C>A (p.Asp134Glu) n.530C>A | dbSNP gnomAD v2 gnomAD v4 |
8 | g.37966069T>A | CA370695579 | ADRB3 | c.401A>T (p.Asp134Val) n.529A>T | |
8 | g.37966069T>C | CA370695581 | ADRB3 | c.401A>G (p.Asp134Gly) n.529A>G | gnomAD v4 |
8 | g.37966069T>G | CA370695582 | ADRB3 | c.401A>C (p.Asp134Ala) n.529A>C | |
8 | g.37966070C>A | CA370695585 | ADRB3 | c.400G>T (p.Asp134Tyr) n.528G>T | |
8 | g.37966070C= | CA1777329243 | ADRB3 | c.400G= (p.Asp134=) n.528G= | |
8 | g.37966070C>G | CA370695590 | ADRB3 | c.400G>C (p.Asp134His) n.528G>C | |
8 | g.37966070C>T | CA370695587 | ADRB3 | c.400G>A (p.Asp134Asn) n.528G>A | dbSNP gnomAD v3 gnomAD v4 |
8 | g.37966071C>A | CA460494507 | ADRB3 | c.399G>T (p.Val133=) n.527G>T | |
8 | g.37966071C>G | CA460494506 | ADRB3 | c.399G>C (p.Val133=) n.527G>C | |
8 | g.37966071C>T | CA460494504 | ADRB3 | c.399G>A (p.Val133=) n.527G>A | gnomAD v4 |
8 | g.37966072A>C | CA370695592 | ADRB3 | c.398T>G (p.Val133Gly) n.526T>G |