Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.37966017C>A | CA370695327 | ADRB3 | c.453G>T (p.Lys151Asn) n.581G>T | gnomAD v4 |
8 | g.37966017C= | CA1777329211 | ADRB3 | c.453G= (p.Lys151=) n.581G= | |
8 | g.37966017C>G | CA370695328 | ADRB3 | c.453G>C (p.Lys151Asn) n.581G>C | dbSNP |
8 | g.37966017C>T | CA460494395 | ADRB3 | c.453G>A (p.Lys151=) n.581G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.37966018T>A | CA370695331 | ADRB3 | c.452A>T (p.Lys151Met) n.580A>T | |
8 | g.37966018T>C | CA4714398 | ADRB3 | c.452A>G (p.Lys151Arg) n.580A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.37966018T>G | CA370695330 | ADRB3 | c.452A>C (p.Lys151Thr) n.580A>C | gnomAD v4 |
8 | g.37966018T= | CA1777329212 | ADRB3 | c.452A= (p.Lys151=) n.580A= | |
8 | g.37966019T>A | CA370695334 | ADRB3 | c.451A>T (p.Lys151Ter) n.579A>T | |
8 | g.37966019T>C | CA370695335 | ADRB3 | c.451A>G (p.Lys151Glu) n.579A>G | |
8 | g.37966019T>G | CA370695337 | ADRB3 | c.451A>C (p.Lys151Gln) n.579A>C | |
8 | g.37966020G>A | CA460494398 | ADRB3 | c.450C>T (p.Thr150=) n.578C>T | |
8 | g.37966020G>C | CA460494399 | ADRB3 | c.450C>G (p.Thr150=) n.578C>G | gnomAD v4 |
8 | g.37966020G>T | CA460494400 | ADRB3 | c.450C>A (p.Thr150=) n.578C>A | gnomAD v4 |
8 | g.37966021G>A | CA370695340 | ADRB3 | c.449C>T (p.Thr150Ile) n.577C>T | |
8 | g.37966021G>C | CA370695341 | ADRB3 | c.449C>G (p.Thr150Ser) n.577C>G | |
8 | g.37966021G= | CA1777329213 | ADRB3 | c.449C= (p.Thr150=) n.577C= | |
8 | g.37966021G>T | CA175072040 | ADRB3 | c.449C>A (p.Thr150Asn) n.577C>A | dbSNP gnomAD v2 gnomAD v4 |
8 | g.37966022T>A | CA370695343 | ADRB3 | c.448A>T (p.Thr150Ser) n.576A>T | gnomAD v4 |
8 | g.37966022T>C | CA370695345 | ADRB3 | c.448A>G (p.Thr150Ala) n.576A>G | |
8 | g.37966022T>G | CA370695346 | ADRB3 | c.448A>C (p.Thr150Pro) n.576A>C | |
8 | g.37966023G>A | CA460494405 | ADRB3 | c.447C>T (p.Val149=) n.575C>T | |
8 | g.37966023G>C | CA460494406 | ADRB3 | c.447C>G (p.Val149=) n.575C>G | |
8 | g.37966023G>T | CA460494407 | ADRB3 | c.447C>A (p.Val149=) n.575C>A | gnomAD v4 |
8 | g.37966024A= | CA1777329214 | ADRB3 | c.446T= (p.Val149=) n.574T= | |
8 | g.37966024A>C | CA370695348 | ADRB3 | c.446T>G (p.Val149Gly) n.574T>G | |
8 | g.37966024A>G | CA370695350 | ADRB3 | c.446T>C (p.Val149Ala) n.574T>C | dbSNP gnomAD v4 |
8 | g.37966024A>T | CA370695352 | ADRB3 | c.446T>A (p.Val149Asp) n.574T>A | |
8 | g.37966024_37966031del | CA2686921917 | ADRB3 | c.439_446del (p.Ala147HisfsTer?) n.567_574del | gnomAD v4 |
8 | g.37966025C>A | CA370695358 | ADRB3 | c.445G>T (p.Val149Phe) n.573G>T | |
8 | g.37966025C>G | CA370695356 | ADRB3 | c.445G>C (p.Val149Leu) n.573G>C | |
8 | g.37966025C>T | CA370695354 | ADRB3 | c.445G>A (p.Val149Ile) n.573G>A | gnomAD v4 |
8 | g.37966026C>A | CA460494411 | ADRB3 | c.444G>T (p.Leu148=) n.572G>T | |
8 | g.37966026C= | CA1777329215 | ADRB3 | c.444G= (p.Leu148=) n.572G= | |
8 | g.37966026C>G | CA460494412 | ADRB3 | c.444G>C (p.Leu148=) n.572G>C | dbSNP gnomAD v2 gnomAD v4 |
8 | g.37966026C>T | CA460494414 | ADRB3 | c.444G>A (p.Leu148=) n.572G>A | |
8 | g.37966027A>C | CA370695359 | ADRB3 | c.443T>G (p.Leu148Arg) n.571T>G | |
8 | g.37966027A>G | CA370695363 | ADRB3 | c.443T>C (p.Leu148Pro) n.571T>C | gnomAD v4 |
8 | g.37966027A>T | CA370695361 | ADRB3 | c.443T>A (p.Leu148Gln) n.571T>A | |
8 | g.37966028G>A | CA4714399 | ADRB3 | c.442C>T (p.Leu148=) n.570C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.37966028G>C | CA370695365 | ADRB3 | c.442C>G (p.Leu148Val) n.570C>G | |
8 | g.37966028G= | CA1777329216 | ADRB3 | c.442C= (p.Leu148=) n.570C= | |
8 | g.37966028G>T | CA370695367 | ADRB3 | c.442C>A (p.Leu148Met) n.570C>A | COSMIC |
8 | g.37966029T>A | CA460494415 | ADRB3 | c.441A>T (p.Ala147=) n.569A>T | |
8 | g.37966029T>C | CA460494416 | ADRB3 | c.441A>G (p.Ala147=) n.569A>G | dbSNP |
8 | g.37966029T>G | CA175072078 | ADRB3 | c.441A>C (p.Ala147=) n.569A>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.37966029T= | CA1777329217 | ADRB3 | c.441A= (p.Ala147=) n.569A= | |
8 | g.37966030G>A | CA370695368 | ADRB3 | c.440C>T (p.Ala147Val) n.568C>T | dbSNP gnomAD v2 |
8 | g.37966030G>C | CA370695370 | ADRB3 | c.440C>G (p.Ala147Gly) n.568C>G | gnomAD v4 |
8 | g.37966030G= | CA1777329218 | ADRB3 | c.440C= (p.Ala147=) n.568C= |