Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
22 | g.19965038G>A | CA14934404 | COMT | c.615+739G>A (p.=) c.465+739G>A (p.=) c.729+739G>A (p.=) c.1026+739G>A (p.=) c.*73+739G>A (p.=) c.*646G>A (p.=) n.193+739G>A | dbSNP gnomAD |
22 | g.19965039G>C | CA638363561 | COMT | c.615+740G>C (p.=) c.465+740G>C (p.=) c.729+740G>C (p.=) c.1026+740G>C (p.=) c.*73+740G>C (p.=) c.*647G>C (p.=) n.193+740G>C | gnomAD |
22 | g.19965040A>T | CA322121483 | COMT | c.615+741A>T (p.=) c.465+741A>T (p.=) c.729+741A>T (p.=) c.1026+741A>T (p.=) c.*73+741A>T (p.=) c.*648A>T (p.=) n.193+741A>T | dbSNP gnomAD |
22 | g.19965047G>A | CA751483351 | COMT | c.615+748G>A (p.=) c.465+748G>A (p.=) c.729+748G>A (p.=) c.1026+748G>A (p.=) c.*73+748G>A (p.=) c.*655G>A (p.=) n.193+748G>A | |
22 | g.19965048_19965049del | CA322121485 | COMT | c.615+749_615+750del (p.=) c.465+749_465+750del (p.=) c.729+749_729+750del (p.=) c.1026+749_1026+750del (p.=) c.*73+749_*73+750del (p.=) c.*656_*657del (p.=) n.193+749_193+750del | dbSNP |
22 | g.19965050C>T | CA751483354 | COMT | c.615+751C>T (p.=) c.465+751C>T (p.=) c.729+751C>T (p.=) c.1026+751C>T (p.=) c.*73+751C>T (p.=) c.*658C>T (p.=) n.193+751C>T | |
22 | g.19965051G>A | CA322121487 | COMT | c.615+752G>A (p.=) c.465+752G>A (p.=) c.729+752G>A (p.=) c.1026+752G>A (p.=) c.*73+752G>A (p.=) c.*659G>A (p.=) n.193+752G>A | dbSNP |
22 | g.19965055G>A | CA751483357 | COMT | c.615+756G>A (p.=) c.465+756G>A (p.=) c.729+756G>A (p.=) c.1026+756G>A (p.=) c.*73+756G>A (p.=) c.*663G>A (p.=) n.193+756G>A | |
22 | g.19965062C>G | CA322121489 | COMT | c.615+763C>G (p.=) c.465+763C>G (p.=) c.729+763C>G (p.=) c.1026+763C>G (p.=) c.*73+763C>G (p.=) c.*670C>G (p.=) n.193+763C>G | dbSNP |
22 | g.19965062C>T | CA751483362 | COMT | c.615+763C>T (p.=) c.465+763C>T (p.=) c.729+763C>T (p.=) c.1026+763C>T (p.=) c.*73+763C>T (p.=) c.*670C>T (p.=) n.193+763C>T | |
22 | g.19965064C>G | CA751483364 | COMT | c.615+765C>G (p.=) c.465+765C>G (p.=) c.729+765C>G (p.=) c.1026+765C>G (p.=) c.*73+765C>G (p.=) c.*672C>G (p.=) n.193+765C>G | |
22 | g.19965069G>A | CA1024133619 | COMT | c.615+770G>A (p.=) c.465+770G>A (p.=) c.729+770G>A (p.=) c.1026+770G>A (p.=) c.*73+770G>A (p.=) c.*677G>A (p.=) n.193+770G>A | |
22 | g.19965070C>A | CA1024133620 | COMT | c.615+771C>A (p.=) c.465+771C>A (p.=) c.729+771C>A (p.=) c.1026+771C>A (p.=) c.*73+771C>A (p.=) c.*678C>A (p.=) n.193+771C>A | |
22 | g.19965083G>A | CA322121491 | COMT | c.615+784G>A (p.=) c.465+784G>A (p.=) c.729+784G>A (p.=) c.1026+784G>A (p.=) c.*73+784G>A (p.=) c.*691G>A (p.=) n.193+784G>A | dbSNP gnomAD |
22 | g.19965084G>T | CA322121493 | COMT | c.615+785G>T (p.=) c.465+785G>T (p.=) c.729+785G>T (p.=) c.1026+785G>T (p.=) c.*73+785G>T (p.=) c.*692G>T (p.=) n.193+785G>T | dbSNP |
22 | g.19965086C>T | CA322121495 | COMT | c.615+787C>T (p.=) c.465+787C>T (p.=) c.729+787C>T (p.=) c.1026+787C>T (p.=) c.*73+787C>T (p.=) c.*694C>T (p.=) n.193+787C>T | dbSNP |
22 | g.19965087G>A | CA322121497 | COMT | c.615+788G>A (p.=) c.465+788G>A (p.=) c.729+788G>A (p.=) c.1026+788G>A (p.=) c.*73+788G>A (p.=) c.*695G>A (p.=) n.193+788G>A | dbSNP |
22 | g.19965088C>G | CA751483368 | COMT | c.615+789C>G (p.=) c.465+789C>G (p.=) c.729+789C>G (p.=) c.1026+789C>G (p.=) c.*73+789C>G (p.=) c.*696C>G (p.=) n.193+789C>G | |
22 | g.19965093C>A | CA638363562 | COMT | c.615+794C>A (p.=) c.465+794C>A (p.=) c.729+794C>A (p.=) c.1026+794C>A (p.=) c.*73+794C>A (p.=) c.*701C>A (p.=) n.193+794C>A | gnomAD |
22 | g.19965097G>A | CA638363563 | COMT | c.615+798G>A (p.=) c.465+798G>A (p.=) c.729+798G>A (p.=) c.1026+798G>A (p.=) c.*73+798G>A (p.=) c.*705G>A (p.=) n.193+798G>A | gnomAD |
22 | g.19965102C>T | CA322121499 | COMT | c.615+803C>T (p.=) c.465+803C>T (p.=) c.729+803C>T (p.=) c.1026+803C>T (p.=) c.*73+803C>T (p.=) c.*710C>T (p.=) n.193+803C>T | dbSNP gnomAD |
22 | g.19965103G>A | CA322121501 | COMT | c.615+804G>A (p.=) c.465+804G>A (p.=) c.729+804G>A (p.=) c.1026+804G>A (p.=) c.*73+804G>A (p.=) c.*711G>A (p.=) n.193+804G>A | dbSNP gnomAD |
22 | g.19965104G>C | CA751483373 | COMT | c.615+805G>C (p.=) c.465+805G>C (p.=) c.729+805G>C (p.=) c.1026+805G>C (p.=) c.*73+805G>C (p.=) c.*712G>C (p.=) n.193+805G>C | |
22 | g.19965112G>A | CA322121502 | COMT | c.615+813G>A (p.=) c.465+813G>A (p.=) c.729+813G>A (p.=) c.1026+813G>A (p.=) c.*73+813G>A (p.=) c.*720G>A (p.=) n.193+813G>A | dbSNP |
22 | g.19965113G>A | CA1024133630 | COMT | c.615+814G>A (p.=) c.465+814G>A (p.=) c.729+814G>A (p.=) c.1026+814G>A (p.=) c.*73+814G>A (p.=) c.*721G>A (p.=) n.193+814G>A | |
22 | g.19965115A>G | CA1024133631 | COMT | c.615+816A>G (p.=) c.465+816A>G (p.=) c.729+816A>G (p.=) c.1026+816A>G (p.=) c.*73+816A>G (p.=) c.*723A>G (p.=) n.193+816A>G | |
22 | g.19965124A>G | CA322121504 | COMT | c.615+825A>G (p.=) c.465+825A>G (p.=) c.729+825A>G (p.=) c.1026+825A>G (p.=) c.*73+825A>G (p.=) c.*732A>G (p.=) n.193+825A>G | dbSNP |
22 | g.19965137G>A | CA1024133632 | COMT | c.615+838G>A (p.=) c.465+838G>A (p.=) c.729+838G>A (p.=) c.1026+838G>A (p.=) c.*73+838G>A (p.=) c.*745G>A (p.=) n.193+838G>A |