Chr Mutation (hg38) CAid Gene Transcript Linkouts
22g.19965038G>ACA14934404COMTc.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
22g.19965039G>CCA638363561COMTc.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
22g.19965040A>TCA322121483COMTc.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
22g.19965047G>ACA751483351COMTc.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
22g.19965048_19965049delCA322121485COMTc.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
22g.19965050C>TCA751483354COMTc.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
22g.19965051G>ACA322121487COMTc.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
22g.19965055G>ACA751483357COMTc.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
22g.19965062C>GCA322121489COMTc.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
22g.19965062C>TCA751483362COMTc.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
22g.19965064C>GCA751483364COMTc.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
22g.19965069G>ACA1024133619COMTc.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
22g.19965070C>ACA1024133620COMTc.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
22g.19965083G>ACA322121491COMTc.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
22g.19965084G>TCA322121493COMTc.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
22g.19965086C>TCA322121495COMTc.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
22g.19965087G>ACA322121497COMTc.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
22g.19965088C>GCA751483368COMTc.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
22g.19965093C>ACA638363562COMTc.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
22g.19965097G>ACA638363563COMTc.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
22g.19965102C>TCA322121499COMTc.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
22g.19965103G>ACA322121501COMTc.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
22g.19965104G>CCA751483373COMTc.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
22g.19965112G>ACA322121502COMTc.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
22g.19965113G>ACA1024133630COMTc.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
22g.19965115A>GCA1024133631COMTc.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
22g.19965124A>GCA322121504COMTc.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
22g.19965137G>ACA1024133632COMTc.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

Number of alleles fetched