Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.29913199A>GCA11497295RBMS3c.885+15724A>G (p.=)
c.939+13444A>G (p.=)
c.978+13444A>G (p.=)
c.936+13444A>G (p.=)
c.888+15724A>G (p.=)
c.654+13444A>G (p.=)
c.612+13444A>G (p.=)
c.940-11098A>G (p.=)
c.786+15724A>G (p.=)
dbSNP gnomAD
3g.29913201C>ACA72138830RBMS3c.885+15726C>A (p.=)
c.939+13446C>A (p.=)
c.978+13446C>A (p.=)
c.936+13446C>A (p.=)
c.888+15726C>A (p.=)
c.654+13446C>A (p.=)
c.612+13446C>A (p.=)
c.940-11096C>A (p.=)
c.786+15726C>A (p.=)
dbSNP
3g.29913203T>CCA914736560RBMS3c.885+15728T>C (p.=)
c.939+13448T>C (p.=)
c.978+13448T>C (p.=)
c.936+13448T>C (p.=)
c.888+15728T>C (p.=)
c.654+13448T>C (p.=)
c.612+13448T>C (p.=)
c.940-11094T>C (p.=)
c.786+15728T>C (p.=)
gnomAD
3g.29913205A>GCA1046396247RBMS3c.885+15730A>G (p.=)
c.939+13450A>G (p.=)
c.978+13450A>G (p.=)
c.936+13450A>G (p.=)
c.888+15730A>G (p.=)
c.654+13450A>G (p.=)
c.612+13450A>G (p.=)
c.940-11092A>G (p.=)
c.786+15730A>G (p.=)
3g.29913206G>ACA1046396249RBMS3c.885+15731G>A (p.=)
c.939+13451G>A (p.=)
c.978+13451G>A (p.=)
c.936+13451G>A (p.=)
c.888+15731G>A (p.=)
c.654+13451G>A (p.=)
c.612+13451G>A (p.=)
c.940-11091G>A (p.=)
c.786+15731G>A (p.=)
3g.29913206G>TCA1046396251RBMS3c.885+15731G>T (p.=)
c.939+13451G>T (p.=)
c.978+13451G>T (p.=)
c.936+13451G>T (p.=)
c.888+15731G>T (p.=)
c.654+13451G>T (p.=)
c.612+13451G>T (p.=)
c.940-11091G>T (p.=)
c.786+15731G>T (p.=)
3g.29913212A>TCA72138831RBMS3c.885+15737A>T (p.=)
c.939+13457A>T (p.=)
c.978+13457A>T (p.=)
c.936+13457A>T (p.=)
c.888+15737A>T (p.=)
c.654+13457A>T (p.=)
c.612+13457A>T (p.=)
c.940-11085A>T (p.=)
c.786+15737A>T (p.=)
dbSNP gnomAD
3g.29913215A>GCA72138832RBMS3c.885+15740A>G (p.=)
c.939+13460A>G (p.=)
c.978+13460A>G (p.=)
c.936+13460A>G (p.=)
c.888+15740A>G (p.=)
c.654+13460A>G (p.=)
c.612+13460A>G (p.=)
c.940-11082A>G (p.=)
c.786+15740A>G (p.=)
dbSNP
3g.29913217T>ACA542085486RBMS3c.885+15742T>A (p.=)
c.939+13462T>A (p.=)
c.978+13462T>A (p.=)
c.936+13462T>A (p.=)
c.888+15742T>A (p.=)
c.654+13462T>A (p.=)
c.612+13462T>A (p.=)
c.940-11080T>A (p.=)
c.786+15742T>A (p.=)
gnomAD
3g.29913218A>GCA72138833RBMS3c.885+15743A>G (p.=)
c.939+13463A>G (p.=)
c.978+13463A>G (p.=)
c.936+13463A>G (p.=)
c.888+15743A>G (p.=)
c.654+13463A>G (p.=)
c.612+13463A>G (p.=)
c.940-11079A>G (p.=)
c.786+15743A>G (p.=)
dbSNP gnomAD
3g.29913225T>CCA72138834RBMS3c.885+15750T>C (p.=)
c.939+13470T>C (p.=)
c.978+13470T>C (p.=)
c.936+13470T>C (p.=)
c.888+15750T>C (p.=)
c.654+13470T>C (p.=)
c.612+13470T>C (p.=)
c.940-11072T>C (p.=)
c.786+15750T>C (p.=)
dbSNP gnomAD
3g.29913225T>GCA542085490RBMS3c.885+15750T>G (p.=)
c.939+13470T>G (p.=)
c.978+13470T>G (p.=)
c.936+13470T>G (p.=)
c.888+15750T>G (p.=)
c.654+13470T>G (p.=)
c.612+13470T>G (p.=)
c.940-11072T>G (p.=)
c.786+15750T>G (p.=)
gnomAD
3g.29913231G>ACA1046396279RBMS3c.885+15756G>A (p.=)
c.939+13476G>A (p.=)
c.978+13476G>A (p.=)
c.936+13476G>A (p.=)
c.888+15756G>A (p.=)
c.654+13476G>A (p.=)
c.612+13476G>A (p.=)
c.940-11066G>A (p.=)
c.786+15756G>A (p.=)
3g.29913232A>GCA1046396280RBMS3c.885+15757A>G (p.=)
c.939+13477A>G (p.=)
c.978+13477A>G (p.=)
c.936+13477A>G (p.=)
c.888+15757A>G (p.=)
c.654+13477A>G (p.=)
c.612+13477A>G (p.=)
c.940-11065A>G (p.=)
c.786+15757A>G (p.=)
3g.29913242A>GCA72138835RBMS3c.885+15767A>G (p.=)
c.939+13487A>G (p.=)
c.978+13487A>G (p.=)
c.936+13487A>G (p.=)
c.888+15767A>G (p.=)
c.654+13487A>G (p.=)
c.612+13487A>G (p.=)
c.940-11055A>G (p.=)
c.786+15767A>G (p.=)
dbSNP gnomAD COSMIC
3g.29913246G>ACA72138836RBMS3c.885+15771G>A (p.=)
c.939+13491G>A (p.=)
c.978+13491G>A (p.=)
c.936+13491G>A (p.=)
c.888+15771G>A (p.=)
c.654+13491G>A (p.=)
c.612+13491G>A (p.=)
c.940-11051G>A (p.=)
c.786+15771G>A (p.=)
dbSNP gnomAD
3g.29913248T>CCA72138837RBMS3c.885+15773T>C (p.=)
c.939+13493T>C (p.=)
c.978+13493T>C (p.=)
c.936+13493T>C (p.=)
c.888+15773T>C (p.=)
c.654+13493T>C (p.=)
c.612+13493T>C (p.=)
c.940-11049T>C (p.=)
c.786+15773T>C (p.=)
dbSNP
3g.29913250A>GCA906048779RBMS3c.885+15775A>G (p.=)
c.939+13495A>G (p.=)
c.978+13495A>G (p.=)
c.936+13495A>G (p.=)
c.888+15775A>G (p.=)
c.654+13495A>G (p.=)
c.612+13495A>G (p.=)
c.940-11047A>G (p.=)
c.786+15775A>G (p.=)
3g.29913250A>TCA1046396286RBMS3c.885+15775A>T (p.=)
c.939+13495A>T (p.=)
c.978+13495A>T (p.=)
c.936+13495A>T (p.=)
c.888+15775A>T (p.=)
c.654+13495A>T (p.=)
c.612+13495A>T (p.=)
c.940-11047A>T (p.=)
c.786+15775A>T (p.=)
3g.29913255G>ACA1046396291RBMS3c.885+15780G>A (p.=)
c.939+13500G>A (p.=)
c.978+13500G>A (p.=)
c.936+13500G>A (p.=)
c.888+15780G>A (p.=)
c.654+13500G>A (p.=)
c.612+13500G>A (p.=)
c.940-11042G>A (p.=)
c.786+15780G>A (p.=)
3g.29913257T>CCA72138838RBMS3c.885+15782T>C (p.=)
c.939+13502T>C (p.=)
c.978+13502T>C (p.=)
c.936+13502T>C (p.=)
c.888+15782T>C (p.=)
c.654+13502T>C (p.=)
c.612+13502T>C (p.=)
c.940-11040T>C (p.=)
c.786+15782T>C (p.=)
dbSNP gnomAD
3g.29913258A>CCA906048785RBMS3c.885+15783A>C (p.=)
c.939+13503A>C (p.=)
c.978+13503A>C (p.=)
c.936+13503A>C (p.=)
c.888+15783A>C (p.=)
c.654+13503A>C (p.=)
c.612+13503A>C (p.=)
c.940-11039A>C (p.=)
c.786+15783A>C (p.=)
3g.29913265C>GCA72138839RBMS3c.885+15790C>G (p.=)
c.939+13510C>G (p.=)
c.978+13510C>G (p.=)
c.936+13510C>G (p.=)
c.888+15790C>G (p.=)
c.654+13510C>G (p.=)
c.612+13510C>G (p.=)
c.940-11032C>G (p.=)
c.786+15790C>G (p.=)
dbSNP
3g.29913266A>GCA72138840RBMS3c.885+15791A>G (p.=)
c.939+13511A>G (p.=)
c.978+13511A>G (p.=)
c.936+13511A>G (p.=)
c.888+15791A>G (p.=)
c.654+13511A>G (p.=)
c.612+13511A>G (p.=)
c.940-11031A>G (p.=)
c.786+15791A>G (p.=)
dbSNP gnomAD
3g.29913270T>GCA72138841RBMS3c.885+15795T>G (p.=)
c.939+13515T>G (p.=)
c.978+13515T>G (p.=)
c.936+13515T>G (p.=)
c.888+15795T>G (p.=)
c.654+13515T>G (p.=)
c.612+13515T>G (p.=)
c.940-11027T>G (p.=)
c.786+15795T>G (p.=)
dbSNP gnomAD
3g.29913271_29913272delCA542085492RBMS3c.885+15796_885+15797del (p.=)
c.939+13516_939+13517del (p.=)
c.978+13516_978+13517del (p.=)
c.936+13516_936+13517del (p.=)
c.888+15796_888+15797del (p.=)
c.654+13516_654+13517del (p.=)
c.612+13516_612+13517del (p.=)
c.940-11026_940-11025del (p.=)
c.786+15796_786+15797del (p.=)
dbSNP gnomAD
3g.29913271A>CCA72138842RBMS3c.885+15796A>C (p.=)
c.939+13516A>C (p.=)
c.978+13516A>C (p.=)
c.936+13516A>C (p.=)
c.888+15796A>C (p.=)
c.654+13516A>C (p.=)
c.612+13516A>C (p.=)
c.940-11026A>C (p.=)
c.786+15796A>C (p.=)
dbSNP
3g.29913271A>GCA72138843RBMS3c.885+15796A>G (p.=)
c.939+13516A>G (p.=)
c.978+13516A>G (p.=)
c.936+13516A>G (p.=)
c.888+15796A>G (p.=)
c.654+13516A>G (p.=)
c.612+13516A>G (p.=)
c.940-11026A>G (p.=)
c.786+15796A>G (p.=)
dbSNP
3g.29913277C>ACA72138844RBMS3c.885+15802C>A (p.=)
c.939+13522C>A (p.=)
c.978+13522C>A (p.=)
c.936+13522C>A (p.=)
c.888+15802C>A (p.=)
c.654+13522C>A (p.=)
c.612+13522C>A (p.=)
c.940-11020C>A (p.=)
c.786+15802C>A (p.=)
dbSNP gnomAD
3g.29913279A>GCA72138845RBMS3c.885+15804A>G (p.=)
c.939+13524A>G (p.=)
c.978+13524A>G (p.=)
c.936+13524A>G (p.=)
c.888+15804A>G (p.=)
c.654+13524A>G (p.=)
c.612+13524A>G (p.=)
c.940-11018A>G (p.=)
c.786+15804A>G (p.=)
dbSNP
3g.29913283T>GCA1046396299RBMS3c.885+15808T>G (p.=)
c.939+13528T>G (p.=)
c.978+13528T>G (p.=)
c.936+13528T>G (p.=)
c.888+15808T>G (p.=)
c.654+13528T>G (p.=)
c.612+13528T>G (p.=)
c.940-11014T>G (p.=)
c.786+15808T>G (p.=)
3g.29913286_29913289delCA72138846RBMS3c.885+15811_885+15814del (p.=)
c.939+13531_939+13534del (p.=)
c.978+13531_978+13534del (p.=)
c.936+13531_936+13534del (p.=)
c.888+15811_888+15814del (p.=)
c.654+13531_654+13534del (p.=)
c.612+13531_612+13534del (p.=)
c.940-11011_940-11008del (p.=)
c.786+15811_786+15814del (p.=)
dbSNP gnomAD
3g.29913287T>CCA72138847RBMS3c.885+15812T>C (p.=)
c.939+13532T>C (p.=)
c.978+13532T>C (p.=)
c.936+13532T>C (p.=)
c.888+15812T>C (p.=)
c.654+13532T>C (p.=)
c.612+13532T>C (p.=)
c.940-11010T>C (p.=)
c.786+15812T>C (p.=)
dbSNP
3g.29913290A>GCA72138848RBMS3c.885+15815A>G (p.=)
c.939+13535A>G (p.=)
c.978+13535A>G (p.=)
c.936+13535A>G (p.=)
c.888+15815A>G (p.=)
c.654+13535A>G (p.=)
c.612+13535A>G (p.=)
c.940-11007A>G (p.=)
c.786+15815A>G (p.=)
dbSNP
3g.29913291T>CCA906048792RBMS3c.885+15816T>C (p.=)
c.939+13536T>C (p.=)
c.978+13536T>C (p.=)
c.936+13536T>C (p.=)
c.888+15816T>C (p.=)
c.654+13536T>C (p.=)
c.612+13536T>C (p.=)
c.940-11006T>C (p.=)
c.786+15816T>C (p.=)
3g.29913294G>TCA72138849RBMS3c.885+15819G>T (p.=)
c.939+13539G>T (p.=)
c.978+13539G>T (p.=)
c.936+13539G>T (p.=)
c.888+15819G>T (p.=)
c.654+13539G>T (p.=)
c.612+13539G>T (p.=)
c.940-11003G>T (p.=)
c.786+15819G>T (p.=)
dbSNP gnomAD

Number of alleles fetched