Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.110781070A>CCA378380466RBM20c.461A>C (p.Gln154Pro)
c.77A>C (p.Gln26Pro)
c.296A>C (p.Gln99Pro)
10g.110781070A>GCA378380480RBM20c.461A>G (p.Gln154Arg)
c.77A>G (p.Gln26Arg)
c.296A>G (p.Gln99Arg)
10g.110781070A>TCA378380490RBM20c.461A>T (p.Gln154Leu)
c.77A>T (p.Gln26Leu)
c.296A>T (p.Gln99Leu)
10g.110781071A>CCA378380492RBM20c.462A>C (p.Gln154His)
c.78A>C (p.Gln26His)
c.297A>C (p.Gln99His)
10g.110781071A>GCA471506581RBM20c.462A>G (p.Gln154=)
c.78A>G (p.Gln26=)
c.297A>G (p.Gln99=)
 gnomAD v4
10g.110781071A>TCA378380496RBM20c.462A>T (p.Gln154His)
c.78A>T (p.Gln26His)
c.297A>T (p.Gln99His)
10g.110781072C>ACA378380511RBM20c.463C>A (p.His155Asn)
c.79C>A (p.His27Asn)
c.298C>A (p.His100Asn)
10g.110781072C>GCA378380503RBM20c.463C>G (p.His155Asp)
c.79C>G (p.His27Asp)
c.298C>G (p.His100Asp)
10g.110781072C>TCA378380507RBM20c.463C>T (p.His155Tyr)
c.79C>T (p.His27Tyr)
c.298C>T (p.His100Tyr)
 gnomAD v4
10g.110781073A>CCA378380513RBM20c.464A>C (p.His155Pro)
c.80A>C (p.His27Pro)
c.299A>C (p.His100Pro)
10g.110781073A>GCA378380514RBM20c.464A>G (p.His155Arg)
c.80A>G (p.His27Arg)
c.299A>G (p.His100Arg)
 gnomAD v4
10g.110781073A>TCA378380515RBM20c.464A>T (p.His155Leu)
c.80A>T (p.His27Leu)
c.299A>T (p.His100Leu)
 ClinVar dbSNP
10g.110781074T>ACA378380516RBM20c.465T>A (p.His155Gln)
c.81T>A (p.His27Gln)
c.300T>A (p.His100Gln)
 dbSNP gnomAD v3 gnomAD v4
10g.110781074T>CCA133393RBM20c.465T>C (p.His155=)
c.81T>C (p.His27=)
c.300T>C (p.His100=)
 ClinVar dbSNP gnomAD v4
10g.110781074T>GCA378380518RBM20c.465T>G (p.His155Gln)
c.81T>G (p.His27Gln)
c.300T>G (p.His100Gln)
10g.110781077_110781079delCA596112231RBM20c.468_470del (p.Ala157del)
c.84_86del (p.Ala29del)
c.303_305del (p.Ala102del)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.110781075G>ACA378380521RBM20c.466G>A (p.Ala156Thr)
c.82G>A (p.Ala28Thr)
c.301G>A (p.Ala101Thr)
 dbSNP gnomAD v2 gnomAD v4
10g.110781075G>CCA378380525RBM20c.466G>C (p.Ala156Pro)
c.82G>C (p.Ala28Pro)
c.301G>C (p.Ala101Pro)
10g.110781075G>TCA378380529RBM20c.466G>T (p.Ala156Ser)
c.82G>T (p.Ala28Ser)
c.301G>T (p.Ala101Ser)
 gnomAD v4
10g.110781076C>ACA378380533RBM20c.467C>A (p.Ala156Asp)
c.83C>A (p.Ala28Asp)
c.302C>A (p.Ala101Asp)
10g.110781076C>GCA378380534RBM20c.467C>G (p.Ala156Gly)
c.83C>G (p.Ala28Gly)
c.302C>G (p.Ala101Gly)
10g.110781076C>TCA213234643RBM20c.467C>T (p.Ala156Val)
c.83C>T (p.Ala28Val)
c.302C>T (p.Ala101Val)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.110781077T>ACA213234648RBM20c.468T>A (p.Ala156=)
c.84T>A (p.Ala28=)
c.303T>A (p.Ala101=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.110781077T>CCA471506587RBM20c.468T>C (p.Ala156=)
c.84T>C (p.Ala28=)
c.303T>C (p.Ala101=)
10g.110781077T>GCA471506588RBM20c.468T>G (p.Ala156=)
c.84T>G (p.Ala28=)
c.303T>G (p.Ala101=)
10g.110781078G>ACA5688512RBM20c.469G>A (p.Ala157Thr)
c.85G>A (p.Ala29Thr)
c.304G>A (p.Ala102Thr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.110781078G>CCA5688511RBM20c.469G>C (p.Ala157Pro)
c.85G>C (p.Ala29Pro)
c.304G>C (p.Ala102Pro)
 dbSNP ExAC gnomAD v4
10g.110781078G>TCA378380547RBM20c.469G>T (p.Ala157Ser)
c.85G>T (p.Ala29Ser)
c.304G>T (p.Ala102Ser)
 gnomAD v4
10g.110781079C>ACA378380572RBM20c.470C>A (p.Ala157Glu)
c.86C>A (p.Ala29Glu)
c.305C>A (p.Ala102Glu)
 gnomAD v4
10g.110781079C>GCA378380582RBM20c.470C>G (p.Ala157Gly)
c.86C>G (p.Ala29Gly)
c.305C>G (p.Ala102Gly)
10g.110781079C>TCA378380577RBM20c.470C>T (p.Ala157Val)
c.86C>T (p.Ala29Val)
c.305C>T (p.Ala102Val)
 gnomAD v4
10g.110781080A>CCA471506592RBM20c.471A>C (p.Ala157=)
c.87A>C (p.Ala29=)
c.306A>C (p.Ala102=)
10g.110781080A>GCA471506593RBM20c.471A>G (p.Ala157=)
c.87A>G (p.Ala29=)
c.306A>G (p.Ala102=)
10g.110781080A>TCA471506594RBM20c.471A>T (p.Ala157=)
c.87A>T (p.Ala29=)
c.306A>T (p.Ala102=)
10g.110781081G>ACA378380583RBM20c.472G>A (p.Ala158Thr)
c.88G>A (p.Ala30Thr)
c.307G>A (p.Ala103Thr)
10g.110781081G>CCA378380585RBM20c.472G>C (p.Ala158Pro)
c.88G>C (p.Ala30Pro)
c.307G>C (p.Ala103Pro)
10g.110781081G>TCA378380588RBM20c.472G>T (p.Ala158Ser)
c.88G>T (p.Ala30Ser)
c.307G>T (p.Ala103Ser)
 gnomAD v4
10g.110781082C>ACA378380593RBM20c.473C>A (p.Ala158Asp)
c.89C>A (p.Ala30Asp)
c.308C>A (p.Ala103Asp)
10g.110781082C>GCA378380600RBM20c.473C>G (p.Ala158Gly)
c.89C>G (p.Ala30Gly)
c.308C>G (p.Ala103Gly)
10g.110781082C>TCA378380604RBM20c.473C>T (p.Ala158Val)
c.89C>T (p.Ala30Val)
c.308C>T (p.Ala103Val)
 COSMIC
10g.110781083C>ACA471506597RBM20c.474C>A (p.Ala158=)
c.90C>A (p.Ala30=)
c.309C>A (p.Ala103=)
10g.110781083C>GCA471506598RBM20c.474C>G (p.Ala158=)
c.90C>G (p.Ala30=)
c.309C>G (p.Ala103=)
10g.110781083C>TCA471506599RBM20c.474C>T (p.Ala158=)
c.90C>T (p.Ala30=)
c.309C>T (p.Ala103=)
10g.110781084A>CCA378380608RBM20c.475A>C (p.Ile159Leu)
c.91A>C (p.Ile31Leu)
c.310A>C (p.Ile104Leu)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.110781084A>GCA378380610RBM20c.475A>G (p.Ile159Val)
c.91A>G (p.Ile31Val)
c.310A>G (p.Ile104Val)
 ClinVar dbSNP gnomAD v2 gnomAD v4
10g.110781084A>TCA378380611RBM20c.475A>T (p.Ile159Leu)
c.91A>T (p.Ile31Leu)
c.310A>T (p.Ile104Leu)
10g.110781085T>ACA378380616RBM20c.476T>A (p.Ile159Lys)
c.92T>A (p.Ile31Lys)
c.311T>A (p.Ile104Lys)
10g.110781085T>CCA378380620RBM20c.476T>C (p.Ile159Thr)
c.92T>C (p.Ile31Thr)
c.311T>C (p.Ile104Thr)
10g.110781085T>GCA378380622RBM20c.476T>G (p.Ile159Arg)
c.92T>G (p.Ile31Arg)
c.311T>G (p.Ile104Arg)
10g.110781086A>CCA471506601RBM20c.477A>C (p.Ile159=)
c.93A>C (p.Ile31=)
c.312A>C (p.Ile104=)

Number of alleles fetched