Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.130862763_130863035delCA645556968ABL1c.607_879del
c.550_822del
COSMIC
9g.130862955C>ACA375263219ABL1c.799C>A (p.Leu267Met)
c.742C>A (p.Leu248Met)
dbSNP
9g.130862955C=CA1881463407ABL1c.799C= (p.Leu267=)
c.742C= (p.Leu248=)
9g.130862955C>GCA16602546ABL1c.799C>G (p.Leu267Val)
c.742C>G (p.Leu248Val)
ClinVar dbSNP COSMIC
9g.130862955C>TCA467496352ABL1c.799C>T (p.Leu267=)
c.742C>T (p.Leu248=)
9g.130862956T>ACA375263222ABL1c.800T>A (p.Leu267Gln)
c.743T>A (p.Leu248Gln)
9g.130862956T>CCA375263226ABL1c.800T>C (p.Leu267Pro)
c.743T>C (p.Leu248Pro)
9g.130862956T>GCA375263224ABL1c.800T>G (p.Leu267Arg)
c.743T>G (p.Leu248Arg)
COSMIC
9g.130862957G>ACA200680512ABL1c.801G>A (p.Leu267=)
c.744G>A (p.Leu248=)
dbSNP gnomAD v3 gnomAD v4
9g.130862957G>CCA467496354ABL1c.801G>C (p.Leu267=)
c.744G>C (p.Leu248=)
9g.130862957G=CA1881463414ABL1c.801G= (p.Leu267=)
c.744G= (p.Leu248=)
9g.130862957G>TCA467496353ABL1c.801G>T (p.Leu267=)
c.744G>T (p.Leu248=)
9g.130862958G>ACA375263229ABL1c.802G>A (p.Gly268Ser)
c.745G>A (p.Gly249Ser)
9g.130862958G>CCA375263232ABL1c.802G>C (p.Gly268Arg)
c.745G>C (p.Gly249Arg)
9g.130862958G>TCA375263231ABL1c.802G>T (p.Gly268Cys)
c.745G>T (p.Gly249Cys)
9g.130862959G>ACA375263233ABL1c.803G>A (p.Gly268Asp)
c.746G>A (p.Gly249Asp)
9g.130862959G>CCA375263237ABL1c.803G>C (p.Gly268Ala)
c.746G>C (p.Gly249Ala)
9g.130862959G>TCA375263235ABL1c.803G>T (p.Gly268Val)
c.746G>T (p.Gly249Val)
9g.130862960C>ACA467496356ABL1c.804C>A (p.Gly268=)
c.747C>A (p.Gly249=)
9g.130862960C=CA1881463417ABL1c.804C= (p.Gly268=)
c.747C= (p.Gly249=)
9g.130862960C>GCA200680517ABL1c.804C>G (p.Gly268=)
c.747C>G (p.Gly249=)
dbSNP
9g.130862960C>TCA5285272ABL1c.804C>T (p.Gly268=)
c.747C>T (p.Gly249=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC
9g.130862961G>ACA375263241ABL1c.805G>A (p.Gly269Arg)
c.748G>A (p.Gly250Arg)
dbSNP gnomAD v4 COSMIC COSMIC COSMIC
9g.130862961G>CCA375263244ABL1c.805G>C (p.Gly269Arg)
c.748G>C (p.Gly250Arg)
9g.130862961G=CA1881463426ABL1c.805G= (p.Gly269=)
c.748G= (p.Gly250=)
9g.130862961G>TCA375263246ABL1c.805G>T (p.Gly269Trp)
c.748G>T (p.Gly250Trp)
gnomAD v4
9g.130862965delCA2720753810ABL1c.809del (p.Gly270AlafsTer16)
c.752del (p.Gly251AlafsTer16)
dbSNP
9g.130862962G>ACA16602547ABL1c.806G>A (p.Gly269Glu)
c.749G>A (p.Gly250Glu)
ClinVar dbSNP gnomAD v4 COSMIC
9g.130862962G>CCA375263250ABL1c.806G>C (p.Gly269Ala)
c.749G>C (p.Gly250Ala)
9g.130862962G=CA1881463429ABL1c.806G= (p.Gly269=)
c.749G= (p.Gly250=)
9g.130862962G>TCA375263252ABL1c.806G>T (p.Gly269Val)
c.749G>T (p.Gly250Val)
gnomAD v4
9g.130862963G>ACA5285273ABL1c.807G>A (p.Gly269=)
c.750G>A (p.Gly250=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.130862963G>CCA467496357ABL1c.807G>C (p.Gly269=)
c.750G>C (p.Gly250=)
9g.130862963G=CA1881463433ABL1c.807G= (p.Gly269=)
c.750G= (p.Gly250=)
9g.130862963G>TCA467496359ABL1c.807G>T (p.Gly269=)
c.750G>T (p.Gly250=)
dbSNP gnomAD v2
9g.130862964G>ACA375263256ABL1c.808G>A (p.Gly270Ser)
c.751G>A (p.Gly251Ser)
9g.130862964G>CCA375263259ABL1c.808G>C (p.Gly270Arg)
c.751G>C (p.Gly251Arg)
9g.130862964G>TCA375263261ABL1c.808G>T (p.Gly270Cys)
c.751G>T (p.Gly251Cys)
COSMIC
9g.130862965G>ACA375263263ABL1c.809G>A (p.Gly270Asp)
c.752G>A (p.Gly251Asp)
dbSNP
9g.130862965G>CCA375263267ABL1c.809G>C (p.Gly270Ala)
c.752G>C (p.Gly251Ala)
9g.130862965G>TCA375263265ABL1c.809G>T (p.Gly270Val)
c.752G>T (p.Gly251Val)
9g.130862966C>ACA467496362ABL1c.810C>A (p.Gly270=)
c.753C>A (p.Gly251=)
9g.130862966C>GCA467496363ABL1c.810C>G (p.Gly270=)
c.753C>G (p.Gly251=)
dbSNP
9g.130862966C>TCA467496364ABL1c.810C>T (p.Gly270=)
c.753C>T (p.Gly251=)
9g.130862967C>ACA375263268ABL1c.811C>A (p.Gln271Lys)
c.754C>A (p.Gln252Lys)
9g.130862967C>GCA375263270ABL1c.811C>G (p.Gln271Glu)
c.754C>G (p.Gln252Glu)
9g.130862967C>TCA375263272ABL1c.811C>T (p.Gln271Ter)
c.754C>T (p.Gln252Ter)
9g.130862968A>CCA375263276ABL1c.812A>C (p.Gln271Pro)
c.755A>C (p.Gln252Pro)
COSMIC COSMIC COSMIC
9g.130862968A>GCA375263279ABL1c.812A>G (p.Gln271Arg)
c.755A>G (p.Gln252Arg)
gnomAD v4
9g.130862968A>TCA375263281ABL1c.812A>T (p.Gln271Leu)
c.755A>T (p.Gln252Leu)

Number of alleles fetched