Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.130862763_130863035delCA645556968ABL1c.607_879del
c.550_822del
COSMIC
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)
9g.130862969G>ACA467496369ABL1c.813G>A (p.Gln271=)
c.756G>A (p.Gln252=)
dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
9g.130862969G>CCA16602548ABL1c.813G>C (p.Gln271His)
c.756G>C (p.Gln252His)
ClinVar dbSNP COSMIC
9g.130862969G=CA1881463456ABL1c.813G= (p.Gln271=)
c.756G= (p.Gln252=)
9g.130862969G>TCA16602549ABL1c.813G>T (p.Gln271His)
c.756G>T (p.Gln252His)
ClinVar dbSNP COSMIC
9g.130862970T>ACA375263289ABL1c.814T>A (p.Tyr272Asn)
c.757T>A (p.Tyr253Asn)
9g.130862970T>CCA122584ABL1c.814T>C (p.Tyr272His)
c.757T>C (p.Tyr253His)
ClinVar dbSNP COSMIC
9g.130862970T>GCA375263285ABL1c.814T>G (p.Tyr272Asp)
c.757T>G (p.Tyr253Asp)
9g.130862970T=CA1881463460ABL1c.814T= (p.Tyr272=)
c.757T= (p.Tyr253=)
9g.130862971A=CA1881463470ABL1c.815A= (p.Tyr272=)
c.758A= (p.Tyr253=)
9g.130862971A>CCA375263291ABL1c.815A>C (p.Tyr272Ser)
c.758A>C (p.Tyr253Ser)
9g.130862971A>GCA375263294ABL1c.815A>G (p.Tyr272Cys)
c.758A>G (p.Tyr253Cys)
dbSNP
9g.130862971A>TCA16602550ABL1c.815A>T (p.Tyr272Phe)
c.758A>T (p.Tyr253Phe)
ClinVar dbSNP COSMIC
9g.130862972C>ACA375263298ABL1c.816C>A (p.Tyr272Ter)
c.759C>A (p.Tyr253Ter)
9g.130862972C=CA1881463482ABL1c.816C= (p.Tyr272=)
c.759C= (p.Tyr253=)
9g.130862972C>GCA375263299ABL1c.816C>G (p.Tyr272Ter)
c.759C>G (p.Tyr253Ter)
dbSNP
9g.130862972C>TCA5285274ABL1c.816C>T (p.Tyr272=)
c.759C>T (p.Tyr253=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.130862973G>ACA375263307ABL1c.817G>A (p.Gly273Arg)
c.760G>A (p.Gly254Arg)
ClinVar dbSNP gnomAD v4
9g.130862973G>CCA375263309ABL1c.817G>C (p.Gly273Arg)
c.760G>C (p.Gly254Arg)
9g.130862973G=CA1881463488ABL1c.817G= (p.Gly273=)
c.760G= (p.Gly254=)
9g.130862973G>TCA375263311ABL1c.817G>T (p.Gly273Trp)
c.760G>T (p.Gly254Trp)
9g.130862974G>ACA375263313ABL1c.818G>A (p.Gly273Glu)
c.761G>A (p.Gly254Glu)
dbSNP
9g.130862974G>CCA375263314ABL1c.818G>C (p.Gly273Ala)
c.761G>C (p.Gly254Ala)
9g.130862974G=CA1881463500ABL1c.818G= (p.Gly273=)
c.761G= (p.Gly254=)
9g.130862974G>TCA375263315ABL1c.818G>T (p.Gly273Val)
c.761G>T (p.Gly254Val)
9g.130862975G>ACA467496376ABL1c.819G>A (p.Gly273=)
c.762G>A (p.Gly254=)
ClinVar dbSNP gnomAD v4
9g.130862975G>CCA467496378ABL1c.819G>C (p.Gly273=)
c.762G>C (p.Gly254=)
9g.130862975G=CA1881463508ABL1c.819G= (p.Gly273=)
c.762G= (p.Gly254=)
9g.130862975G>TCA467496379ABL1c.819G>T (p.Gly273=)
c.762G>T (p.Gly254=)
9g.130862976G>ACA16602551ABL1c.820G>A (p.Glu274Lys)
c.763G>A (p.Glu255Lys)
ClinVar dbSNP gnomAD v4 COSMIC
9g.130862976G>CCA375263317ABL1c.820G>C (p.Glu274Gln)
c.763G>C (p.Glu255Gln)
gnomAD v4
9g.130862976G=CA1881463513ABL1c.820G= (p.Glu274=)
c.763G= (p.Glu255=)
9g.130862976G>TCA375263320ABL1c.820G>T (p.Glu274Ter)
c.763G>T (p.Glu255Ter)
9g.130862977A=CA1881463524ABL1c.821A= (p.Glu274=)
c.764A= (p.Glu255=)
9g.130862977A>CCA375263323ABL1c.821A>C (p.Glu274Ala)
c.764A>C (p.Glu255Ala)
9g.130862977A>GCA375263326ABL1c.821A>G (p.Glu274Gly)
c.764A>G (p.Glu255Gly)
9g.130862977A>TCA16602552ABL1c.821A>T (p.Glu274Val)
c.764A>T (p.Glu255Val)
ClinVar dbSNP COSMIC
9g.130862978G>ACA467496383ABL1c.822G>A (p.Glu274=)
c.765G>A (p.Glu255=)
dbSNP
9g.130862978G>CCA375263329ABL1c.822G>C (p.Glu274Asp)
c.765G>C (p.Glu255Asp)
9g.130862978G>TCA375263330ABL1c.822G>T (p.Glu274Asp)
c.765G>T (p.Glu255Asp)
gnomAD v4
9g.130862979G>ACA375263333ABL1c.823G>A (p.Val275Met)
c.766G>A (p.Val256Met)
dbSNP
9g.130862979G>CCA375263335ABL1c.823G>C (p.Val275Leu)
c.766G>C (p.Val256Leu)
9g.130862979G>TCA375263336ABL1c.823G>T (p.Val275Leu)
c.766G>T (p.Val256Leu)
9g.130862980T>ACA375263339ABL1c.824T>A (p.Val275Glu)
c.767T>A (p.Val256Glu)
9g.130862980T>CCA5285275ABL1c.824T>C (p.Val275Ala)
c.767T>C (p.Val256Ala)
dbSNP ExAC gnomAD v2 gnomAD v4
9g.130862980T>GCA375263342ABL1c.824T>G (p.Val275Gly)
c.767T>G (p.Val256Gly)
9g.130862980T=CA1881463533ABL1c.824T= (p.Val275=)
c.767T= (p.Val256=)

Number of alleles fetched