Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.130862759T>CCA1881462941ABL1c.607-4T>C (n.607-4T>C)
c.550-4T>C (n.550-4T>C)
dbSNP
9g.130862759T=CA1881462942ABL1c.607-4T= (n.607-4T=)
c.550-4T= (n.550-4T=)
9g.130862760C>TCA2720751107ABL1c.607-3C>T (n.607-3C>T)
c.550-3C>T (n.550-3C>T)
dbSNP
9g.130862761A>CCA375262236ABL1c.607-2A>C (n.607-2A>C)
c.550-2A>C (n.550-2A>C)
9g.130862761A>GCA375262238ABL1c.607-2A>G (n.607-2A>G)
c.550-2A>G (n.550-2A>G)
9g.130862761A>TCA375262240ABL1c.607-2A>T (n.607-2A>T)
c.550-2A>T (n.550-2A>T)
9g.130862763_130863035delCA645556968ABL1c.607_879del
c.550_822del
COSMIC
9g.130862762G>ACA375262247ABL1c.607-1G>A (n.607-1G>A)
c.550-1G>A (n.550-1G>A)
9g.130862762G>CCA375262243ABL1c.607-1G>C (n.607-1G>C)
c.550-1G>C (n.550-1G>C)
9g.130862762G>TCA375262245ABL1c.607-1G>T (n.607-1G>T)
c.550-1G>T (n.550-1G>T)
9g.130862763C>ACA375262249ABL1c.607C>A (p.Leu203Ile)
c.550C>A (p.Leu184Ile)
dbSNP gnomAD v2 gnomAD v4
9g.130862763C=CA1881462946ABL1c.607C= (p.Leu203=)
c.550C= (p.Leu184=)
9g.130862763C>GCA375262251ABL1c.607C>G (p.Leu203Val)
c.550C>G (p.Leu184Val)
9g.130862763C>TCA375262252ABL1c.607C>T (p.Leu203Phe)
c.550C>T (p.Leu184Phe)
ClinVar gnomAD v4
9g.130862764T>ACA375262254ABL1c.608T>A (p.Leu203His)
c.551T>A (p.Leu184His)
dbSNP
9g.130862764T>CCA375262256ABL1c.608T>C (p.Leu203Pro)
c.551T>C (p.Leu184Pro)
9g.130862764T>GCA375262257ABL1c.608T>G (p.Leu203Arg)
c.551T>G (p.Leu184Arg)
9g.130862764T=CA1881462950ABL1c.608T= (p.Leu203=)
c.551T= (p.Leu184=)
9g.130862765C>ACA467496165ABL1c.609C>A (p.Leu203=)
c.552C>A (p.Leu184=)
dbSNP
9g.130862765C=CA1881462958ABL1c.609C= (p.Leu203=)
c.552C= (p.Leu184=)
9g.130862765C>GCA467496164ABL1c.609C>G (p.Leu203=)
c.552C>G (p.Leu184=)
dbSNP gnomAD v3 gnomAD v4
9g.130862765C>TCA467496163ABL1c.609C>T (p.Leu203=)
c.552C>T (p.Leu184=)
gnomAD v4
9g.130862766T>ACA375262259ABL1c.610T>A (p.Tyr204Asn)
c.553T>A (p.Tyr185Asn)
9g.130862766T>CCA375262261ABL1c.610T>C (p.Tyr204His)
c.553T>C (p.Tyr185His)
gnomAD v4
9g.130862766T>GCA375262263ABL1c.610T>G (p.Tyr204Asp)
c.553T>G (p.Tyr185Asp)
9g.130862767A>CCA375262265ABL1c.611A>C (p.Tyr204Ser)
c.554A>C (p.Tyr185Ser)
9g.130862767A>GCA375262267ABL1c.611A>G (p.Tyr204Cys)
c.554A>G (p.Tyr185Cys)
gnomAD v4
9g.130862767A>TCA375262269ABL1c.611A>T (p.Tyr204Phe)
c.554A>T (p.Tyr185Phe)
9g.130862768C>ACA375262274ABL1c.612C>A (p.Tyr204Ter)
c.555C>A (p.Tyr185Ter)
9g.130862768C=CA1881462964ABL1c.612C= (p.Tyr204=)
c.555C= (p.Tyr185=)
9g.130862768C>GCA375262271ABL1c.612C>G (p.Tyr204Ter)
c.555C>G (p.Tyr185Ter)
9g.130862768C>TCA200680379ABL1c.612C>T (p.Tyr204=)
c.555C>T (p.Tyr185=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.130862769G>ACA5285247ABL1c.613G>A (p.Val205Ile)
c.556G>A (p.Val186Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
9g.130862769G>CCA375262277ABL1c.613G>C (p.Val205Leu)
c.556G>C (p.Val186Leu)
dbSNP
9g.130862769G=CA1881462970ABL1c.613G= (p.Val205=)
c.556G= (p.Val186=)
9g.130862769G>TCA375262279ABL1c.613G>T (p.Val205Phe)
c.556G>T (p.Val186Phe)
9g.130862770T>ACA375262281ABL1c.614T>A (p.Val205Asp)
c.557T>A (p.Val186Asp)
9g.130862770T>CCA375262282ABL1c.614T>C (p.Val205Ala)
c.557T>C (p.Val186Ala)
9g.130862770T>GCA375262284ABL1c.614T>G (p.Val205Gly)
c.557T>G (p.Val186Gly)
9g.130862771C>ACA467496166ABL1c.615C>A (p.Val205=)
c.558C>A (p.Val186=)
9g.130862771C>GCA467496167ABL1c.615C>G (p.Val205=)
c.558C>G (p.Val186=)
9g.130862771C>TCA467496168ABL1c.615C>T (p.Val205=)
c.558C>T (p.Val186=)
9g.130862772T>ACA375262286ABL1c.616T>A (p.Ser206Thr)
c.559T>A (p.Ser187Thr)
9g.130862772T>CCA200680389ABL1c.616T>C (p.Ser206Pro)
c.559T>C (p.Ser187Pro)
dbSNP
9g.130862772T>GCA375262289ABL1c.616T>G (p.Ser206Ala)
c.559T>G (p.Ser187Ala)
9g.130862772T=CA1881462977ABL1c.616T= (p.Ser206=)
c.559T= (p.Ser187=)
9g.130862773C>ACA375262291ABL1c.617C>A (p.Ser206Tyr)
c.560C>A (p.Ser187Tyr)
9g.130862773C>GCA375262293ABL1c.617C>G (p.Ser206Cys)
c.560C>G (p.Ser187Cys)
9g.130862773C>TCA375262295ABL1c.617C>T (p.Ser206Phe)
c.560C>T (p.Ser187Phe)
dbSNP COSMIC COSMIC COSMIC
9g.130862774C>ACA467496169ABL1c.618C>A (p.Ser206=)
c.561C>A (p.Ser187=)

Number of alleles fetched