Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.130862763_130863035delCA645556968ABL1c.607_879del
c.550_822del
COSMIC
9g.130862870G>ACA467496246ABL1c.714G>A (p.Lys238=)
c.657G>A (p.Lys219=)
gnomAD v4
9g.130862870G>CCA375262661ABL1c.714G>C (p.Lys238Asn)
c.657G>C (p.Lys219Asn)
9g.130862870G>TCA375262659ABL1c.714G>T (p.Lys238Asn)
c.657G>T (p.Lys219Asn)
9g.130862871C>ACA375262664ABL1c.715C>A (p.Arg239Ser)
c.658C>A (p.Arg220Ser)
dbSNP gnomAD v3 gnomAD v4
9g.130862871C=CA1881463179ABL1c.715C= (p.Arg239=)
c.658C= (p.Arg220=)
9g.130862871C>GCA375262666ABL1c.715C>G (p.Arg239Gly)
c.658C>G (p.Arg220Gly)
9g.130862871C>TCA5285266ABL1c.715C>T (p.Arg239Cys)
c.658C>T (p.Arg220Cys)
dbSNP ExAC gnomAD v2 gnomAD v4
9g.130862872G>ACA375262671ABL1c.716G>A (p.Arg239His)
c.659G>A (p.Arg220His)
ClinVar dbSNP gnomAD v4
9g.130862872G>CCA375262672ABL1c.716G>C (p.Arg239Pro)
c.659G>C (p.Arg220Pro)
dbSNP
9g.130862872G=CA1881463187ABL1c.716G= (p.Arg239=)
c.659G= (p.Arg220=)
9g.130862872G>TCA5285267ABL1c.716G>T (p.Arg239Leu)
c.659G>T (p.Arg220Leu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.130862873C>ACA467496251ABL1c.717C>A (p.Arg239=)
c.660C>A (p.Arg220=)
9g.130862873C>GCA467496252ABL1c.717C>G (p.Arg239=)
c.660C>G (p.Arg220=)
9g.130862873C>TCA467496255ABL1c.717C>T (p.Arg239=)
c.660C>T (p.Arg220=)
9g.130862874A>CCA375262675ABL1c.718A>C (p.Asn240His)
c.661A>C (p.Asn221His)
9g.130862874A>GCA375262677ABL1c.718A>G (p.Asn240Asp)
c.661A>G (p.Asn221Asp)
9g.130862874A>TCA375262679ABL1c.718A>T (p.Asn240Tyr)
c.661A>T (p.Asn221Tyr)
9g.130862875A>CCA375262683ABL1c.719A>C (p.Asn240Thr)
c.662A>C (p.Asn221Thr)
9g.130862875A>GCA375262685ABL1c.719A>G (p.Asn240Ser)
c.662A>G (p.Asn221Ser)
9g.130862875A>TCA375262687ABL1c.719A>T (p.Asn240Ile)
c.662A>T (p.Asn221Ile)
9g.130862876C>ACA375262690ABL1c.720C>A (p.Asn240Lys)
c.663C>A (p.Asn221Lys)
9g.130862876C>GCA375262692ABL1c.720C>G (p.Asn240Lys)
c.663C>G (p.Asn221Lys)
9g.130862876C>TCA467496259ABL1c.720C>T (p.Asn240=)
c.663C>T (p.Asn221=)
9g.130862877A>CCA375262696ABL1c.721A>C (p.Lys241Gln)
c.664A>C (p.Lys222Gln)
9g.130862877A>GCA375262698ABL1c.721A>G (p.Lys241Glu)
c.664A>G (p.Lys222Glu)
9g.130862877A>TCA375262694ABL1c.721A>T (p.Lys241Ter)
c.664A>T (p.Lys222Ter)
9g.130862878A>CCA375262701ABL1c.722A>C (p.Lys241Thr)
c.665A>C (p.Lys222Thr)
9g.130862878A>GCA375262705ABL1c.722A>G (p.Lys241Arg)
c.665A>G (p.Lys222Arg)
9g.130862878A>TCA375262703ABL1c.722A>T (p.Lys241Met)
c.665A>T (p.Lys222Met)
dbSNP
9g.130862879G>ACA467496260ABL1c.723G>A (p.Lys241=)
c.666G>A (p.Lys222=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.130862879G>CCA375262708ABL1c.723G>C (p.Lys241Asn)
c.666G>C (p.Lys222Asn)
dbSNP
9g.130862879G=CA1881463189ABL1c.723G= (p.Lys241=)
c.666G= (p.Lys222=)
9g.130862879G>TCA375262710ABL1c.723G>T (p.Lys241Asn)
c.666G>T (p.Lys222Asn)
9g.130862880C>ACA375262713ABL1c.724C>A (p.Pro242Thr)
c.667C>A (p.Pro223Thr)
dbSNP
9g.130862880C>GCA375262716ABL1c.724C>G (p.Pro242Ala)
c.667C>G (p.Pro223Ala)
9g.130862880C>TCA375262719ABL1c.724C>T (p.Pro242Ser)
c.667C>T (p.Pro223Ser)
dbSNP
9g.130862881C>ACA375262722ABL1c.725C>A (p.Pro242His)
c.668C>A (p.Pro223His)
9g.130862881C>GCA375262724ABL1c.725C>G (p.Pro242Arg)
c.668C>G (p.Pro223Arg)
9g.130862881C>TCA375262726ABL1c.725C>T (p.Pro242Leu)
c.668C>T (p.Pro223Leu)
9g.130862882C>ACA467496264ABL1c.726C>A (p.Pro242=)
c.669C>A (p.Pro223=)
9g.130862882C=CA1881463195ABL1c.726C= (p.Pro242=)
c.669C= (p.Pro223=)
9g.130862882C>GCA467496266ABL1c.726C>G (p.Pro242=)
c.669C>G (p.Pro223=)
9g.130862882C>TCA467496265ABL1c.726C>T (p.Pro242=)
c.669C>T (p.Pro223=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.130862883A>CCA375262729ABL1c.727A>C (p.Thr243Pro)
c.670A>C (p.Thr224Pro)
9g.130862883A>GCA375262731ABL1c.727A>G (p.Thr243Ala)
c.670A>G (p.Thr224Ala)
gnomAD v4
9g.130862883A>TCA375262734ABL1c.727A>T (p.Thr243Ser)
c.670A>T (p.Thr224Ser)
dbSNP
9g.130862884C>ACA375262741ABL1c.728C>A (p.Thr243Asn)
c.671C>A (p.Thr224Asn)
9g.130862884C>GCA375262739ABL1c.728C>G (p.Thr243Ser)
c.671C>G (p.Thr224Ser)
9g.130862884C>TCA375262737ABL1c.728C>T (p.Thr243Ile)
c.671C>T (p.Thr224Ile)
dbSNP

Number of alleles fetched