Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.130873011C>ACA375249667ABL1c.1116C>A (p.Tyr372Ter)
c.1059C>A (p.Tyr353Ter)
9g.130873011C>GCA375249668ABL1c.1116C>G (p.Tyr372Ter)
c.1059C>G (p.Tyr353Ter)
9g.130873011C>TCA467395194ABL1c.1116C>T (p.Tyr372=)
c.1059C>T (p.Tyr353=)
dbSNP gnomAD v4
9g.130873012C>ACA375249669ABL1c.1117C>A (p.Leu373Met)
c.1060C>A (p.Leu354Met)
9g.130873012C>GCA375249670ABL1c.1117C>G (p.Leu373Val)
c.1060C>G (p.Leu354Val)
gnomAD v4
9g.130873012C>TCA467395195ABL1c.1117C>T (p.Leu373=)
c.1060C>T (p.Leu354=)
9g.130873013T>ACA375249671ABL1c.1118T>A (p.Leu373Gln)
c.1061T>A (p.Leu354Gln)
dbSNP
9g.130873013T>CCA375249672ABL1c.1118T>C (p.Leu373Pro)
c.1061T>C (p.Leu354Pro)
9g.130873013T>GCA375249673ABL1c.1118T>G (p.Leu373Arg)
c.1061T>G (p.Leu354Arg)
9g.130873014G>ACA200645557ABL1c.1119G>A (p.Leu373=)
c.1062G>A (p.Leu354=)
9g.130873014G>CCA467395199ABL1c.1119G>C (p.Leu373=)
c.1062G>C (p.Leu354=)
9g.130873014G>TCA467395200ABL1c.1119G>T (p.Leu373=)
c.1062G>T (p.Leu354=)
9g.130873015G>ACA375249675ABL1c.1120G>A (p.Glu374Lys)
c.1063G>A (p.Glu355Lys)
9g.130873015G>CCA375249676ABL1c.1120G>C (p.Glu374Gln)
c.1063G>C (p.Glu355Gln)
9g.130873015G>TCA375249674ABL1c.1120G>T (p.Glu374Ter)
c.1063G>T (p.Glu355Ter)
9g.130873016A=CA1881476167ABL1c.1121A= (p.Glu374=)
c.1064A= (p.Glu355=)
9g.130873016A>CCA375249677ABL1c.1121A>C (p.Glu374Ala)
c.1064A>C (p.Glu355Ala)
9g.130873016A>GCA16602556ABL1c.1121A>G (p.Glu374Gly)
c.1064A>G (p.Glu355Gly)
ClinVar dbSNP COSMIC
9g.130873016A>TCA375249678ABL1c.1121A>T (p.Glu374Val)
c.1064A>T (p.Glu355Val)
9g.130873020_130873022dupCA645556985ABL1c.1125_1127dup (p.Lys376_Asn377insLys)
c.1068_1070dup (p.Lys357_Asn358insLys)
COSMIC
9g.130873017G>ACA467395203ABL1c.1122G>A (p.Glu374=)
c.1065G>A (p.Glu355=)
9g.130873017G>CCA375249679ABL1c.1122G>C (p.Glu374Asp)
c.1065G>C (p.Glu355Asp)
9g.130873017G>TCA375249680ABL1c.1122G>T (p.Glu374Asp)
c.1065G>T (p.Glu355Asp)
9g.130873018A=CA1881476171ABL1c.1123A= (p.Lys375=)
c.1066A= (p.Lys356=)
9g.130873018A>CCA375249681ABL1c.1123A>C (p.Lys375Gln)
c.1066A>C (p.Lys356Gln)
9g.130873018A>GCA375249682ABL1c.1123A>G (p.Lys375Glu)
c.1066A>G (p.Lys356Glu)
dbSNP gnomAD v3 gnomAD v4
9g.130873018A>TCA375249683ABL1c.1123A>T (p.Lys375Ter)
c.1066A>T (p.Lys356Ter)
9g.130873019A=CA1881476174ABL1c.1124A= (p.Lys375=)
c.1067A= (p.Lys356=)
9g.130873019A>CCA375249684ABL1c.1124A>C (p.Lys375Thr)
c.1067A>C (p.Lys356Thr)
9g.130873019A>GCA5285369ABL1c.1124A>G (p.Lys375Arg)
c.1067A>G (p.Lys356Arg)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.130873019A>TCA375249685ABL1c.1124A>T (p.Lys375Met)
c.1067A>T (p.Lys356Met)
9g.130873020G>ACA467395205ABL1c.1125G>A (p.Lys375=)
c.1068G>A (p.Lys356=)
gnomAD v4
9g.130873020G>CCA375249686ABL1c.1125G>C (p.Lys375Asn)
c.1068G>C (p.Lys356Asn)
9g.130873020G>TCA375249687ABL1c.1125G>T (p.Lys375Asn)
c.1068G>T (p.Lys356Asn)
9g.130873020_130873021insGAACA645556986ABL1c.1125_1126insGAA (p.Lys375_Lys376insGlu)
c.1068_1069insGAA (p.Lys356_Lys357insGlu)
COSMIC
9g.130873021A>CCA375249690ABL1c.1126A>C (p.Lys376Gln)
c.1069A>C (p.Lys357Gln)
9g.130873021A>GCA375249689ABL1c.1126A>G (p.Lys376Glu)
c.1069A>G (p.Lys357Glu)
9g.130873021A>TCA375249688ABL1c.1126A>T (p.Lys376Ter)
c.1069A>T (p.Lys357Ter)
9g.130873022A>CCA375249691ABL1c.1127A>C (p.Lys376Thr)
c.1070A>C (p.Lys357Thr)
9g.130873022A>GCA375249692ABL1c.1127A>G (p.Lys376Arg)
c.1070A>G (p.Lys357Arg)
COSMIC
9g.130873022A>TCA375249693ABL1c.1127A>T (p.Lys376Ile)
c.1070A>T (p.Lys357Ile)
9g.130873023A>CCA375249694ABL1c.1128A>C (p.Lys376Asn)
c.1071A>C (p.Lys357Asn)
9g.130873023A>GCA467395207ABL1c.1128A>G (p.Lys376=)
c.1071A>G (p.Lys357=)
9g.130873023A>TCA375249695ABL1c.1128A>T (p.Lys376Asn)
c.1071A>T (p.Lys357Asn)
9g.130873024A>CCA375249696ABL1c.1129A>C (p.Asn377His)
c.1072A>C (p.Asn358His)
9g.130873024A>GCA375249697ABL1c.1129A>G (p.Asn377Asp)
c.1072A>G (p.Asn358Asp)
9g.130873024A>TCA375249698ABL1c.1129A>T (p.Asn377Tyr)
c.1072A>T (p.Asn358Tyr)
9g.130873025A>CCA375249699ABL1c.1130A>C (p.Asn377Thr)
c.1073A>C (p.Asn358Thr)
9g.130873025A>GCA375249700ABL1c.1130A>G (p.Asn377Ser)
c.1073A>G (p.Asn358Ser)
9g.130873025A>TCA375249701ABL1c.1130A>T (p.Asn377Ile)
c.1073A>T (p.Asn358Ile)

Number of alleles fetched