| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.130862763_130863035del | CA645556968 | ABL1 | c.607_879del c.550_822del | COSMIC |
| 9 | g.130862919G>A | CA122581 | ABL1 | c.763G>A (p.Glu255Lys) c.706G>A (p.Glu236Lys) | ClinVar dbSNP |
| 9 | g.130862919G>C | CA375262933 | ABL1 | c.763G>C (p.Glu255Gln) c.706G>C (p.Glu236Gln) | |
| 9 | g.130862919G= | CA1881463293 | ABL1 | c.763G= (p.Glu255=) c.706G= (p.Glu236=) | |
| 9 | g.130862919G>T | CA375262935 | ABL1 | c.763G>T (p.Glu255Ter) c.706G>T (p.Glu236Ter) | |
| 9 | g.130862920A= | CA1881463302 | ABL1 | c.764A= (p.Glu255=) c.707A= (p.Glu236=) | |
| 9 | g.130862920A>C | CA375262937 | ABL1 | c.764A>C (p.Glu255Ala) c.707A>C (p.Glu236Ala) | |
| 9 | g.130862920A>G | CA375262939 | ABL1 | c.764A>G (p.Glu255Gly) c.707A>G (p.Glu236Gly) | |
| 9 | g.130862920A>T | CA122578 | ABL1 | c.764A>T (p.Glu255Val) c.707A>T (p.Glu236Val) | ClinVar dbSNP |
| 9 | g.130862921G>A | CA467496312 | ABL1 | c.765G>A (p.Glu255=) c.708G>A (p.Glu236=) | dbSNP |
| 9 | g.130862921G>C | CA375262943 | ABL1 | c.765G>C (p.Glu255Asp) c.708G>C (p.Glu236Asp) | |
| 9 | g.130862921G>T | CA375262944 | ABL1 | c.765G>T (p.Glu255Asp) c.708G>T (p.Glu236Asp) | |
| 9 | g.130862922A= | CA1881463330 | ABL1 | c.766A= (p.Met256=) c.709A= (p.Met237=) | |
| 9 | g.130862922A>C | CA375262953 | ABL1 | c.766A>C (p.Met256Leu) c.709A>C (p.Met237Leu) | |
| 9 | g.130862922A>G | CA5285270 | ABL1 | c.766A>G (p.Met256Val) c.709A>G (p.Met237Val) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.130862922A>T | CA375262950 | ABL1 | c.766A>T (p.Met256Leu) c.709A>T (p.Met237Leu) | |
| 9 | g.130862923T>A | CA375262959 | ABL1 | c.767T>A (p.Met256Lys) c.710T>A (p.Met237Lys) | |
| 9 | g.130862923T>C | CA375262962 | ABL1 | c.767T>C (p.Met256Thr) c.710T>C (p.Met237Thr) | |
| 9 | g.130862923T>G | CA375262967 | ABL1 | c.767T>G (p.Met256Arg) c.710T>G (p.Met237Arg) | |
| 9 | g.130862924G>A | CA375262971 | ABL1 | c.768G>A (p.Met256Ile) c.711G>A (p.Met237Ile) | gnomAD v4 |
| 9 | g.130862924G>C | CA375262974 | ABL1 | c.768G>C (p.Met256Ile) c.711G>C (p.Met237Ile) | |
| 9 | g.130862924G>T | CA375262976 | ABL1 | c.768G>T (p.Met256Ile) c.711G>T (p.Met237Ile) | |
| 9 | g.130862925G>A | CA375262982 | ABL1 | c.769G>A (p.Glu257Lys) c.712G>A (p.Glu238Lys) | COSMIC |
| 9 | g.130862925G>C | CA375262989 | ABL1 | c.769G>C (p.Glu257Gln) c.712G>C (p.Glu238Gln) | |
| 9 | g.130862925G>T | CA375262983 | ABL1 | c.769G>T (p.Glu257Ter) c.712G>T (p.Glu238Ter) | |
| 9 | g.130862926A>C | CA375262992 | ABL1 | c.770A>C (p.Glu257Ala) c.713A>C (p.Glu238Ala) | |
| 9 | g.130862926A>G | CA375262994 | ABL1 | c.770A>G (p.Glu257Gly) c.713A>G (p.Glu238Gly) | |
| 9 | g.130862926A>T | CA375262997 | ABL1 | c.770A>T (p.Glu257Val) c.713A>T (p.Glu238Val) | |
| 9 | g.130862927A= | CA1881463336 | ABL1 | c.771A= (p.Glu257=) c.714A= (p.Glu238=) | |
| 9 | g.130862927A>C | CA375263000 | ABL1 | c.771A>C (p.Glu257Asp) c.714A>C (p.Glu238Asp) | |
| 9 | g.130862927A>G | CA467496318 | ABL1 | c.771A>G (p.Glu257=) c.714A>G (p.Glu238=) | dbSNP |
| 9 | g.130862927A>T | CA375263003 | ABL1 | c.771A>T (p.Glu257Asp) c.714A>T (p.Glu238Asp) | |
| 9 | g.130862928C>A | CA375263010 | ABL1 | c.772C>A (p.Arg258Ser) c.715C>A (p.Arg239Ser) | |
| 9 | g.130862928C>G | CA375263018 | ABL1 | c.772C>G (p.Arg258Gly) c.715C>G (p.Arg239Gly) | |
| 9 | g.130862928C>T | CA375263007 | ABL1 | c.772C>T (p.Arg258Cys) c.715C>T (p.Arg239Cys) | ClinVar dbSNP gnomAD v4 |
| 9 | g.130862929G>A | CA375263027 | ABL1 | c.773G>A (p.Arg258His) c.716G>A (p.Arg239His) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.130862929G>C | CA375263022 | ABL1 | c.773G>C (p.Arg258Pro) c.716G>C (p.Arg239Pro) | |
| 9 | g.130862929G= | CA1881463349 | ABL1 | c.773G= (p.Arg258=) c.716G= (p.Arg239=) | |
| 9 | g.130862929G>T | CA375263024 | ABL1 | c.773G>T (p.Arg258Leu) c.716G>T (p.Arg239Leu) | dbSNP |
| 9 | g.130862930C>A | CA467496322 | ABL1 | c.774C>A (p.Arg258=) c.717C>A (p.Arg239=) | |
| 9 | g.130862930C= | CA1881463355 | ABL1 | c.774C= (p.Arg258=) c.717C= (p.Arg239=) | |
| 9 | g.130862930C>G | CA467496324 | ABL1 | c.774C>G (p.Arg258=) c.717C>G (p.Arg239=) | |
| 9 | g.130862930C>T | CA200680489 | ABL1 | c.774C>T (p.Arg258=) c.717C>T (p.Arg239=) | dbSNP gnomAD v4 |
| 9 | g.130862931A>C | CA375263035 | ABL1 | c.775A>C (p.Thr259Pro) c.718A>C (p.Thr240Pro) | |
| 9 | g.130862931A>G | CA375263040 | ABL1 | c.775A>G (p.Thr259Ala) c.718A>G (p.Thr240Ala) | |
| 9 | g.130862931A>T | CA375263043 | ABL1 | c.775A>T (p.Thr259Ser) c.718A>T (p.Thr240Ser) | |
| 9 | g.130862932C>A | CA375263047 | ABL1 | c.776C>A (p.Thr259Lys) c.719C>A (p.Thr240Lys) | |
| 9 | g.130862932C= | CA1881463363 | ABL1 | c.776C= (p.Thr259=) c.719C= (p.Thr240=) | |
| 9 | g.130862932C>G | CA375263049 | ABL1 | c.776C>G (p.Thr259Arg) c.719C>G (p.Thr240Arg) | dbSNP |
| 9 | g.130862932C>T | CA375263051 | ABL1 | c.776C>T (p.Thr259Met) c.719C>T (p.Thr240Met) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |