Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.130872895_130872896delinsCT | CA645556982 | ABL1 | c.1000_1001delinsCT (p.Thr334Leu) c.943_944delinsCT (p.Thr315Leu) | COSMIC |
9 | g.130872895_130872896delinsGT | CA645556983 | ABL1 | c.1000_1001delinsGT (p.Thr334Val) c.943_944delinsGT (p.Thr315Val) | COSMIC |
9 | g.130872896C>A | CA375249420 | ABL1 | c.1001C>A (p.Thr334Asn) c.944C>A (p.Thr315Asn) | COSMIC |
9 | g.130872896C= | CA1881475993 | ABL1 | c.1001C= (p.Thr334=) c.944C= (p.Thr315=) | |
9 | g.130872896C>G | CA375249421 | ABL1 | c.1001C>G (p.Thr334Ser) c.944C>G (p.Thr315Ser) | |
9 | g.130872896C>T | CA122575 | ABL1 | c.1001C>T (p.Thr334Ile) c.944C>T (p.Thr315Ile) | ClinVar dbSNP COSMIC COSMIC COSMIC |
9 | g.130872897T>A | CA467395067 | ABL1 | c.1002T>A (p.Thr334=) c.945T>A (p.Thr315=) | |
9 | g.130872897T>C | CA467395068 | ABL1 | c.1002T>C (p.Thr334=) c.945T>C (p.Thr315=) | gnomAD v4 |
9 | g.130872897T>G | CA467395070 | ABL1 | c.1002T>G (p.Thr334=) c.945T>G (p.Thr315=) | dbSNP gnomAD v3 gnomAD v4 |
9 | g.130872897T= | CA1881476000 | ABL1 | c.1002T= (p.Thr334=) c.945T= (p.Thr315=) | |
9 | g.130872898G>A | CA375249422 | ABL1 | c.1003G>A (p.Glu335Lys) c.946G>A (p.Glu316Lys) | |
9 | g.130872898G>C | CA375249423 | ABL1 | c.1003G>C (p.Glu335Gln) c.946G>C (p.Glu316Gln) | |
9 | g.130872898G>T | CA375249424 | ABL1 | c.1003G>T (p.Glu335Ter) c.946G>T (p.Glu316Ter) | |
9 | g.130872899A>C | CA375249425 | ABL1 | c.1004A>C (p.Glu335Ala) c.947A>C (p.Glu316Ala) | |
9 | g.130872899A>G | CA375249426 | ABL1 | c.1004A>G (p.Glu335Gly) c.947A>G (p.Glu316Gly) | |
9 | g.130872899A>T | CA375249427 | ABL1 | c.1004A>T (p.Glu335Val) c.947A>T (p.Glu316Val) | dbSNP |
9 | g.130872900G>A | CA467395074 | ABL1 | c.1005G>A (p.Glu335=) c.948G>A (p.Glu316=) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.130872900G>C | CA375249428 | ABL1 | c.1005G>C (p.Glu335Asp) c.948G>C (p.Glu316Asp) | |
9 | g.130872900G= | CA1881476003 | ABL1 | c.1005G= (p.Glu335=) c.948G= (p.Glu316=) | |
9 | g.130872900G>T | CA375249429 | ABL1 | c.1005G>T (p.Glu335Asp) c.948G>T (p.Glu316Asp) | |
9 | g.130872901T>A | CA16602577 | ABL1 | c.1006T>A (p.Phe336Ile) c.949T>A (p.Phe317Ile) | ClinVar dbSNP |
9 | g.130872901T>C | CA16602794 | ABL1 | c.1006T>C (p.Phe336Leu) c.949T>C (p.Phe317Leu) | ClinVar dbSNP COSMIC |
9 | g.130872901T>G | CA16602578 | ABL1 | c.1006T>G (p.Phe336Val) c.949T>G (p.Phe317Val) | ClinVar dbSNP COSMIC |
9 | g.130872901T= | CA1881476014 | ABL1 | c.1006T= (p.Phe336=) c.949T= (p.Phe317=) | |
9 | g.130872901_130872902delinsCG | CA645556984 | ABL1 | c.1006_1007delinsCG (p.Phe336Arg) c.949_950delinsCG (p.Phe317Arg) | COSMIC |
9 | g.130872902T>A | CA375249430 | ABL1 | c.1007T>A (p.Phe336Tyr) c.950T>A (p.Phe317Tyr) | |
9 | g.130872902T>C | CA375249431 | ABL1 | c.1007T>C (p.Phe336Ser) c.950T>C (p.Phe317Ser) | |
9 | g.130872902T>G | CA16602579 | ABL1 | c.1007T>G (p.Phe336Cys) c.950T>G (p.Phe317Cys) | ClinVar dbSNP |
9 | g.130872902T= | CA1881476025 | ABL1 | c.1007T= (p.Phe336=) c.950T= (p.Phe317=) | |
9 | g.130872903C>A | CA16602554 | ABL1 | c.1008C>A (p.Phe336Leu) c.951C>A (p.Phe317Leu) | ClinVar dbSNP COSMIC |
9 | g.130872903C= | CA1881476034 | ABL1 | c.1008C= (p.Phe336=) c.951C= (p.Phe317=) | |
9 | g.130872903C>G | CA16602555 | ABL1 | c.1008C>G (p.Phe336Leu) c.951C>G (p.Phe317Leu) | ClinVar dbSNP COSMIC |
9 | g.130872903C>T | CA467395081 | ABL1 | c.1008C>T (p.Phe336=) c.951C>T (p.Phe317=) | dbSNP gnomAD v4 |
9 | g.130872904A>C | CA375249432 | ABL1 | c.1009A>C (p.Met337Leu) c.952A>C (p.Met318Leu) | |
9 | g.130872904A>G | CA375249433 | ABL1 | c.1009A>G (p.Met337Val) c.952A>G (p.Met318Val) | |
9 | g.130872904A>T | CA375249434 | ABL1 | c.1009A>T (p.Met337Leu) c.952A>T (p.Met318Leu) | |
9 | g.130872905T>A | CA375249435 | ABL1 | c.1010T>A (p.Met337Lys) c.953T>A (p.Met318Lys) | |
9 | g.130872905T>C | CA375249436 | ABL1 | c.1010T>C (p.Met337Thr) c.953T>C (p.Met318Thr) | |
9 | g.130872905T>G | CA375249437 | ABL1 | c.1010T>G (p.Met337Arg) c.953T>G (p.Met318Arg) | |
9 | g.130872906G>A | CA375249438 | ABL1 | c.1011G>A (p.Met337Ile) c.954G>A (p.Met318Ile) | gnomAD v4 COSMIC |
9 | g.130872906G>C | CA375249439 | ABL1 | c.1011G>C (p.Met337Ile) c.954G>C (p.Met318Ile) | dbSNP |
9 | g.130872906G>T | CA375249440 | ABL1 | c.1011G>T (p.Met337Ile) c.954G>T (p.Met318Ile) | |
9 | g.130872907A>C | CA375249441 | ABL1 | c.1012A>C (p.Thr338Pro) c.955A>C (p.Thr319Pro) | |
9 | g.130872907A>G | CA375249442 | ABL1 | c.1012A>G (p.Thr338Ala) c.955A>G (p.Thr319Ala) | |
9 | g.130872907A>T | CA375249443 | ABL1 | c.1012A>T (p.Thr338Ser) c.955A>T (p.Thr319Ser) | |
9 | g.130872908C>A | CA375249444 | ABL1 | c.1013C>A (p.Thr338Asn) c.956C>A (p.Thr319Asn) | |
9 | g.130872908C>G | CA375249446 | ABL1 | c.1013C>G (p.Thr338Ser) c.956C>G (p.Thr319Ser) | |
9 | g.130872908C>T | CA375249445 | ABL1 | c.1013C>T (p.Thr338Ile) c.956C>T (p.Thr319Ile) | gnomAD v4 COSMIC |
9 | g.130872909C>A | CA467395085 | ABL1 | c.1014C>A (p.Thr338=) c.957C>A (p.Thr319=) | |
9 | g.130872909C= | CA1881476039 | ABL1 | c.1014C= (p.Thr338=) c.957C= (p.Thr319=) |