Primary Site >> Stomach Cancer
Gene >> ABL2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000502732 |
| Start | 179121846:179121846(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781311580 |
| CDS Mutation | c.709C>T |
| AA Mutation | p.Arg237Cys(p.R237C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000502732 |
| Start | 179120239:179120239(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.996A>C |
| AA Mutation | p.Glu332Asp(p.E332D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000502732 |
| Start | 179126513:179126513(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.551A>G |
| AA Mutation | p.Glu184Gly(p.E184G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000502732 |
| Start | 179109004:179109004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377370937 |
| CDS Mutation | c.2263C>T |
| AA Mutation | p.Arg755Cys(p.R755C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000502732 |
| Start | 179108077:179108077(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3190G>T |
| AA Mutation | p.Gly1064Cys(p.G1064C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000502732 |
| Start | 179120201:179120201(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1034T>C |
| AA Mutation | p.Val345Ala(p.V345A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000502732 |
| Start | 179118643:179118643(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1167G>A |
| AA Mutation | p.Met389Ile(p.M389I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000502732 |
| Start | 179108964:179108964(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2303C>T |
| AA Mutation | p.Pro768Leu(p.P768L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000502732 |
| Start | 179109003:179109003(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147435995 |
| CDS Mutation | c.2264G>A |
| AA Mutation | p.Arg755His(p.R755H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000502732 |
| Start | 179117432:179117432(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1308A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000502732 |
| Start | 179108183:179108183(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776713584 |
| CDS Mutation | c.3084C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000502732 |
| Start | 179121792:179121792(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.763C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000502732 |
| Start | 179108881:179108881(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2386delA |
| AA Mutation | p.Arg796GlyfsTer4(p.R796Gfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000502732 |
| Start | 179108759:179108759(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2508delA |
| AA Mutation | p.Lys836AsnfsTer34(p.K836Nfs*34) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000502732 |
| Start | 179108220:179108220(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3047C>G |
| AA Mutation | p.Ser1016Ter(p.S1016*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000502732 |
| Start | 179108347:179108347(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2920C>T |
| AA Mutation | p.Arg974Ter(p.R974*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000502732 |
| Start | 179108575:179108575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2692C>T |
| AA Mutation | p.Arg898Ter(p.R898*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000502732 |
| Start | 179114903:179114904(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs753365868 |
| CDS Mutation | c.1535dupC |
| AA Mutation | p.Lys513Ter(p.K513*) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000502732 |
| Start | 179108758:179108759(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2508dupA |
| AA Mutation | p.Ser837IlefsTer55(p.S837Ifs*55) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |