Primary Site >> Stomach Cancer
Gene >> LIG4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356922 |
| Start | 108209320:108209320(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1949C>A |
| AA Mutation | p.Thr650Asn(p.T650N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356922 |
| Start | 108209531:108209531(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs104894418 |
| CDS Mutation | c.1738C>G |
| AA Mutation | p.Arg580Gly(p.R580G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356922 |
| Start | 108210081:108210081(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1188T>G |
| AA Mutation | p.Ile396Met(p.I396M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356922 |
| Start | 108209438:108209438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs187323251 |
| CDS Mutation | c.1831G>A |
| AA Mutation | p.Ala611Thr(p.A611T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356922 |
| Start | 108209112:108209112(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2157T>A |
| AA Mutation | p.Asp719Glu(p.D719E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356922 |
| Start | 108208657:108208657(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs183928755 |
| CDS Mutation | c.2612G>A |
| AA Mutation | p.Arg871His(p.R871H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356922 |
| Start | 108209405:108209405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1864G>A |
| AA Mutation | p.Glu622Lys(p.E622K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356922 |
| Start | 108208825:108208825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs574090677 |
| CDS Mutation | c.2444G>A |
| AA Mutation | p.Arg815His(p.R815H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356922 |
| Start | 108209576:108209576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140584260 |
| CDS Mutation | c.1693G>A |
| AA Mutation | p.Val565Ile(p.V565I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356922 |
| Start | 108209340:108209340(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1929C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356922 |
| Start | 108210303:108210303(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.966T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356922 |
| Start | 108210960:108210960(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.309A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000356922 |
| Start | 108209794:108209794(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs767195999 |
| CDS Mutation | c.1475delC |
| AA Mutation | p.Pro492LeufsTer21(p.P492Lfs*21) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |