Primary Site >> Stomach Cancer
Gene >> LUM
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266718 |
| Start | 91108706:91108706(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.274C>A |
| AA Mutation | p.Leu92Met(p.L92M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266718 |
| Start | 91104194:91104194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777345268 |
| CDS Mutation | c.988C>T |
| AA Mutation | p.Arg330Cys(p.R330C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266718 |
| Start | 91108262:91108262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs267603717 |
| CDS Mutation | c.718G>A |
| AA Mutation | p.Glu240Lys(p.E240K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266718 |
| Start | 91108300:91108300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.680G>A |
| AA Mutation | p.Arg227His(p.R227H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266718 |
| Start | 91108346:91108346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749360955 |
| CDS Mutation | c.634T>G |
| AA Mutation | p.Leu212Val(p.L212V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266718 |
| Start | 91108504:91108504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.476T>G |
| AA Mutation | p.Val159Gly(p.V159G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266718 |
| Start | 91104238:91104238(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139919924 |
| CDS Mutation | c.944G>A |
| AA Mutation | p.Arg315His(p.R315H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000266718 |
| Start | 91108905:91108905(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.75delT |
| AA Mutation | p.Leu27TyrfsTer30(p.L27Yfs*30) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant;start_lost |
| Transcription ID | ENST00000266718 |
| Start | 91108979:91108979(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1delA |
| AA Mutation | p.Met1?(p.M1?) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |