Primary Site >> Stomach Cancer
Gene >> NOXA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341349 |
| Start | 137433504:137433504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.961G>A |
| AA Mutation | p.Ala321Thr(p.A321T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341349 |
| Start | 137434286:137434286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371932076 |
| CDS Mutation | c.1378G>A |
| AA Mutation | p.Val460Met(p.V460M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341349 |
| Start | 137430807:137430807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142901709 |
| CDS Mutation | c.636C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000341349 |
| Start | 137434317:137434317(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1413delC |
| AA Mutation | p.Gly472AlafsTer?(p.G472Afs*?) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000341349 |
| Start | 137426269:137426273(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.199_203delAAGGA |
| AA Mutation | p.Lys67HisfsTer26(p.K67Hfs*26) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000341349 |
| Start | 137431278:137431278(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.745delC |
| AA Mutation | p.Leu249SerfsTer66(p.L249Sfs*66) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000341349 |
| Start | 137433217:137433218(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs773184989 |
| CDS Mutation | c.870dupG |
| AA Mutation | p.Pro291AlafsTer7(p.P291Afs*7) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000341349 |
| Start | 137434212:137434213(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1309dupC |
| AA Mutation | p.Leu437ProfsTer13(p.L437Pfs*13) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |