Primary Site >> Stomach Cancer
Gene >> CYP1A1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379727 |
| Start | 74721293:74721293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371074476 |
| CDS Mutation | c.1072C>T |
| AA Mutation | p.Arg358Trp(p.R358W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379727 |
| Start | 74720538:74720538(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1490C>A |
| AA Mutation | p.Thr497Asn(p.T497N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379727 |
| Start | 74721651:74721651(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.892G>A |
| AA Mutation | p.Ala298Thr(p.A298T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379727 |
| Start | 74720599:74720599(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs56240201 |
| CDS Mutation | c.1429C>T |
| AA Mutation | p.Arg477Trp(p.R477W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379727 |
| Start | 74721298:74721298(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368650547 |
| CDS Mutation | c.1067G>A |
| AA Mutation | p.Arg356Gln(p.R356Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379727 |
| Start | 74722426:74722426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144413202 |
| CDS Mutation | c.672C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379727 |
| Start | 74721652:74721652(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759758088 |
| CDS Mutation | c.891C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000379727 |
| Start | 74721323:74721323(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1043-1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |