Primary Site >> Stomach Cancer
Gene >> CYP2B6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324071 |
| Start | 41004368:41004368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774036855 |
| CDS Mutation | c.406G>A |
| AA Mutation | p.Gly136Arg(p.G136R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324071 |
| Start | 41009345:41009345(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.772C>T |
| AA Mutation | p.Pro258Ser(p.P258S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324071 |
| Start | 41016682:41016682(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368451099 |
| CDS Mutation | c.1331C>T |
| AA Mutation | p.Ala444Val(p.A444V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324071 |
| Start | 41009351:41009351(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755100015 |
| CDS Mutation | c.778G>A |
| AA Mutation | p.Ala260Thr(p.A260T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324071 |
| Start | 41004052:41004052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755570515 |
| CDS Mutation | c.223G>A |
| AA Mutation | p.Val75Met(p.V75M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324071 |
| Start | 41010098:41010098(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768992518 |
| CDS Mutation | c.927C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324071 |
| Start | 41016731:41016731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1380C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324071 |
| Start | 41012311:41012311(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.978G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324071 |
| Start | 41016703:41016704(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1352_1353insA |
| AA Mutation | p.Thr452HisfsTer193(p.T452Hfs*193) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324071 |
| Start | 41016764:41016765(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1417dupC |
| AA Mutation | p.Gln473ProfsTer172(p.Q473Pfs*172) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000324071 |
| Start | 41004296:41004296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766031218 |
| CDS Mutation | c.335-1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |