Primary Site >> Stomach Cancer
Gene >> CYP2A6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301141 |
| Start | 40846936:40846936(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778072113 |
| CDS Mutation | c.770G>A |
| AA Mutation | p.Arg257His(p.R257H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301141 |
| Start | 40846027:40846027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs60823196 |
| CDS Mutation | c.902G>C |
| AA Mutation | p.Gly301Ala(p.G301A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301141 |
| Start | 40843800:40843800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1481G>A |
| AA Mutation | p.Arg494His(p.R494H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301141 |
| Start | 40846919:40846919(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750403699 |
| CDS Mutation | c.787T>A |
| AA Mutation | p.Ser263Thr(p.S263T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301141 |
| Start | 40848238:40848238(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs185545560 |
| CDS Mutation | c.635C>T |
| AA Mutation | p.Thr212Met(p.T212M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301141 |
| Start | 40848649:40848649(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.458C>T |
| AA Mutation | p.Ala153Val(p.A153V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301141 |
| Start | 40845449:40845449(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374200109 |
| CDS Mutation | c.1006G>A |
| AA Mutation | p.Gly336Ser(p.G336S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301141 |
| Start | 40850347:40850347(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.80G>C |
| AA Mutation | p.Arg27Thr(p.R27T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301141 |
| Start | 40848644:40848644(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.463T>C |
| AA Mutation | p.Phe155Leu(p.F155L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301141 |
| Start | 40846026:40846026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs60988093 |
| CDS Mutation | c.903G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000301141 |
| Start | 40848232:40848287(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.586_641delAAAGAGTTCCTGTCACTGTTGCGCATGATGCTAGGAATCTTCCAGTTCACGTCAAC |
| AA Mutation | p.Lys196LeufsTer7(p.K196Lfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |