Primary Site >> Stomach Cancer
Gene >> CHRNB2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368476 |
| Start | 154571706:154571706(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.883C>T |
| AA Mutation | p.Pro295Ser(p.P295S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368476 |
| Start | 154571581:154571581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.758T>C |
| AA Mutation | p.Ile253Thr(p.I253T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368476 |
| Start | 154571794:154571794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.971G>T |
| AA Mutation | p.Arg324Leu(p.R324L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368476 |
| Start | 154571208:154571208(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.385G>A |
| AA Mutation | p.Val129Met(p.V129M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368476 |
| Start | 154569798:154569798(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771286419 |
| CDS Mutation | c.217C>T |
| AA Mutation | p.Arg73Trp(p.R73W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368476 |
| Start | 154571316:154571316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.493G>A |
| AA Mutation | p.Asp165Asn(p.D165N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368476 |
| Start | 154571844:154571844(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1021G>A |
| AA Mutation | p.Glu341Lys(p.E341K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368476 |
| Start | 154571552:154571552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.729C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368476 |
| Start | 154571264:154571264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.441G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368476 |
| Start | 154571648:154571648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140739605 |
| CDS Mutation | c.825G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |