Primary Site >> Stomach Cancer
Gene >> SERPINB2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299502 |
| Start | 63902952:63902952(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.895A>G |
| AA Mutation | p.Lys299Glu(p.K299E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299502 |
| Start | 63891598:63891598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.154G>T |
| AA Mutation | p.Asp52Tyr(p.D52Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299502 |
| Start | 63903088:63903088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748882658 |
| CDS Mutation | c.1031C>T |
| AA Mutation | p.Ser344Leu(p.S344L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299502 |
| Start | 63895288:63895288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.193G>T |
| AA Mutation | p.Ala65Ser(p.A65S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299502 |
| Start | 63895363:63895363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.268T>C |
| AA Mutation | p.Tyr90His(p.Y90H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299502 |
| Start | 63897200:63897200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.398A>C |
| AA Mutation | p.Lys133Thr(p.K133T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000299502 |
| Start | 63901880:63901880(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.676T>C |
| AA Mutation | p.Ser226Pro(p.S226P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299502 |
| Start | 63901815:63901815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.611T>G |
| AA Mutation | p.Phe204Cys(p.F204C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000299502 |
| Start | 63897099:63897099(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.297T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000299502 |
| Start | 63901762:63901762(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.558T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000299502 |
| Start | 63895335:63895335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.240G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000299502 |
| Start | 63897768:63897768(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778529592 |
| CDS Mutation | c.459C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000299502 |
| Start | 63902448:63902448(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.725delA |
| AA Mutation | p.Asn242ThrfsTer5(p.N242Tfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |