Primary Site >> Stomach Cancer
Gene >> N4BP2L2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267068 |
| Start | 32522187:32522187(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1468G>A |
| AA Mutation | p.Glu490Lys(p.E490K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399396 |
| Start | 32442429:32442429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2108T>A |
| AA Mutation | p.Phe703Tyr(p.F703Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267068 |
| Start | 32517980:32517980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs117678407 |
| CDS Mutation | c.1574G>A |
| AA Mutation | p.Arg525Gln(p.R525Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399396 |
| Start | 32443854:32443854(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.683A>C |
| AA Mutation | p.Lys228Thr(p.K228T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267068 |
| Start | 32536298:32536298(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.730G>T |
| AA Mutation | p.Asp244Tyr(p.D244Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399396 |
| Start | 32442622:32442622(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1915G>C |
| AA Mutation | p.Glu639Gln(p.E639Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267068 |
| Start | 32535815:32535815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1213A>T |
| AA Mutation | p.Ile405Phe(p.I405F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000399396 |
| Start | 32442821:32442821(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1716A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000399396 |
| Start | 32443288:32443288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746708541 |
| CDS Mutation | c.1249C>T |
| AA Mutation | p.Gln417Ter(p.Q417*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000399396 |
| Start | 32442557:32442558(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1979dupT |
| AA Mutation | p.Leu660PhefsTer3(p.L660Ffs*3) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000399396 |
| Start | 32443547:32443548(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.989dupA |
| AA Mutation | p.Asn330LysfsTer5(p.N330Kfs*5) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000399396 |
| Start | 32443439:32443440(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1097dupT |
| AA Mutation | p.Thr367HisfsTer6(p.T367Hfs*6) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000267068 |
| Start | 32536922:32536923(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.105dupT |
| AA Mutation | p.His36SerfsTer4(p.H36Sfs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |