Primary Site >> Stomach Cancer
Gene >> CEBPZ
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234170 |
| Start | 37213894:37213894(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770254106 |
| CDS Mutation | c.2515G>A |
| AA Mutation | p.Val839Met(p.V839M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234170 |
| Start | 37227785:37227785(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs527616050 |
| CDS Mutation | c.1408C>T |
| AA Mutation | p.Arg470Trp(p.R470W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000234170 |
| Start | 37214887:37214887(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2446A>G |
| AA Mutation | p.Arg816Gly(p.R816G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234170 |
| Start | 37227554:37227554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768232491 |
| CDS Mutation | c.1639G>A |
| AA Mutation | p.Ala547Thr(p.A547T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234170 |
| Start | 37211960:37211960(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2683A>G |
| AA Mutation | p.Asn895Asp(p.N895D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234170 |
| Start | 37228406:37228406(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.787C>A |
| AA Mutation | p.Leu263Ile(p.L263I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234170 |
| Start | 37223375:37223375(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756220214 |
| CDS Mutation | c.1676C>T |
| AA Mutation | p.Thr559Met(p.T559M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000234170 |
| Start | 37227594:37227594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1599A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000234170 |
| Start | 37231421:37231421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.147A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000234170 |
| Start | 37228737:37228737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.456T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000234170 |
| Start | 37231550:37231550(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.18G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000234170 |
| Start | 37228521:37228521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746741037 |
| CDS Mutation | c.672G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000234170 |
| Start | 37227765:37227766(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1427_1428delAA |
| AA Mutation | p.Lys476ArgfsTer3(p.K476Rfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000234170 |
| Start | 37213954:37213954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757023726 |
| CDS Mutation | c.2455A>T |
| AA Mutation | p.Lys819Ter(p.K819*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | splice_donor_variant;coding_sequence_variant;intron_variant |
| Transcription ID | ENST00000234170 |
| Start | 37216311:37216318(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2309_2311+5delAAGGTATG |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |