Primary Site >> Stomach Cancer
Gene >> CERS6
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000305747 |
| Start | 168715129:168715129(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.738G>T |
| AA Mutation | p.Glu246Asp(p.E246D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305747 |
| Start | 168456552:168456552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.104C>T |
| AA Mutation | p.Ala35Val(p.A35V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305747 |
| Start | 168561309:168561309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.394T>C |
| AA Mutation | p.Phe132Leu(p.F132L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305747 |
| Start | 168547654:168547654(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.229G>T |
| AA Mutation | p.Ala77Ser(p.A77S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305747 |
| Start | 168547615:168547615(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755919514 |
| CDS Mutation | c.190G>A |
| AA Mutation | p.Ala64Thr(p.A64T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000305747 |
| Start | 168631037:168631037(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.464delA |
| AA Mutation | p.Lys155ArgfsTer38(p.K155Rfs*38) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000305747 |
| Start | 168715076:168715076(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.685C>T |
| AA Mutation | p.Arg229Ter(p.R229*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |