Primary Site >> Stomach Cancer
Gene >> PRDM1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369096 |
| Start | 106095692:106095692(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.369T>A |
| AA Mutation | p.Asn123Lys(p.N123K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369096 |
| Start | 106105001:106105001(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.841G>A |
| AA Mutation | p.Asp281Asn(p.D281N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369096 |
| Start | 106107143:106107143(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748874731 |
| CDS Mutation | c.2135C>T |
| AA Mutation | p.Ala712Val(p.A712V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369096 |
| Start | 106088394:106088394(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.236C>T |
| AA Mutation | p.Ala79Val(p.A79V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369096 |
| Start | 106105689:106105689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1529G>A |
| AA Mutation | p.Cys510Tyr(p.C510Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369096 |
| Start | 106104954:106104954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.794A>G |
| AA Mutation | p.Asp265Gly(p.D265G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369096 |
| Start | 106105895:106105895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1735G>A |
| AA Mutation | p.Val579Ile(p.V579I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369096 |
| Start | 106105633:106105633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747183412 |
| CDS Mutation | c.1473G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |