Primary Site >> Stomach Cancer
Gene >> IRF2BPL
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000238647 |
| Start | 77025674:77025674(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2119A>G |
| AA Mutation | p.Met707Val(p.M707V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000238647 |
| Start | 77026768:77026768(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1025G>A |
| AA Mutation | p.Arg342His(p.R342H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000238647 |
| Start | 77026621:77026621(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1172G>A |
| AA Mutation | p.Arg391His(p.R391H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000238647 |
| Start | 77025967:77025967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1826G>A |
| AA Mutation | p.Arg609Gln(p.R609Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000238647 |
| Start | 77026571:77026571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1222G>A |
| AA Mutation | p.Val408Ile(p.V408I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000238647 |
| Start | 77026505:77026505(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1288G>A |
| AA Mutation | p.Val430Met(p.V430M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000238647 |
| Start | 77025667:77025667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2126A>G |
| AA Mutation | p.Asn709Ser(p.N709S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000238647 |
| Start | 77025882:77025882(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1911G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000238647 |
| Start | 77026290:77026290(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs569983748 |
| CDS Mutation | c.1503C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000238647 |
| Start | 77025435:77025435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2358G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |