Primary Site >> Stomach Cancer
Gene >> STAT2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314128 |
| Start | 56355504:56355504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.410C>A |
| AA Mutation | p.Pro137His(p.P137H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314128 |
| Start | 56356477:56356477(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.95G>A |
| AA Mutation | p.Arg32Gln(p.R32Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314128 |
| Start | 56346878:56346878(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1802G>A |
| AA Mutation | p.Arg601His(p.R601H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314128 |
| Start | 56355446:56355446(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.468G>A |
| AA Mutation | p.Met156Ile(p.M156I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314128 |
| Start | 56355472:56355472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.442C>T |
| AA Mutation | p.Arg148Trp(p.R148W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000314128 |
| Start | 56349032:56349033(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs763294380 |
| CDS Mutation | c.1467dupC |
| AA Mutation | p.Lys490GlnfsTer41(p.K490Qfs*41) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |