Primary Site >> Stomach Cancer
Gene >> SOCS4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339298 |
| Start | 55043756:55043756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.715A>G |
| AA Mutation | p.Thr239Ala(p.T239A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339298 |
| Start | 55043991:55043991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.950A>G |
| AA Mutation | p.Asp317Gly(p.D317G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339298 |
| Start | 55043291:55043291(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.250C>T |
| AA Mutation | p.His84Tyr(p.H84Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339298 |
| Start | 55044027:55044027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749753893 |
| CDS Mutation | c.986G>A |
| AA Mutation | p.Arg329His(p.R329H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000339298 |
| Start | 55044259:55044259(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779865265 |
| CDS Mutation | c.1218C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000339298 |
| Start | 55043160:55043161(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.125dupA |
| AA Mutation | p.Ser43GlufsTer2(p.S43Efs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |