Primary Site >> Stomach Cancer
Gene >> TRIM32
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373983 |
| Start | 116698772:116698772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1030C>T |
| AA Mutation | p.Arg344Trp(p.R344W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373983 |
| Start | 116699013:116699013(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1271C>T |
| AA Mutation | p.Ala424Val(p.A424V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373983 |
| Start | 116699559:116699559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1817G>A |
| AA Mutation | p.Gly606Glu(p.G606E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373983 |
| Start | 116699268:116699268(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1526G>A |
| AA Mutation | p.Cys509Tyr(p.C509Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373983 |
| Start | 116699396:116699396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1654A>T |
| AA Mutation | p.Ile552Phe(p.I552F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373983 |
| Start | 116698335:116698335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.593A>G |
| AA Mutation | p.Glu198Gly(p.E198G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373983 |
| Start | 116699027:116699027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1285C>A |
| AA Mutation | p.Leu429Ile(p.L429I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373983 |
| Start | 116698504:116698504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747057835 |
| CDS Mutation | c.762G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373983 |
| Start | 116698846:116698846(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1104A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000373983 |
| Start | 116699223:116699223(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1482delG |
| AA Mutation | p.Trp494CysfsTer40(p.W494Cfs*40) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000373983 |
| Start | 116699249:116699249(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1510delG |
| AA Mutation | p.Val504TrpfsTer30(p.V504Wfs*30) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |