Primary Site >> Stomach Cancer
Gene >> TRIM41
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315073 |
| Start | 181224586:181224586(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.587G>A |
| AA Mutation | p.Arg196His(p.R196H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315073 |
| Start | 181234180:181234180(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1298T>G |
| AA Mutation | p.Leu433Arg(p.L433R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315073 |
| Start | 181224617:181224617(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.618G>C |
| AA Mutation | p.Gln206His(p.Q206H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315073 |
| Start | 181232794:181232794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1045G>A |
| AA Mutation | p.Ala349Thr(p.A349T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315073 |
| Start | 181234483:181234483(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755074419 |
| CDS Mutation | c.1601G>A |
| AA Mutation | p.Arg534His(p.R534H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315073 |
| Start | 181234326:181234326(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779241234 |
| CDS Mutation | c.1444C>T |
| AA Mutation | p.Arg482Cys(p.R482C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315073 |
| Start | 181224147:181224147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.148G>A |
| AA Mutation | p.Gly50Arg(p.G50R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315073 |
| Start | 181234295:181234295(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs541488766 |
| CDS Mutation | c.1413C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315073 |
| Start | 181224518:181224518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759985703 |
| CDS Mutation | c.519G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |