Primary Site >> Stomach Cancer
Gene >> TGM2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361475 |
| Start | 38138302:38138302(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774425047 |
| CDS Mutation | c.1426C>T |
| AA Mutation | p.Arg476Trp(p.R476W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361475 |
| Start | 38142184:38142184(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.875G>A |
| AA Mutation | p.Gly292Asp(p.G292D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361475 |
| Start | 38132458:38132458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1658A>T |
| AA Mutation | p.Asp553Val(p.D553V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361475 |
| Start | 38138332:38138332(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1396G>A |
| AA Mutation | p.Ala466Thr(p.A466T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361475 |
| Start | 38139582:38139582(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1172C>A |
| AA Mutation | p.Pro391His(p.P391H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361475 |
| Start | 38139589:38139589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs41274716 |
| CDS Mutation | c.1165G>A |
| AA Mutation | p.Asp389Asn(p.D389N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361475 |
| Start | 38138218:38138218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1510G>A |
| AA Mutation | p.Val504Ile(p.V504I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361475 |
| Start | 38146765:38146765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142761662 |
| CDS Mutation | c.811C>T |
| AA Mutation | p.Arg271Cys(p.R271C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361475 |
| Start | 38142150:38142150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.909G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361475 |
| Start | 38131164:38131164(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1842T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361475 |
| Start | 38130315:38130315(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370453250 |
| CDS Mutation | c.1968G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361475 |
| Start | 38139587:38139587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377055359 |
| CDS Mutation | c.1167T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |