Primary Site >> Stomach Cancer
Gene >> SMUG1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337581 |
| Start | 54182305:54182305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.604G>C |
| AA Mutation | p.Val202Leu(p.V202L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337581 |
| Start | 54182250:54182250(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377053646 |
| CDS Mutation | c.659G>A |
| AA Mutation | p.Arg220Gln(p.R220Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337581 |
| Start | 54182385:54182385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs541683930 |
| CDS Mutation | c.524G>A |
| AA Mutation | p.Arg175His(p.R175H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337581 |
| Start | 54182241:54182241(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771744744 |
| CDS Mutation | c.668G>A |
| AA Mutation | p.Arg223Gln(p.R223Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337581 |
| Start | 54182450:54182450(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.459G>T |
| AA Mutation | p.Glu153Asp(p.E153D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337581 |
| Start | 54183744:54183744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs547497060 |
| CDS Mutation | c.197G>A |
| AA Mutation | p.Arg66His(p.R66H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |