Primary Site >> Stomach Cancer
Gene >> MITF
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000448226 |
| Start | 69964878:69964878(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1211T>C |
| AA Mutation | p.Leu404Pro(p.L404P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000448226 |
| Start | 69937929:69937929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.462A>C |
| AA Mutation | p.Gln154His(p.Q154H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000448226 |
| Start | 69879176:69879176(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.147C>A |
| AA Mutation | p.Ser49Arg(p.S49R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000448226 |
| Start | 69937961:69937961(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.494G>A |
| AA Mutation | p.Gly165Asp(p.G165D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000448226 |
| Start | 69965157:69965157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1490A>G |
| AA Mutation | p.Asp497Gly(p.D497G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000448226 |
| Start | 69939152:69939152(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748492606 |
| CDS Mutation | c.637A>G |
| AA Mutation | p.Asn213Asp(p.N213D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000448226 |
| Start | 69938000:69938000(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.533C>T |
| AA Mutation | p.Pro178Leu(p.P178L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000448226 |
| Start | 69959338:69959338(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762920442 |
| CDS Mutation | c.1097G>A |
| AA Mutation | p.Arg366Gln(p.R366Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000448226 |
| Start | 69879246:69879246(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.217C>T |
| AA Mutation | p.Arg73Cys(p.R73C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000448226 |
| Start | 69959398:69959398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775320252 |
| CDS Mutation | c.1157G>A |
| AA Mutation | p.Arg386Gln(p.R386Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |