Primary Site >> Esophagus Cancer
Gene >> MAGEC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285879 |
| Start | 141906302:141906302(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.898C>A |
| AA Mutation | p.Gln300Lys(p.Q300K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285879 |
| Start | 141907406:141907406(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2002G>C |
| AA Mutation | p.Glu668Gln(p.E668Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285879 |
| Start | 141908588:141908588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3184T>G |
| AA Mutation | p.Ser1062Ala(p.S1062A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285879 |
| Start | 141907010:141907010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1606C>T |
| AA Mutation | p.Leu536Phe(p.L536F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285879 |
| Start | 141907038:141907038(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1634C>A |
| AA Mutation | p.Pro545His(p.P545H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285879 |
| Start | 141908573:141908573(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141172739 |
| CDS Mutation | c.3169C>T |
| AA Mutation | p.Arg1057Trp(p.R1057W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000285879 |
| Start | 141908414:141908414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3010C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000285879 |
| Start | 141905954:141905954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.550G>T |
| AA Mutation | p.Glu184Ter(p.E184*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000285879 |
| Start | 141907173:141907220(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1778_1825delACTACTTTCCTCAGAGCCCTCCTCAGGGGGAGGACTCCATGTCTCCTC |
| AA Mutation | p.His593_Pro608del(p.H593_P608del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |