Primary Site >> Esophagus Cancer
Gene >> MAP3K1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399503 |
| Start | 56881875:56881875(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2675A>G |
| AA Mutation | p.Asn892Ser(p.N892S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399503 |
| Start | 56878983:56878983(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1969A>G |
| AA Mutation | p.Thr657Ala(p.T657A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399503 |
| Start | 56856699:56856699(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.582G>A |
| AA Mutation | p.Met194Ile(p.M194I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399503 |
| Start | 56871966:56871966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1358A>T |
| AA Mutation | p.Glu453Val(p.E453V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399503 |
| Start | 56886012:56886012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756966178 |
| CDS Mutation | c.4063C>T |
| AA Mutation | p.Arg1355Cys(p.R1355C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000399503 |
| Start | 56883586:56883586(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3726A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000399503 |
| Start | 56893554:56893554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760319082 |
| CDS Mutation | c.4413A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000399503 |
| Start | 56884727:56884727(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3883delA |
| AA Mutation | p.Ile1295Ter(p.I1295*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000399503 |
| Start | 56859866:56859870(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.786_790delGAAAT |
| AA Mutation | p.Lys263ArgfsTer36(p.K263Rfs*36) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |