Primary Site >> Esophagus Cancer
Gene >> MAP3K5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359015 |
| Start | 136720574:136720574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.464A>T |
| AA Mutation | p.Glu155Val(p.E155V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359015 |
| Start | 136697296:136697296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.898C>T |
| AA Mutation | p.Arg300Trp(p.R300W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359015 |
| Start | 136651001:136651001(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760179645 |
| CDS Mutation | c.1771G>A |
| AA Mutation | p.Val591Met(p.V591M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359015 |
| Start | 136791919:136791919(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.239G>A |
| AA Mutation | p.Arg80Gln(p.R80Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359015 |
| Start | 136694193:136694193(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1200G>A |
| AA Mutation | p.Met400Ile(p.M400I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359015 |
| Start | 136611337:136611337(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2466C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359015 |
| Start | 136698584:136698584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.711C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359015 |
| Start | 136698662:136698662(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.633C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |