Primary Site >> Stomach Cancer
Gene >> MAP3K14
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344686 |
| Start | 45267672:45267672(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2060A>G |
| AA Mutation | p.His687Arg(p.H687R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344686 |
| Start | 45287024:45287024(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs558318157 |
| CDS Mutation | c.559G>A |
| AA Mutation | p.Ala187Thr(p.A187T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344686 |
| Start | 45267705:45267705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759696785 |
| CDS Mutation | c.2027C>T |
| AA Mutation | p.Pro676Leu(p.P676L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344686 |
| Start | 45265204:45265204(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2638C>T |
| AA Mutation | p.Arg880Trp(p.R880W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344686 |
| Start | 45274541:45274541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1343C>T |
| AA Mutation | p.Thr448Ile(p.T448I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344686 |
| Start | 45274470:45274470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1414C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344686 |
| Start | 45271070:45271070(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776444527 |
| CDS Mutation | c.1809G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344686 |
| Start | 45266610:45266610(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775296010 |
| CDS Mutation | c.2505C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344686 |
| Start | 45286545:45286545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1038C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |