Primary Site >> Stomach Cancer
Gene >> MAP3K3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361733 |
| Start | 63632713:63632713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.37G>A |
| AA Mutation | p.Asp13Asn(p.D13N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361733 |
| Start | 63689576:63689576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.904C>A |
| AA Mutation | p.Gln302Lys(p.Q302K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361733 |
| Start | 63667054:63667054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.496T>C |
| AA Mutation | p.Ser166Pro(p.S166P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361733 |
| Start | 63691800:63691800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1412G>A |
| AA Mutation | p.Arg471Gln(p.R471Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361733 |
| Start | 63689577:63689577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.905A>G |
| AA Mutation | p.Gln302Arg(p.Q302R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361733 |
| Start | 63690351:63690351(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763526019 |
| CDS Mutation | c.1151C>T |
| AA Mutation | p.Thr384Met(p.T384M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361733 |
| Start | 63693619:63693619(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757626698 |
| CDS Mutation | c.1723G>A |
| AA Mutation | p.Ala575Thr(p.A575T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361733 |
| Start | 63667032:63667032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200260705 |
| CDS Mutation | c.474C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361733 |
| Start | 63692249:63692249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1482C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361733 |
| Start | 63693618:63693618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754221571 |
| CDS Mutation | c.1722C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |