Primary Site >> Stomach Cancer
Gene >> MAP2K3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342679 |
| Start | 21305073:21305073(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.719T>C |
| AA Mutation | p.Leu240Pro(p.L240P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342679 |
| Start | 21298913:21298913(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.152C>G |
| AA Mutation | p.Thr51Ser(p.T51S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342679 |
| Start | 21312221:21312221(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371545792 |
| CDS Mutation | c.854C>T |
| AA Mutation | p.Pro285Leu(p.P285L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342679 |
| Start | 21304531:21304531(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.674C>T |
| AA Mutation | p.Ala225Val(p.A225V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342679 |
| Start | 21305064:21305064(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.710A>C |
| AA Mutation | p.Asn237Thr(p.N237T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342679 |
| Start | 21298897:21298897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.136T>C |
| AA Mutation | p.Ser46Pro(p.S46P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000342679 |
| Start | 21298887:21298887(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.126G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000342679 |
| Start | 21312231:21312231(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.864G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000342679 |
| Start | 21304463:21304463(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760897275 |
| CDS Mutation | c.606C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000342679 |
| Start | 21303221:21303221(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752706180 |
| CDS Mutation | c.555G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |