Primary Site >> Stomach Cancer
Gene >> KCNJ11
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339994 |
| Start | 17387052:17387052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771797701 |
| CDS Mutation | c.1040G>A |
| AA Mutation | p.Arg347His(p.R347H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339994 |
| Start | 17388082:17388082(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs543286136 |
| CDS Mutation | c.10C>T |
| AA Mutation | p.Arg4Cys(p.R4C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339994 |
| Start | 17386969:17386969(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777540229 |
| CDS Mutation | c.1123A>G |
| AA Mutation | p.Met375Val(p.M375V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339994 |
| Start | 17387517:17387517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750778014 |
| CDS Mutation | c.575G>A |
| AA Mutation | p.Arg192His(p.R192H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339994 |
| Start | 17387685:17387685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.407G>A |
| AA Mutation | p.Arg136His(p.R136H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339994 |
| Start | 17387629:17387629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs587783668 |
| CDS Mutation | c.463G>A |
| AA Mutation | p.Val155Met(p.V155M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |