Primary Site >> Esophagus Cancer
Gene >> KCNJ12
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331718 |
| Start | 21415761:21415761(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs536297311 |
| CDS Mutation | c.419C>T |
| AA Mutation | p.Thr140Met(p.T140M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331718 |
| Start | 21416186:21416186(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782257483 |
| CDS Mutation | c.844G>A |
| AA Mutation | p.Gly282Ser(p.G282S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331718 |
| Start | 21416361:21416361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1019T>G |
| AA Mutation | p.Ile340Ser(p.I340S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331718 |
| Start | 21416439:21416439(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1097A>C |
| AA Mutation | p.Lys366Thr(p.K366T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331718 |
| Start | 21415921:21415921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782637855 |
| CDS Mutation | c.579G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331718 |
| Start | 21415780:21415780(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782723700 |
| CDS Mutation | c.438C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |