Primary Site >> Stomach Cancer
Gene >> KCNJ2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243457 |
| Start | 70175175:70175175(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.136C>T |
| AA Mutation | p.Arg46Cys(p.R46C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243457 |
| Start | 70175430:70175430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.391G>A |
| AA Mutation | p.Ala131Thr(p.A131T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243457 |
| Start | 70176038:70176038(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.999G>T |
| AA Mutation | p.Glu333Asp(p.E333D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243457 |
| Start | 70175571:70175571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771965504 |
| CDS Mutation | c.532G>T |
| AA Mutation | p.Ala178Ser(p.A178S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243457 |
| Start | 70175073:70175073(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.34G>A |
| AA Mutation | p.Val12Ile(p.V12I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243457 |
| Start | 70175512:70175512(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.473T>C |
| AA Mutation | p.Val158Ala(p.V158A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243457 |
| Start | 70175834:70175834(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.795C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243457 |
| Start | 70175921:70175921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751279819 |
| CDS Mutation | c.882C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000243457 |
| Start | 70176246:70176246(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1211delC |
| AA Mutation | p.Pro404LeufsTer3(p.P404Lfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000243457 |
| Start | 70175052:70175052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.13C>T |
| AA Mutation | p.Arg5Ter(p.R5*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |