Primary Site >> Stomach Cancer
Gene >> IL12RB1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000593993 |
| Start | 18068499:18068499(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199504990 |
| CDS Mutation | c.1217G>T |
| AA Mutation | p.Gly406Val(p.G406V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000593993 |
| Start | 18080910:18080910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.331G>A |
| AA Mutation | p.Val111Ile(p.V111I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000593993 |
| Start | 18066671:18066671(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768241396 |
| CDS Mutation | c.1354G>A |
| AA Mutation | p.Val452Ile(p.V452I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000593993 |
| Start | 18062270:18062270(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1626G>T |
| AA Mutation | p.Gln542His(p.Q542H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000593993 |
| Start | 18069690:18069690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372865962 |
| CDS Mutation | c.1045G>A |
| AA Mutation | p.Val349Ile(p.V349I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000593993 |
| Start | 18068456:18068456(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1260C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000593993 |
| Start | 18072257:18072257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757032676 |
| CDS Mutation | c.876G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000593993 |
| Start | 18072286:18072286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373643598 |
| CDS Mutation | c.847C>T |
| AA Mutation | p.Arg283Ter(p.R283*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |