Primary Site >> Stomach Cancer
Gene >> NCR2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373089 |
| Start | 41341827:41341827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142832518 |
| CDS Mutation | c.428G>A |
| AA Mutation | p.Arg143His(p.R143H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373089 |
| Start | 41336209:41336209(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.175T>A |
| AA Mutation | p.Ser59Thr(p.S59T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373089 |
| Start | 41341826:41341826(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763283476 |
| CDS Mutation | c.427C>T |
| AA Mutation | p.Arg143Cys(p.R143C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373089 |
| Start | 41336378:41336378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.344C>A |
| AA Mutation | p.Ser115Tyr(p.S115Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373089 |
| Start | 41341813:41341813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.414C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373089 |
| Start | 41342087:41342087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138366454 |
| CDS Mutation | c.582G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained;frameshift_variant |
| Transcription ID | ENST00000373089 |
| Start | 41350788:41350789(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.755_756insATGAGCATGAGGCCTGAAGG |
| AA Mutation | p.Val253Ter(p.V253*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |