Primary Site >> Stomach Cancer
Gene >> NPRL3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000611875 |
| Start | 117354:117354(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.340C>A |
| AA Mutation | p.Pro114Thr(p.P114T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000611875 |
| Start | 89754:89754(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751207437 |
| CDS Mutation | c.1310G>A |
| AA Mutation | p.Arg437His(p.R437H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000611875 |
| Start | 88814:88814(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370803087 |
| CDS Mutation | c.1428G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000611875 |
| Start | 110569:110569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759451803 |
| CDS Mutation | c.585G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000611875 |
| Start | 117322:117322(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.372delT |
| AA Mutation | p.Phe124LeufsTer7(p.F124Lfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000611875 |
| Start | 98229:98230(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.839dupC |
| AA Mutation | p.Ala281CysfsTer50(p.A281Cfs*50) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |