Primary Site >> Stomach Cancer
Gene >> RPN2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237530 |
| Start | 37223881:37223881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1096A>G |
| AA Mutation | p.Arg366Gly(p.R366G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237530 |
| Start | 37207385:37207385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.803A>G |
| AA Mutation | p.His268Arg(p.H268R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237530 |
| Start | 37229989:37229989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139589912 |
| CDS Mutation | c.1511A>G |
| AA Mutation | p.Lys504Arg(p.K504R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237530 |
| Start | 37228629:37228629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1379A>C |
| AA Mutation | p.Lys460Thr(p.K460T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237530 |
| Start | 37184293:37184293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201593369 |
| CDS Mutation | c.127C>T |
| AA Mutation | p.Arg43Cys(p.R43C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000237530 |
| Start | 37234064:37234064(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1722T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000237530 |
| Start | 37234028:37234028(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1686G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000237530 |
| Start | 37230014:37230014(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs557396469 |
| CDS Mutation | c.1536G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |