Primary Site >> Stomach Cancer
Gene >> NPEPPS
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322157 |
| Start | 47621895:47621895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2735G>T |
| AA Mutation | p.Arg912Leu(p.R912L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322157 |
| Start | 47618407:47618407(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368913646 |
| CDS Mutation | c.2353G>A |
| AA Mutation | p.Ala785Thr(p.A785T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322157 |
| Start | 47585650:47585650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs3968300 |
| CDS Mutation | c.799C>T |
| AA Mutation | p.Arg267Cys(p.R267C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000322157 |
| Start | 47618350:47618350(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2296C>G |
| AA Mutation | p.Leu766Val(p.L766V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322157 |
| Start | 47612540:47612540(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762616490 |
| CDS Mutation | c.2176C>T |
| AA Mutation | p.Arg726Cys(p.R726C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322157 |
| Start | 47605530:47605530(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2073C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322157 |
| Start | 47585694:47585694(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs3968301 |
| CDS Mutation | c.843G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322157 |
| Start | 47545914:47545914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.261G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000322157 |
| Start | 47604038:47604042(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1867_1871delTTCTC |
| AA Mutation | p.Phe623LeufsTer8(p.F623Lfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |