Primary Site >> Stomach Cancer
Gene >> PEPD
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000244137 |
| Start | 33511136:33511136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs533996123 |
| CDS Mutation | c.221C>T |
| AA Mutation | p.Ala74Val(p.A74V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000244137 |
| Start | 33490036:33490036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.463G>A |
| AA Mutation | p.Gly155Ser(p.G155S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000244137 |
| Start | 33401802:33401802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370970279 |
| CDS Mutation | c.886G>A |
| AA Mutation | p.Gly296Ser(p.G296S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000244137 |
| Start | 33512697:33512697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61734503 |
| CDS Mutation | c.97C>T |
| AA Mutation | p.Arg33Trp(p.R33W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000244137 |
| Start | 33493329:33493329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373639982 |
| CDS Mutation | c.402C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000244137 |
| Start | 33478054:33478054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759640890 |
| CDS Mutation | c.540C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000244137 |
| Start | 33478087:33478087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377714630 |
| CDS Mutation | c.507C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000244137 |
| Start | 33490052:33490052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375023206 |
| CDS Mutation | c.447C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |