Primary Site >> Stomach Cancer
Gene >> P4HB
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331483 |
| Start | 81846586:81846586(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.899G>A |
| AA Mutation | p.Arg300His(p.R300H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331483 |
| Start | 81846508:81846508(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.977A>G |
| AA Mutation | p.Lys326Arg(p.K326R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331483 |
| Start | 81846536:81846536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.949C>T |
| AA Mutation | p.Leu317Phe(p.L317F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331483 |
| Start | 81855172:81855172(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.594C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331483 |
| Start | 81845207:81845207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1383C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331483 |
| Start | 81845573:81845573(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1347T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331483 |
| Start | 81855492:81855492(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.447G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331483 |
| Start | 81845681:81845681(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200433403 |
| CDS Mutation | c.1239G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000331483 |
| Start | 81845888:81845888(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs773547908 |
| CDS Mutation | c.1160delA |
| AA Mutation | p.Asn387ThrfsTer118(p.N387Tfs*118) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |