Primary Site >> Stomach Cancer
Gene >> P4HA3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331597 |
| Start | 74268199:74268199(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1510G>A |
| AA Mutation | p.Gly504Arg(p.G504R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331597 |
| Start | 74298240:74298240(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.689T>C |
| AA Mutation | p.Leu230Ser(p.L230S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331597 |
| Start | 74298310:74298310(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370320436 |
| CDS Mutation | c.619G>A |
| AA Mutation | p.Ala207Thr(p.A207T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331597 |
| Start | 74285822:74285822(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1097T>C |
| AA Mutation | p.Leu366Pro(p.L366P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331597 |
| Start | 74286286:74286286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.875T>C |
| AA Mutation | p.Ile292Thr(p.I292T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331597 |
| Start | 74279400:74279400(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140613720 |
| CDS Mutation | c.1163G>A |
| AA Mutation | p.Arg388His(p.R388H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331597 |
| Start | 74304367:74304367(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.246T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331597 |
| Start | 74304385:74304385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.228T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331597 |
| Start | 74302465:74302465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.471T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331597 |
| Start | 74304406:74304406(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776974812 |
| CDS Mutation | c.207C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |