Primary Site >> Stomach Cancer
Gene >> PDIA4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286091 |
| Start | 149012308:149012308(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.667C>T |
| AA Mutation | p.Leu223Phe(p.L223F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286091 |
| Start | 149006034:149006034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1151C>T |
| AA Mutation | p.Ala384Val(p.A384V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286091 |
| Start | 149004174:149004174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748968203 |
| CDS Mutation | c.1558C>T |
| AA Mutation | p.Pro520Ser(p.P520S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286091 |
| Start | 149005902:149005902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1283G>C |
| AA Mutation | p.Arg428Thr(p.R428T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286091 |
| Start | 149003965:149003965(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370731622 |
| CDS Mutation | c.1767C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286091 |
| Start | 149004097:149004097(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768420155 |
| CDS Mutation | c.1635C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000286091 |
| Start | 149019198:149019199(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.270-2dupA |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |