Primary Site >> Stomach Cancer
Gene >> PCCA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376285 |
| Start | 100257646:100257646(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747943045 |
| CDS Mutation | c.689G>A |
| AA Mutation | p.Arg230His(p.R230H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376285 |
| Start | 100209389:100209389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.526G>A |
| AA Mutation | p.Asp176Asn(p.D176N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376285 |
| Start | 100530105:100530105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2126C>A |
| AA Mutation | p.Ser709Tyr(p.S709Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376285 |
| Start | 100301590:100301590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1196G>A |
| AA Mutation | p.Arg399Gln(p.R399Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376285 |
| Start | 100155024:100155024(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.346C>G |
| AA Mutation | p.Pro116Ala(p.P116A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376285 |
| Start | 100425664:100425664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1778C>T |
| AA Mutation | p.Thr593Ile(p.T593I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376285 |
| Start | 100425685:100425685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201702922 |
| CDS Mutation | c.1799C>T |
| AA Mutation | p.Ser600Leu(p.S600L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000376285 |
| Start | 100273198:100273198(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs752570929 |
| CDS Mutation | c.923delT |
| AA Mutation | p.Leu308TrpfsTer14(p.L308Wfs*14) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |