Primary Site >> Stomach Cancer
Gene >> GP5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000401815 |
| Start | 194397387:194397387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.896G>A |
| AA Mutation | p.Arg299His(p.R299H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000401815 |
| Start | 194396620:194396620(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1663A>G |
| AA Mutation | p.Arg555Gly(p.R555G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000401815 |
| Start | 194398008:194398008(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.275G>T |
| AA Mutation | p.Gly92Val(p.G92V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000401815 |
| Start | 194397833:194397833(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.450G>T |
| AA Mutation | p.Glu150Asp(p.E150D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000401815 |
| Start | 194397664:194397664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.619G>A |
| AA Mutation | p.Val207Met(p.V207M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000401815 |
| Start | 194397540:194397540(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.743C>T |
| AA Mutation | p.Thr248Met(p.T248M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000401815 |
| Start | 194397909:194397909(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.374A>G |
| AA Mutation | p.Glu125Gly(p.E125G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000401815 |
| Start | 194398108:194398108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.175G>A |
| AA Mutation | p.Gly59Arg(p.G59R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000401815 |
| Start | 194398218:194398218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779182714 |
| CDS Mutation | c.65C>T |
| AA Mutation | p.Pro22Leu(p.P22L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000401815 |
| Start | 194398161:194398161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.122C>T |
| AA Mutation | p.Ala41Val(p.A41V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000401815 |
| Start | 194397569:194397569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.714C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000401815 |
| Start | 194397650:194397650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.633G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000401815 |
| Start | 194396873:194396873(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs546059539 |
| CDS Mutation | c.1410G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000401815 |
| Start | 194398170:194398170(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs750629635 |
| CDS Mutation | c.113delG |
| AA Mutation | p.Gly38AlafsTer9(p.G38Afs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000401815 |
| Start | 194398271:194398271(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.12delG |
| AA Mutation | p.Thr5LeufsTer42(p.T5Lfs*42) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |