Primary Site >> Stomach Cancer
Gene >> SLC17A5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355773 |
| Start | 73621868:73621868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.914T>G |
| AA Mutation | p.Phe305Cys(p.F305C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355773 |
| Start | 73641824:73641824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.392G>A |
| AA Mutation | p.Ser131Asn(p.S131N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355773 |
| Start | 73635389:73635389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.812G>C |
| AA Mutation | p.Arg271Thr(p.R271T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355773 |
| Start | 73636668:73636668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.653G>T |
| AA Mutation | p.Gly218Val(p.G218V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355773 |
| Start | 73638456:73638456(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.569C>T |
| AA Mutation | p.Ala190Val(p.A190V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000355773 |
| Start | 73641867:73641868(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.348_349delTT |
| AA Mutation | p.Phe116LeufsTer78(p.F116Lfs*78) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000355773 |
| Start | 73641867:73641867(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs772039085 |
| CDS Mutation | c.349delT |
| AA Mutation | p.Tyr117MetfsTer17(p.Y117Mfs*17) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000355773 |
| Start | 73595158:73595158(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1407delT |
| AA Mutation | p.Phe469LeufsTer33(p.F469Lfs*33) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000355773 |
| Start | 73641811:73641811(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.405delG |
| AA Mutation | p.Met137CysfsTer3(p.M137Cfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |