Primary Site >> Stomach Cancer
Gene >> ARL13B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394222 |
| Start | 94039913:94039913(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.723T>G |
| AA Mutation | p.Asp241Glu(p.D241E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394222 |
| Start | 94039924:94039924(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.734G>A |
| AA Mutation | p.Gly245Asp(p.G245D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394222 |
| Start | 94049478:94049478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1097A>T |
| AA Mutation | p.Asp366Val(p.D366V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394222 |
| Start | 94036648:94036648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.583G>A |
| AA Mutation | p.Asp195Asn(p.D195N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394222 |
| Start | 94049505:94049505(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1124C>T |
| AA Mutation | p.Pro375Leu(p.P375L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394222 |
| Start | 94049500:94049500(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746618270 |
| CDS Mutation | c.1119G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000394222 |
| Start | 94043049:94043049(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.838delA |
| AA Mutation | p.Met280TrpfsTer10(p.M280Wfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000394222 |
| Start | 94036603:94036603(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.543delA |
| AA Mutation | p.Gly182AlafsTer16(p.G182Afs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000394222 |
| Start | 94036735:94036735(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766505681 |
| CDS Mutation | c.670C>T |
| AA Mutation | p.Arg224Ter(p.R224*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000394222 |
| Start | 94036744:94036744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765368269 |
| CDS Mutation | c.679C>T |
| AA Mutation | p.Arg227Ter(p.R227*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |