Primary Site >> Stomach Cancer
Gene >> AIMP2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000223029 |
| Start | 6023438:6023438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.710T>C |
| AA Mutation | p.Val237Ala(p.V237A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000223029 |
| Start | 6023678:6023678(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.950A>C |
| AA Mutation | p.Lys317Thr(p.K317T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000223029 |
| Start | 6017971:6017971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771380350 |
| CDS Mutation | c.500A>G |
| AA Mutation | p.Lys167Arg(p.K167R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000223029 |
| Start | 6023536:6023536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770771902 |
| CDS Mutation | c.808G>A |
| AA Mutation | p.Ala270Thr(p.A270T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000223029 |
| Start | 6023591:6023591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.863T>G |
| AA Mutation | p.Ile288Ser(p.I288S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000223029 |
| Start | 6009385:6009385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377537932 |
| CDS Mutation | c.22C>T |
| AA Mutation | p.Pro8Ser(p.P8S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000223029 |
| Start | 6023519:6023519(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.791G>T |
| AA Mutation | p.Gly264Val(p.G264V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000223029 |
| Start | 6023610:6023610(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.882A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000223029 |
| Start | 6023436:6023436(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779256399 |
| CDS Mutation | c.708G>A |
| AA Mutation | p.Trp236Ter(p.W236*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |