Primary Site >> Stomach Cancer
Gene >> ANXA2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396024 |
| Start | 60349082:60349082(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.953A>T |
| AA Mutation | p.Tyr318Phe(p.Y318F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396024 |
| Start | 60364436:60364436(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.236C>T |
| AA Mutation | p.Thr79Ile(p.T79I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396024 |
| Start | 60349184:60349184(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.851G>A |
| AA Mutation | p.Arg284Gln(p.R284Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396024 |
| Start | 60382350:60382350(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.140A>C |
| AA Mutation | p.Lys47Thr(p.K47T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396024 |
| Start | 60349158:60349158(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.877G>A |
| AA Mutation | p.Val293Ile(p.V293I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000396024 |
| Start | 60349186:60349186(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769044999 |
| CDS Mutation | c.849G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000396024 |
| Start | 60364428:60364429(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.240_243dupAAAG |
| AA Mutation | p.Glu82LysfsTer30(p.E82Kfs*30) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |