Primary Site >> Stomach Cancer
Gene >> ANXA6
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000354546 |
| Start | 151147884:151147884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.18G>T |
| AA Mutation | p.Gln6His(p.Q6H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354546 |
| Start | 151122946:151122946(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762451507 |
| CDS Mutation | c.1204C>T |
| AA Mutation | p.Arg402Trp(p.R402W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354546 |
| Start | 151136316:151136316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.429G>T |
| AA Mutation | p.Glu143Asp(p.E143D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354546 |
| Start | 151105267:151105267(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1817A>G |
| AA Mutation | p.Asp606Gly(p.D606G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354546 |
| Start | 151129516:151129516(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374143469 |
| CDS Mutation | c.809G>A |
| AA Mutation | p.Arg270Gln(p.R270Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000354546 |
| Start | 151126414:151126414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1044G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000354546 |
| Start | 151109766:151109766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751215230 |
| CDS Mutation | c.1671G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |