Primary Site >> Stomach Cancer
Gene >> IDS
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340855 |
| Start | 149482939:149482939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1460T>C |
| AA Mutation | p.Ile487Thr(p.I487T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340855 |
| Start | 149496374:149496374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782286857 |
| CDS Mutation | c.851C>T |
| AA Mutation | p.Pro284Leu(p.P284L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340855 |
| Start | 149505071:149505071(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782815584 |
| CDS Mutation | c.67G>A |
| AA Mutation | p.Ala23Thr(p.A23T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000340855 |
| Start | 149498149:149498149(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201588028 |
| CDS Mutation | c.666C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000340855 |
| Start | 149483034:149483034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1365T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000340855 |
| Start | 149504160:149504160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782183418 |
| CDS Mutation | c.237G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000340855 |
| Start | 149505072:149505072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.66C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000340855 |
| Start | 149486947:149486947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372340411 |
| CDS Mutation | c.1158C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |