Primary Site >> Stomach Cancer
Gene >> ITCH
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262650 |
| Start | 34477835:34477835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1756G>A |
| AA Mutation | p.Gly586Ser(p.G586S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000262650 |
| Start | 34489386:34489386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2337G>C |
| AA Mutation | p.Glu779Asp(p.E779D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262650 |
| Start | 34507702:34507702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2620C>T |
| AA Mutation | p.Arg874Cys(p.R874C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262650 |
| Start | 34481193:34481193(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2203G>A |
| AA Mutation | p.Glu735Lys(p.E735K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262650 |
| Start | 34408724:34408724(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.144T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262650 |
| Start | 34442232:34442232(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753960712 |
| CDS Mutation | c.1017C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |