Primary Site >> Stomach Cancer
Gene >> USP22
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261497 |
| Start | 21028553:21028553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761846968 |
| CDS Mutation | c.293G>A |
| AA Mutation | p.Arg98Gln(p.R98Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261497 |
| Start | 21018106:21018106(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.526C>T |
| AA Mutation | p.Arg176Cys(p.R176C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261497 |
| Start | 21017993:21017993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.639G>A |
| AA Mutation | p.Met213Ile(p.M213I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261497 |
| Start | 21004293:21004293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1444A>C |
| AA Mutation | p.Ser482Arg(p.S482R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261497 |
| Start | 21007966:21007966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773331562 |
| CDS Mutation | c.1134C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261497 |
| Start | 21004207:21004207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753832941 |
| CDS Mutation | c.1530C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |