Primary Site >> Stomach Cancer
Gene >> RAD54L
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371975 |
| Start | 46270710:46270710(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369552170 |
| CDS Mutation | c.1094G>A |
| AA Mutation | p.Arg365Gln(p.R365Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371975 |
| Start | 46273450:46273450(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1471G>A |
| AA Mutation | p.Glu491Lys(p.E491K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371975 |
| Start | 46274161:46274161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1634G>A |
| AA Mutation | p.Gly545Asp(p.G545D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371975 |
| Start | 46274556:46274556(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1708A>G |
| AA Mutation | p.Met570Val(p.M570V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371975 |
| Start | 46267522:46267522(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142375065 |
| CDS Mutation | c.955C>T |
| AA Mutation | p.Arg319Trp(p.R319W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371975 |
| Start | 46260818:46260818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149246216 |
| CDS Mutation | c.569C>T |
| AA Mutation | p.Thr190Met(p.T190M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371975 |
| Start | 46278129:46278129(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2091T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371975 |
| Start | 46260855:46260855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.606C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371975 |
| Start | 46278237:46278237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753869856 |
| CDS Mutation | c.2199C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |