Primary Site >> Stomach Cancer
Gene >> YBX3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228251 |
| Start | 10713279:10713279(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760752611 |
| CDS Mutation | c.505C>T |
| AA Mutation | p.Arg169Cys(p.R169C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228251 |
| Start | 10704066:10704066(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745797213 |
| CDS Mutation | c.863G>A |
| AA Mutation | p.Arg288His(p.R288H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228251 |
| Start | 10702024:10702024(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144824557 |
| CDS Mutation | c.989G>A |
| AA Mutation | p.Arg330Gln(p.R330Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228251 |
| Start | 10715710:10715710(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.434T>C |
| AA Mutation | p.Val145Ala(p.V145A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228251 |
| Start | 10702120:10702120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201062345 |
| CDS Mutation | c.893G>A |
| AA Mutation | p.Arg298His(p.R298H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228251 |
| Start | 10709991:10709991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753555662 |
| CDS Mutation | c.697C>T |
| AA Mutation | p.Arg233Trp(p.R233W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228251 |
| Start | 10702027:10702027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.986A>G |
| AA Mutation | p.Tyr329Cys(p.Y329C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228251 |
| Start | 10710014:10710014(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146058214 |
| CDS Mutation | c.674G>A |
| AA Mutation | p.Arg225His(p.R225H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000228251 |
| Start | 10715736:10715736(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.408A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000228251 |
| Start | 10710085:10710085(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750604266 |
| CDS Mutation | c.603C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |