Primary Site >> Stomach Cancer
Gene >> RHOXF2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371388 |
| Start | 120159398:120159398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370729029 |
| CDS Mutation | c.463C>T |
| AA Mutation | p.Arg155Cys(p.R155C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371388 |
| Start | 120159122:120159122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.187G>A |
| AA Mutation | p.Ala63Thr(p.A63T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371388 |
| Start | 120159294:120159294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781886657 |
| CDS Mutation | c.359G>A |
| AA Mutation | p.Arg120His(p.R120H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371388 |
| Start | 120159400:120159400(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.465C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371388 |
| Start | 120159346:120159346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142963365 |
| CDS Mutation | c.411C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371388 |
| Start | 120159157:120159157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782789286 |
| CDS Mutation | c.222C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371388 |
| Start | 120159292:120159292(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782048832 |
| CDS Mutation | c.357G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |