Primary Site >> Stomach Cancer
Gene >> RASSF8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282884 |
| Start | 26064593:26064593(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.199G>T |
| AA Mutation | p.Gly67Trp(p.G67W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282884 |
| Start | 26064905:26064905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146204306 |
| CDS Mutation | c.511C>T |
| AA Mutation | p.Arg171Cys(p.R171C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282884 |
| Start | 26064710:26064710(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.316C>A |
| AA Mutation | p.Leu106Met(p.L106M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282884 |
| Start | 26064713:26064713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.319C>T |
| AA Mutation | p.Pro107Ser(p.P107S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282884 |
| Start | 26064769:26064769(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.375G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000282884 |
| Start | 26064626:26064626(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746592311 |
| CDS Mutation | c.232C>T |
| AA Mutation | p.Arg78Ter(p.R78*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |