Primary Site >> Stomach Cancer
Gene >> RASSF2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379376 |
| Start | 4790540:4790540(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755156690 |
| CDS Mutation | c.448C>T |
| AA Mutation | p.Arg150Cys(p.R150C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379376 |
| Start | 4790524:4790524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.464T>C |
| AA Mutation | p.Val155Ala(p.V155A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379376 |
| Start | 4792559:4792559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.356A>G |
| AA Mutation | p.Asp119Gly(p.D119G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379376 |
| Start | 4795875:4795875(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.227G>A |
| AA Mutation | p.Arg76His(p.R76H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379376 |
| Start | 4790539:4790539(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145104204 |
| CDS Mutation | c.449G>A |
| AA Mutation | p.Arg150His(p.R150H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379376 |
| Start | 4790536:4790536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145831009 |
| CDS Mutation | c.452G>A |
| AA Mutation | p.Arg151His(p.R151H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379376 |
| Start | 4790517:4790517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762734075 |
| CDS Mutation | c.471G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |