Primary Site >> Stomach Cancer
Gene >> RHPN1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000620174 |
| Start | 143375652:143375652(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764387997 |
| CDS Mutation | c.160G>A |
| AA Mutation | p.Ala54Thr(p.A54T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000620174 |
| Start | 143380739:143380739(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764935123 |
| CDS Mutation | c.1442G>A |
| AA Mutation | p.Arg481His(p.R481H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000620174 |
| Start | 143381827:143381827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746688062 |
| CDS Mutation | c.1731C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000620174 |
| Start | 143379352:143379352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375036009 |
| CDS Mutation | c.789G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000620174 |
| Start | 143376555:143376555(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.207G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000620174 |
| Start | 143381842:143381842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763333163 |
| CDS Mutation | c.1746A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000620174 |
| Start | 143380705:143380705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1408C>T |
| AA Mutation | p.Gln470Ter(p.Q470*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |