Primary Site >> Stomach Cancer
Gene >> HCRTR1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373706 |
| Start | 31625029:31625029(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.998G>A |
| AA Mutation | p.Arg333His(p.R333H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373706 |
| Start | 31621572:31621572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772394538 |
| CDS Mutation | c.718C>T |
| AA Mutation | p.Arg240Cys(p.R240C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373706 |
| Start | 31619584:31619584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.252C>A |
| AA Mutation | p.Phe84Leu(p.F84L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373706 |
| Start | 31626843:31626843(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1141G>T |
| AA Mutation | p.Gly381Cys(p.G381C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373706 |
| Start | 31620980:31620980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199783403 |
| CDS Mutation | c.516G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373706 |
| Start | 31620854:31620854(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.390G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000373706 |
| Start | 31619231:31619231(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs776607312 |
| CDS Mutation | c.44delC |
| AA Mutation | p.Pro15LeufsTer63(p.P15Lfs*63) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |