Primary Site >> Stomach Cancer
Gene >> REPIN1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397281 |
| Start | 150371779:150371779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.538G>A |
| AA Mutation | p.Gly180Ser(p.G180S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397281 |
| Start | 150372055:150372055(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.814C>T |
| AA Mutation | p.Arg272Cys(p.R272C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397281 |
| Start | 150371525:150371525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.284G>A |
| AA Mutation | p.Arg95His(p.R95H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397281 |
| Start | 150372005:150372005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.764G>A |
| AA Mutation | p.Arg255His(p.R255H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397281 |
| Start | 150372041:150372041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766431446 |
| CDS Mutation | c.800C>A |
| AA Mutation | p.Pro267His(p.P267H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397281 |
| Start | 150372100:150372100(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.859A>G |
| AA Mutation | p.Thr287Ala(p.T287A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397281 |
| Start | 150372069:150372069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.828G>T |
| AA Mutation | p.Lys276Asn(p.K276N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397281 |
| Start | 150371766:150371766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.525G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397281 |
| Start | 150371638:150371638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.397C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397281 |
| Start | 150371739:150371739(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.498G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397281 |
| Start | 150372687:150372687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377057422 |
| CDS Mutation | c.1446C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |