Primary Site >> Stomach Cancer
Gene >> C1orf198
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366663 |
| Start | 230843419:230843419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370439547 |
| CDS Mutation | c.862C>T |
| AA Mutation | p.Pro288Ser(p.P288S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366663 |
| Start | 230843577:230843577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778320924 |
| CDS Mutation | c.704C>T |
| AA Mutation | p.Pro235Leu(p.P235L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366663 |
| Start | 230839890:230839890(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs529493243 |
| CDS Mutation | c.946G>A |
| AA Mutation | p.Val316Ile(p.V316I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366663 |
| Start | 230843767:230843767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.514A>G |
| AA Mutation | p.Arg172Gly(p.R172G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366663 |
| Start | 230868433:230868433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.80G>A |
| AA Mutation | p.Arg27Gln(p.R27Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366663 |
| Start | 230843717:230843717(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775769596 |
| CDS Mutation | c.564G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |