Primary Site >> Stomach Cancer
Gene >> CYTH1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361101 |
| Start | 78680275:78680275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1033G>A |
| AA Mutation | p.Gly345Arg(p.G345R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361101 |
| Start | 78702584:78702584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.191A>C |
| AA Mutation | p.Lys64Thr(p.K64T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361101 |
| Start | 78680997:78680997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776237586 |
| CDS Mutation | c.937C>T |
| AA Mutation | p.Arg313Trp(p.R313W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361101 |
| Start | 78700393:78700393(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780397308 |
| CDS Mutation | c.488G>A |
| AA Mutation | p.Arg163Gln(p.R163Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361101 |
| Start | 78709681:78709681(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.74G>A |
| AA Mutation | p.Arg25Gln(p.R25Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361101 |
| Start | 78680988:78680988(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.946G>A |
| AA Mutation | p.Glu316Lys(p.E316K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361101 |
| Start | 78700380:78700380(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202032288 |
| CDS Mutation | c.501G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |