Primary Site >> Stomach Cancer
Gene >> CCDC62
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253079 |
| Start | 122806185:122806185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1741G>T |
| AA Mutation | p.Gly581Cys(p.G581C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253079 |
| Start | 122813405:122813405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1987G>A |
| AA Mutation | p.Gly663Ser(p.G663S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253079 |
| Start | 122813382:122813382(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1964C>T |
| AA Mutation | p.Pro655Leu(p.P655L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253079 |
| Start | 122781273:122781273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.339G>T |
| AA Mutation | p.Gln113His(p.Q113H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253079 |
| Start | 122801712:122801712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1566A>G |
| AA Mutation | p.Ile522Met(p.I522M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253079 |
| Start | 122806260:122806260(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1816T>G |
| AA Mutation | p.Leu606Val(p.L606V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253079 |
| Start | 122801426:122801426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1280T>C |
| AA Mutation | p.Leu427Ser(p.L427S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000253079 |
| Start | 122801424:122801424(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1278A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000253079 |
| Start | 122785802:122785802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776433830 |
| CDS Mutation | c.480G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |