Primary Site >> Stomach Cancer
Gene >> CCDC116
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292779 |
| Start | 21634368:21634368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764612340 |
| CDS Mutation | c.419C>T |
| AA Mutation | p.Pro140Leu(p.P140L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292779 |
| Start | 21634908:21634908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.845A>C |
| AA Mutation | p.Gln282Pro(p.Q282P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292779 |
| Start | 21636922:21636922(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1694T>C |
| AA Mutation | p.Met565Thr(p.M565T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292779 |
| Start | 21635087:21635087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1024C>A |
| AA Mutation | p.Pro342Thr(p.P342T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292779 |
| Start | 21635097:21635097(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1034A>G |
| AA Mutation | p.Asp345Gly(p.D345G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292779 |
| Start | 21634201:21634201(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.252C>A |
| AA Mutation | p.Asp84Glu(p.D84E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292779 |
| Start | 21634692:21634692(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.629T>C |
| AA Mutation | p.Leu210Pro(p.L210P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292779 |
| Start | 21635002:21635002(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.939G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292779 |
| Start | 21634042:21634042(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.93A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292779 |
| Start | 21634228:21634228(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778183454 |
| CDS Mutation | c.279G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292779 |
| Start | 21634816:21634816(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370484007 |
| CDS Mutation | c.753C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |