Primary Site >> Stomach Cancer
Gene >> CCDC88C
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389857 |
| Start | 91313430:91313430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372425024 |
| CDS Mutation | c.2386C>T |
| AA Mutation | p.Arg796Cys(p.R796C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389857 |
| Start | 91294308:91294308(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758005836 |
| CDS Mutation | c.3977G>A |
| AA Mutation | p.Arg1326His(p.R1326H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000389857 |
| Start | 91324779:91324779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1342G>T |
| AA Mutation | p.Ala448Ser(p.A448S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389857 |
| Start | 91294211:91294211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4074G>T |
| AA Mutation | p.Glu1358Asp(p.E1358D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389857 |
| Start | 91313435:91313435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2381C>T |
| AA Mutation | p.Ala794Val(p.A794V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389857 |
| Start | 91283353:91283353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375420508 |
| CDS Mutation | c.4606G>A |
| AA Mutation | p.Ala1536Thr(p.A1536T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389857 |
| Start | 91338031:91338031(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1024G>A |
| AA Mutation | p.Val342Met(p.V342M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389857 |
| Start | 91313667:91313667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757785765 |
| CDS Mutation | c.2149C>T |
| AA Mutation | p.Arg717Cys(p.R717C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389857 |
| Start | 91273493:91273493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766112055 |
| CDS Mutation | c.5219C>T |
| AA Mutation | p.Ser1740Leu(p.S1740L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389857 |
| Start | 91291036:91291036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4161A>C |
| AA Mutation | p.Lys1387Asn(p.K1387N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389857 |
| Start | 91340000:91340000(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.508T>C |
| AA Mutation | p.Phe170Leu(p.F170L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389857 |
| Start | 91408730:91408730(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754028369 |
| CDS Mutation | c.199G>A |
| AA Mutation | p.Val67Ile(p.V67I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389857 |
| Start | 91338130:91338130(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767030060 |
| CDS Mutation | c.925C>T |
| AA Mutation | p.Arg309Cys(p.R309C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389857 |
| Start | 91321224:91321224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1423C>A |
| AA Mutation | p.Leu475Ile(p.L475I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389857 |
| Start | 91272799:91272799(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5913G>T |
| AA Mutation | p.Gln1971His(p.Q1971H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389857 |
| Start | 91307183:91307183(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3050G>A |
| AA Mutation | p.Gly1017Glu(p.G1017E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389857 |
| Start | 91303885:91303885(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764238956 |
| CDS Mutation | c.3451G>A |
| AA Mutation | p.Glu1151Lys(p.E1151K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389857 |
| Start | 91321159:91321159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1488C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389857 |
| Start | 91339292:91339292(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.795C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389857 |
| Start | 91313932:91313932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761074410 |
| CDS Mutation | c.1884G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389857 |
| Start | 91339971:91339971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756135471 |
| CDS Mutation | c.537C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389857 |
| Start | 91303787:91303787(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369163210 |
| CDS Mutation | c.3549C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389857 |
| Start | 91408731:91408731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.198C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389857 |
| Start | 91321231:91321231(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1416T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389857 |
| Start | 91314064:91314064(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1752C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389857 |
| Start | 91313884:91313884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375836053 |
| CDS Mutation | c.1932C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |