Primary Site >> Stomach Cancer
Gene >> CDC16
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356221 |
| Start | 114246970:114246970(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779267341 |
| CDS Mutation | c.937G>A |
| AA Mutation | p.Gly313Ser(p.G313S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356221 |
| Start | 114265207:114265207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1570G>A |
| AA Mutation | p.Glu524Lys(p.E524K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356221 |
| Start | 114244901:114244901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.779A>G |
| AA Mutation | p.Lys260Arg(p.K260R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356221 |
| Start | 114244951:114244951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.829G>C |
| AA Mutation | p.Glu277Gln(p.E277Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356221 |
| Start | 114246986:114246986(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.953A>G |
| AA Mutation | p.His318Arg(p.H318R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356221 |
| Start | 114262914:114262914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1412C>T |
| AA Mutation | p.Ala471Val(p.A471V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356221 |
| Start | 114239006:114239006(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.218G>A |
| AA Mutation | p.Arg73His(p.R73H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356221 |
| Start | 114257204:114257204(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780976115 |
| CDS Mutation | c.1224C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |