Primary Site >> Stomach Cancer
Gene >> CDC14A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336454 |
| Start | 100390738:100390738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.223A>G |
| AA Mutation | p.Ser75Gly(p.S75G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336454 |
| Start | 100462866:100462866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754924108 |
| CDS Mutation | c.823G>A |
| AA Mutation | p.Ala275Thr(p.A275T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336454 |
| Start | 100498945:100498945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781410426 |
| CDS Mutation | c.1438C>T |
| AA Mutation | p.Arg480Trp(p.R480W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336454 |
| Start | 100377608:100377608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757576834 |
| CDS Mutation | c.203A>G |
| AA Mutation | p.Asn68Ser(p.N68S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336454 |
| Start | 100498195:100498195(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1409C>T |
| AA Mutation | p.Ala470Val(p.A470V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336454 |
| Start | 100462756:100462756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.713C>G |
| AA Mutation | p.Thr238Arg(p.T238R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336454 |
| Start | 100499046:100499046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1539T>G |
| AA Mutation | p.Phe513Leu(p.F513L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336454 |
| Start | 100462749:100462749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.706C>T |
| AA Mutation | p.Arg236Cys(p.R236C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336454 |
| Start | 100499094:100499094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1587T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000336454 |
| Start | 100424281:100424281(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs773911500 |
| CDS Mutation | c.375delC |
| AA Mutation | p.Tyr126IlefsTer64(p.Y126Ifs*64) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000336454 |
| Start | 100468096:100468096(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.977+2T>C |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |