Primary Site >> Stomach Cancer
Gene >> CDC73
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367435 |
| Start | 193250681:193250681(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1565T>C |
| AA Mutation | p.Met522Thr(p.M522T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367435 |
| Start | 193236264:193236264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1325T>G |
| AA Mutation | p.Val442Gly(p.V442G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367435 |
| Start | 193130208:193130208(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.272G>A |
| AA Mutation | p.Arg91Gln(p.R91Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367435 |
| Start | 193142054:193142054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.717A>C |
| AA Mutation | p.Gln239His(p.Q239H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367435 |
| Start | 193125123:193125123(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.143A>G |
| AA Mutation | p.Glu48Gly(p.E48G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367435 |
| Start | 193138100:193138100(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.439C>T |
| AA Mutation | p.Arg147Cys(p.R147C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367435 |
| Start | 193152426:193152426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.954G>A |
| AA Mutation | p.Met318Ile(p.M318I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367435 |
| Start | 193236262:193236262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747780211 |
| CDS Mutation | c.1323C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |