Primary Site >> Stomach Cancer
Gene >> CUL4A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375440 |
| Start | 113260623:113260623(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2048G>T |
| AA Mutation | p.Ser683Ile(p.S683I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375440 |
| Start | 113245981:113245981(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1556G>A |
| AA Mutation | p.Gly519Asp(p.G519D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375440 |
| Start | 113245015:113245015(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1400C>T |
| AA Mutation | p.Ala467Val(p.A467V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375440 |
| Start | 113244425:113244425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1244C>T |
| AA Mutation | p.Ser415Leu(p.S415L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375440 |
| Start | 113260675:113260675(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760052887 |
| CDS Mutation | c.2100C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375440 |
| Start | 113245156:113245156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751190555 |
| CDS Mutation | c.1449C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |