Primary Site >> Stomach Cancer
Gene >> CYP24A1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216862 |
| Start | 54157453:54157453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs112596218 |
| CDS Mutation | c.1369G>A |
| AA Mutation | p.Val457Ile(p.V457I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216862 |
| Start | 54157273:54157273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1451A>G |
| AA Mutation | p.Asp484Gly(p.D484G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216862 |
| Start | 54162818:54162818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.889C>T |
| AA Mutation | p.Pro297Ser(p.P297S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216862 |
| Start | 54169634:54169634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.598G>C |
| AA Mutation | p.Val200Leu(p.V200L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216862 |
| Start | 54157452:54157452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1370T>C |
| AA Mutation | p.Val457Ala(p.V457A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216862 |
| Start | 54172989:54172989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs114334215 |
| CDS Mutation | c.369C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216862 |
| Start | 54171607:54171607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.513A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216862 |
| Start | 54157520:54157520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1302G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216862 |
| Start | 54162849:54162849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201825042 |
| CDS Mutation | c.858C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216862 |
| Start | 54157194:54157194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150155645 |
| CDS Mutation | c.1530G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216862 |
| Start | 54158155:54158155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200816735 |
| CDS Mutation | c.1167G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000216862 |
| Start | 54158980:54158980(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1134delA |
| AA Mutation | p.Ala379ProfsTer3(p.A379Pfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |