Primary Site >> Stomach Cancer
Gene >> TFAP2C
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000201031 |
| Start | 56637732:56637732(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1072C>A |
| AA Mutation | p.Leu358Met(p.L358M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000201031 |
| Start | 56631811:56631811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.541G>A |
| AA Mutation | p.Asp181Asn(p.D181N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000201031 |
| Start | 56631406:56631406(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.250G>A |
| AA Mutation | p.Ala84Thr(p.A84T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000201031 |
| Start | 56631382:56631382(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.226T>C |
| AA Mutation | p.Tyr76His(p.Y76H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000201031 |
| Start | 56631309:56631309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767119816 |
| CDS Mutation | c.153C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000201031 |
| Start | 56636680:56636680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.993A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000201031 |
| Start | 56633514:56633514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769025070 |
| CDS Mutation | c.748C>T |
| AA Mutation | p.Arg250Ter(p.R250*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |