Primary Site >> Stomach Cancer
Gene >> CHAF1A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301280 |
| Start | 4409668:4409668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753346844 |
| CDS Mutation | c.869C>T |
| AA Mutation | p.Pro290Leu(p.P290L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301280 |
| Start | 4422707:4422707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201144491 |
| CDS Mutation | c.1159C>T |
| AA Mutation | p.Arg387Trp(p.R387W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301280 |
| Start | 4428862:4428862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1576T>C |
| AA Mutation | p.Ser526Pro(p.S526P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301280 |
| Start | 4409290:4409290(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.491T>C |
| AA Mutation | p.Ile164Thr(p.I164T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301280 |
| Start | 4432027:4432027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2023G>A |
| AA Mutation | p.Gly675Arg(p.G675R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301280 |
| Start | 4409733:4409733(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.934T>G |
| AA Mutation | p.Phe312Val(p.F312V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301280 |
| Start | 4433535:4433535(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2669G>A |
| AA Mutation | p.Gly890Asp(p.G890D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301280 |
| Start | 4409353:4409353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776340717 |
| CDS Mutation | c.554A>C |
| AA Mutation | p.Glu185Ala(p.E185A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301280 |
| Start | 4422732:4422732(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1184A>C |
| AA Mutation | p.Lys395Thr(p.K395T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301280 |
| Start | 4409431:4409431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769295287 |
| CDS Mutation | c.632C>T |
| AA Mutation | p.Thr211Met(p.T211M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301280 |
| Start | 4433185:4433185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762003232 |
| CDS Mutation | c.2319G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301280 |
| Start | 4430587:4430587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765846530 |
| CDS Mutation | c.1893C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301280 |
| Start | 4433407:4433407(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375315515 |
| CDS Mutation | c.2541G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301280 |
| Start | 4409297:4409297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs546330233 |
| CDS Mutation | c.498C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301280 |
| Start | 4433470:4433470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs564179329 |
| CDS Mutation | c.2604G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |