Primary Site >> Stomach Cancer
Gene >> KDM7A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397560 |
| Start | 140091977:140091977(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2558T>G |
| AA Mutation | p.Leu853Arg(p.L853R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397560 |
| Start | 140096987:140096987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2077A>C |
| AA Mutation | p.Thr693Pro(p.T693P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000397560 |
| Start | 140126822:140126822(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.703A>T |
| AA Mutation | p.Met235Leu(p.M235L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397560 |
| Start | 140091963:140091963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2572T>C |
| AA Mutation | p.Tyr858His(p.Y858H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397560 |
| Start | 140091183:140091183(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2737C>T |
| AA Mutation | p.Arg913Cys(p.R913C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397560 |
| Start | 140091894:140091894(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758764278 |
| CDS Mutation | c.2641C>T |
| AA Mutation | p.Pro881Ser(p.P881S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397560 |
| Start | 140097560:140097560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148957004 |
| CDS Mutation | c.2001C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397560 |
| Start | 140096562:140096562(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2367G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397560 |
| Start | 140129497:140129497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368809593 |
| CDS Mutation | c.555T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |