Primary Site >> Stomach Cancer
Gene >> ENAH
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366844 |
| Start | 225498358:225498358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1727A>C |
| AA Mutation | p.Glu576Ala(p.E576A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366844 |
| Start | 225519215:225519215(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370738156 |
| CDS Mutation | c.785G>A |
| AA Mutation | p.Arg262His(p.R262H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366844 |
| Start | 225519320:225519320(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.680A>G |
| AA Mutation | p.Gln227Arg(p.Q227R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366844 |
| Start | 225519216:225519216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375992317 |
| CDS Mutation | c.784C>T |
| AA Mutation | p.Arg262Cys(p.R262C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366844 |
| Start | 225514833:225514833(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.981A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000366844 |
| Start | 225567405:225567406(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.13_14dupAG |
| AA Mutation | p.Ser5ArgfsTer10(p.S5Rfs*10) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |