Primary Site >> Stomach Cancer
Gene >> KAT5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377046 |
| Start | 65714618:65714618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.715C>T |
| AA Mutation | p.Arg239Trp(p.R239W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377046 |
| Start | 65712931:65712931(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.158G>A |
| AA Mutation | p.Arg53His(p.R53H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377046 |
| Start | 65718931:65718931(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1384C>G |
| AA Mutation | p.Leu462Val(p.L462V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377046 |
| Start | 65714524:65714524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs554450356 |
| CDS Mutation | c.621G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000377046 |
| Start | 65712982:65712983(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.213dupC |
| AA Mutation | p.Lys72GlnfsTer9(p.K72Qfs*9) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000377046 |
| Start | 65712942:65712943(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.172dupG |
| AA Mutation | p.Val58GlyfsTer4(p.V58Gfs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |