Primary Site >> Stomach Cancer
Gene >> GNAT1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000232461 |
| Start | 50194186:50194186(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.673G>A |
| AA Mutation | p.Ala225Thr(p.A225T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000232461 |
| Start | 50193573:50193573(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.359C>T |
| AA Mutation | p.Ser120Leu(p.S120L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000232461 |
| Start | 50194114:50194114(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.601C>T |
| AA Mutation | p.Arg201Cys(p.R201C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000232461 |
| Start | 50193818:50193818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.515G>A |
| AA Mutation | p.Arg172His(p.R172H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000232461 |
| Start | 50193629:50193629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.415G>A |
| AA Mutation | p.Ala139Thr(p.A139T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000232461 |
| Start | 50193655:50193655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.441G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000232461 |
| Start | 50194152:50194152(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.639C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000232461 |
| Start | 50193574:50193574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745403943 |
| CDS Mutation | c.360G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000232461 |
| Start | 50193777:50193777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758882151 |
| CDS Mutation | c.474G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000232461 |
| Start | 50193585:50193596(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.373_384delCGGCTGTGGAAG |
| AA Mutation | p.Arg125_Lys128del(p.R125_K128del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |