Primary Site >> Stomach Cancer
Gene >> NMT1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258960 |
| Start | 45097136:45097136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150418753 |
| CDS Mutation | c.605G>A |
| AA Mutation | p.Arg202Gln(p.R202Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258960 |
| Start | 45098432:45098432(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746537411 |
| CDS Mutation | c.764G>A |
| AA Mutation | p.Arg255His(p.R255H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258960 |
| Start | 45104892:45104892(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1366A>G |
| AA Mutation | p.Met456Val(p.M456V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258960 |
| Start | 45103856:45103856(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755095071 |
| CDS Mutation | c.1312G>A |
| AA Mutation | p.Ala438Thr(p.A438T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000258960 |
| Start | 45103046:45103046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746356993 |
| CDS Mutation | c.1089G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000258960 |
| Start | 45103004:45103004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1047G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000258960 |
| Start | 45099502:45099502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.982C>T |
| AA Mutation | p.Arg328Ter(p.R328*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |