Primary Site >> Stomach Cancer
Gene >> NOD1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222823 |
| Start | 30451514:30451514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1903C>A |
| AA Mutation | p.Leu635Met(p.L635M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222823 |
| Start | 30451315:30451315(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2102A>G |
| AA Mutation | p.His701Arg(p.H701R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222823 |
| Start | 30451568:30451568(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140167031 |
| CDS Mutation | c.1849C>T |
| AA Mutation | p.Arg617Cys(p.R617C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222823 |
| Start | 30452072:30452072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1345C>T |
| AA Mutation | p.Pro449Ser(p.P449S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222823 |
| Start | 30456910:30456910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12G>T |
| AA Mutation | p.Gln4His(p.Q4H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222823 |
| Start | 30452755:30452755(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367963834 |
| CDS Mutation | c.662C>T |
| AA Mutation | p.Thr221Met(p.T221M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222823 |
| Start | 30452300:30452300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1117C>A |
| AA Mutation | p.Arg373Ser(p.R373S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222823 |
| Start | 30452528:30452528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201438430 |
| CDS Mutation | c.889C>T |
| AA Mutation | p.Arg297Cys(p.R297C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000222823 |
| Start | 30451986:30451986(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1431C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000222823 |
| Start | 30425698:30425698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761985703 |
| CDS Mutation | c.2802C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000222823 |
| Start | 30451506:30451506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1911C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000222823 |
| Start | 30455222:30455222(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.291C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000222823 |
| Start | 30452544:30452544(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs555848797 |
| CDS Mutation | c.873G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |