Primary Site >> Stomach Cancer
Gene >> TNFRSF11B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297350 |
| Start | 118928807:118928807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.523C>G |
| AA Mutation | p.Gln175Glu(p.Q175E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297350 |
| Start | 118924672:118924672(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370157044 |
| CDS Mutation | c.908C>T |
| AA Mutation | p.Pro303Leu(p.P303L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297350 |
| Start | 118928858:118928858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.472G>A |
| AA Mutation | p.Ala158Thr(p.A158T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297350 |
| Start | 118933021:118933021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs11573906 |
| CDS Mutation | c.310G>A |
| AA Mutation | p.Val104Met(p.V104M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297350 |
| Start | 118924569:118924569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1011C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297350 |
| Start | 118933235:118933235(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs4876870 |
| CDS Mutation | c.96C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297350 |
| Start | 118933097:118933097(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144654126 |
| CDS Mutation | c.234C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297350 |
| Start | 118926600:118926600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.711A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297350 |
| Start | 118926663:118926663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371614996 |
| CDS Mutation | c.648G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297350 |
| Start | 118926612:118926612(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150457771 |
| CDS Mutation | c.699C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |