Primary Site >> Stomach Cancer
Gene >> TNFRSF19
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382258 |
| Start | 23668982:23668982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1130G>T |
| AA Mutation | p.Arg377Ile(p.R377I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382258 |
| Start | 23659116:23659116(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.512C>T |
| AA Mutation | p.Ala171Val(p.A171V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382258 |
| Start | 23660374:23660374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372905269 |
| CDS Mutation | c.620G>A |
| AA Mutation | p.Arg207Gln(p.R207Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382258 |
| Start | 23660466:23660466(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751349163 |
| CDS Mutation | c.712C>T |
| AA Mutation | p.Arg238Cys(p.R238C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382258 |
| Start | 23615912:23615912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750280848 |
| CDS Mutation | c.226C>T |
| AA Mutation | p.Arg76Trp(p.R76W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382258 |
| Start | 23659107:23659107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.503C>T |
| AA Mutation | p.Thr168Met(p.T168M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382258 |
| Start | 23668889:23668889(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1037C>T |
| AA Mutation | p.Ser346Phe(p.S346F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382258 |
| Start | 23616029:23616029(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781557698 |
| CDS Mutation | c.343G>A |
| AA Mutation | p.Gly115Arg(p.G115R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382258 |
| Start | 23659086:23659086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139502219 |
| CDS Mutation | c.482C>T |
| AA Mutation | p.Thr161Met(p.T161M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382258 |
| Start | 23659144:23659144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765729212 |
| CDS Mutation | c.540C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382258 |
| Start | 23615971:23615971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762063764 |
| CDS Mutation | c.285C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |