Primary Site >> Stomach Cancer
Gene >> TNFAIP3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237289 |
| Start | 137878550:137878550(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1105G>A |
| AA Mutation | p.Ala369Thr(p.A369T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237289 |
| Start | 137871272:137871272(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.45G>T |
| AA Mutation | p.Met15Ile(p.M15I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237289 |
| Start | 137880107:137880107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs543704449 |
| CDS Mutation | c.1943C>T |
| AA Mutation | p.Ala648Val(p.A648V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237289 |
| Start | 137871408:137871408(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.181C>T |
| AA Mutation | p.Arg61Trp(p.R61W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237289 |
| Start | 137876101:137876101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.740C>A |
| AA Mutation | p.Pro247His(p.P247H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237289 |
| Start | 137874850:137874850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.301G>A |
| AA Mutation | p.Gly101Ser(p.G101S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237289 |
| Start | 137879072:137879072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1627A>G |
| AA Mutation | p.Thr543Ala(p.T543A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237289 |
| Start | 137875013:137875013(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750716064 |
| CDS Mutation | c.464C>T |
| AA Mutation | p.Thr155Met(p.T155M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237289 |
| Start | 137881237:137881237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2291C>T |
| AA Mutation | p.Ala764Val(p.A764V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000237289 |
| Start | 137878612:137878612(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781274783 |
| CDS Mutation | c.1167G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000237289 |
| Start | 137879173:137879173(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140120540 |
| CDS Mutation | c.1728G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000237289 |
| Start | 137875014:137875014(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140424499 |
| CDS Mutation | c.465G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000237289 |
| Start | 137880150:137880150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760291318 |
| CDS Mutation | c.1986C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000237289 |
| Start | 137880108:137880108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758132383 |
| CDS Mutation | c.1944G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |