Primary Site >> Stomach Cancer
Gene >> THRA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264637 |
| Start | 40077589:40077589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.203T>C |
| AA Mutation | p.Ile68Thr(p.I68T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264637 |
| Start | 40093092:40093092(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199759695 |
| CDS Mutation | c.1183G>A |
| AA Mutation | p.Val395Ile(p.V395I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264637 |
| Start | 40083875:40083875(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.263C>T |
| AA Mutation | p.Thr88Ile(p.T88I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264637 |
| Start | 40089271:40089271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1048G>A |
| AA Mutation | p.Glu350Lys(p.E350K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264637 |
| Start | 40088251:40088251(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.733G>A |
| AA Mutation | p.Glu245Lys(p.E245K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264637 |
| Start | 40088410:40088410(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.892G>A |
| AA Mutation | p.Ala298Thr(p.A298T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264637 |
| Start | 40093334:40093334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1425G>T |
| AA Mutation | p.Glu475Asp(p.E475D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264637 |
| Start | 40088398:40088398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776268798 |
| CDS Mutation | c.880G>A |
| AA Mutation | p.Val294Ile(p.V294I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264637 |
| Start | 40083844:40083844(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.232C>T |
| AA Mutation | p.Arg78Cys(p.R78C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264637 |
| Start | 40088460:40088460(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.942G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264637 |
| Start | 40093319:40093319(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs185488109 |
| CDS Mutation | c.1410G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264637 |
| Start | 40093295:40093295(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149579879 |
| CDS Mutation | c.1386C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264637 |
| Start | 40086778:40086778(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147570693 |
| CDS Mutation | c.648C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |