Primary Site >> Stomach Cancer
Gene >> TSHR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000541158 |
| Start | 80955768:80955768(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.88G>A |
| AA Mutation | p.Glu30Lys(p.E30K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000541158 |
| Start | 81143116:81143116(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1058A>G |
| AA Mutation | p.Tyr353Cys(p.Y353C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000541158 |
| Start | 81144336:81144336(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2278A>G |
| AA Mutation | p.Met760Val(p.M760V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000541158 |
| Start | 81139774:81139774(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.788T>C |
| AA Mutation | p.Leu263Pro(p.L263P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000541158 |
| Start | 81139737:81139737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.751G>A |
| AA Mutation | p.Glu251Lys(p.E251K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000541158 |
| Start | 81108400:81108400(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.640A>G |
| AA Mutation | p.Thr214Ala(p.T214A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000541158 |
| Start | 81143590:81143590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369995834 |
| CDS Mutation | c.1532C>T |
| AA Mutation | p.Thr511Met(p.T511M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000541158 |
| Start | 81144076:81144076(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2018C>A |
| AA Mutation | p.Ala673Asp(p.A673D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000541158 |
| Start | 81143884:81143884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139352934 |
| CDS Mutation | c.1826G>A |
| AA Mutation | p.Arg609Gln(p.R609Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000541158 |
| Start | 81143424:81143424(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1366C>A |
| AA Mutation | p.Leu456Met(p.L456M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000541158 |
| Start | 81143781:81143781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757875222 |
| CDS Mutation | c.1723G>A |
| AA Mutation | p.Glu575Lys(p.E575K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000541158 |
| Start | 81144182:81144182(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145012289 |
| CDS Mutation | c.2124G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |