Primary Site >> Liver Cancer
Gene >> TRPM7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313478 |
| Start | 50611257:50611257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2116A>G |
| AA Mutation | p.Met706Val(p.M706V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313478 |
| Start | 50609597:50609597(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2564A>T |
| AA Mutation | p.Lys855Ile(p.K855I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313478 |
| Start | 50593710:50593710(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3515A>G |
| AA Mutation | p.Asp1172Gly(p.D1172G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313478 |
| Start | 50592070:50592070(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4165A>G |
| AA Mutation | p.Thr1389Ala(p.T1389A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313478 |
| Start | 50604964:50604964(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2890A>C |
| AA Mutation | p.Ile964Leu(p.I964L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313478 |
| Start | 50592470:50592470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765622293 |
| CDS Mutation | c.3765G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313478 |
| Start | 50575050:50575050(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4821C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313478 |
| Start | 50592335:50592335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3900C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |