Primary Site >> Liver Cancer
Gene >> TRPM8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324695 |
| Start | 233966718:233966718(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1988C>T |
| AA Mutation | p.Ala663Val(p.A663V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324695 |
| Start | 233937460:233937460(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.299C>A |
| AA Mutation | p.Thr100Asn(p.T100N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324695 |
| Start | 233930689:233930689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.139G>A |
| AA Mutation | p.Ala47Thr(p.A47T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324695 |
| Start | 233945988:233945988(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200066478 |
| CDS Mutation | c.832C>T |
| AA Mutation | p.Arg278Trp(p.R278W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324695 |
| Start | 233955202:233955202(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1314G>T |
| AA Mutation | p.Gln438His(p.Q438H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324695 |
| Start | 233969783:233969783(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2114T>A |
| AA Mutation | p.Val705Glu(p.V705E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324695 |
| Start | 233985834:233985834(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2908C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000324695 |
| Start | 233961067:233961067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs187799320 |
| CDS Mutation | c.1653+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000324695 |
| Start | 234008069:234008069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3231-1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |