Primary Site >> Liver Cancer
Gene >> TENM3
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000511685 |
| Start | 182773474:182773474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4895A>G |
| AA Mutation | p.Tyr1632Cys(p.Y1632C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000511685 |
| Start | 182738445:182738445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3280T>C |
| AA Mutation | p.Trp1094Arg(p.W1094R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000511685 |
| Start | 182346731:182346731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.313C>T |
| AA Mutation | p.Leu105Phe(p.L105F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000511685 |
| Start | 182754799:182754799(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4432G>C |
| AA Mutation | p.Ala1478Pro(p.A1478P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000511685 |
| Start | 182680545:182680545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs193270446 |
| CDS Mutation | c.1642G>A |
| AA Mutation | p.Ala548Thr(p.A548T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000511685 |
| Start | 182728968:182728968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2372G>A |
| AA Mutation | p.Gly791Glu(p.G791E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000511685 |
| Start | 182738515:182738515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3350A>G |
| AA Mutation | p.Asp1117Gly(p.D1117G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000511685 |
| Start | 182800094:182800094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762365565 |
| CDS Mutation | c.7843G>A |
| AA Mutation | p.Glu2615Lys(p.E2615K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000511685 |
| Start | 182736965:182736965(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3125G>A |
| AA Mutation | p.Gly1042Glu(p.G1042E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000511685 |
| Start | 182743256:182743256(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3466C>T |
| AA Mutation | p.Arg1156Cys(p.R1156C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000511685 |
| Start | 182800088:182800088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7837C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000511685 |
| Start | 182628723:182628723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.822A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000511685 |
| Start | 182800012:182800012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7761C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000511685 |
| Start | 182800093:182800093(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772839377 |
| CDS Mutation | c.7842C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000511685 |
| Start | 182796692:182796692(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs76754407 |
| CDS Mutation | c.7269A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |