Primary Site >> Liver Cancer
Gene >> TNR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263525 |
| Start | 175366036:175366036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2156C>G |
| AA Mutation | p.Thr719Ser(p.T719S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263525 |
| Start | 175391299:175391299(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1496G>A |
| AA Mutation | p.Ser499Asn(p.S499N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263525 |
| Start | 175324468:175324468(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3845A>G |
| AA Mutation | p.Asp1282Gly(p.D1282G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263525 |
| Start | 175365201:175365201(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2396C>G |
| AA Mutation | p.Pro799Arg(p.P799R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263525 |
| Start | 175362740:175362740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745503260 |
| CDS Mutation | c.2777C>T |
| AA Mutation | p.Ala926Val(p.A926V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263525 |
| Start | 175330088:175330088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3779A>G |
| AA Mutation | p.Tyr1260Cys(p.Y1260C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263525 |
| Start | 175396764:175396764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1020G>C |
| AA Mutation | p.Arg340Ser(p.R340S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263525 |
| Start | 175403375:175403375(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756995159 |
| CDS Mutation | c.741C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000263525 |
| Start | 175379673:175379673(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1842G>A |
| AA Mutation | p.Trp614Ter(p.W614*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000263525 |
| Start | 175337570:175337571(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3491dupT |
| AA Mutation | p.Leu1164PhefsTer6(p.L1164Ffs*6) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |