Primary Site >> Liver Cancer
Gene >> MYOF
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359263 |
| Start | 93349839:93349839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4052A>G |
| AA Mutation | p.Asn1351Ser(p.N1351S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359263 |
| Start | 93351258:93351258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs553662967 |
| CDS Mutation | c.3860C>T |
| AA Mutation | p.Ala1287Val(p.A1287V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359263 |
| Start | 93313144:93313144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5765A>T |
| AA Mutation | p.Asp1922Val(p.D1922V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359263 |
| Start | 93356746:93356746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs181998538 |
| CDS Mutation | c.3223C>T |
| AA Mutation | p.Arg1075Cys(p.R1075C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359263 |
| Start | 93374829:93374829(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2235A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000359263 |
| Start | 93401439:93401439(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199504349 |
| CDS Mutation | c.1096C>T |
| AA Mutation | p.Arg366Ter(p.R366*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |