Primary Site >> Liver Cancer
Gene >> MCF2L
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375608 |
| Start | 113064322:113064322(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs563320301 |
| CDS Mutation | c.598G>A |
| AA Mutation | p.Val200Ile(p.V200I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000375608 |
| Start | 113096371:113096371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3166G>A |
| AA Mutation | p.Val1056Ile(p.V1056I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375608 |
| Start | 113096458:113096458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3253G>A |
| AA Mutation | p.Val1085Met(p.V1085M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375608 |
| Start | 113065074:113065074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.835G>A |
| AA Mutation | p.Asp279Asn(p.D279N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375608 |
| Start | 113087264:113087264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2493G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375608 |
| Start | 113076088:113076088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141497667 |
| CDS Mutation | c.1521G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000375608 |
| Start | 113077072:113077072(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1612delC |
| AA Mutation | p.Gln538ArgfsTer17(p.Q538Rfs*17) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |