Primary Site >> Liver Cancer
Gene >> LRFN2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338305 |
| Start | 40432975:40432975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.139C>A |
| AA Mutation | p.Pro47Thr(p.P47T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338305 |
| Start | 40392652:40392652(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1661T>C |
| AA Mutation | p.Met554Thr(p.M554T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338305 |
| Start | 40392701:40392701(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1612A>G |
| AA Mutation | p.Ile538Val(p.I538V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338305 |
| Start | 40392635:40392635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1678T>A |
| AA Mutation | p.Cys560Ser(p.C560S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338305 |
| Start | 40432068:40432068(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1046C>A |
| AA Mutation | p.Thr349Asn(p.T349N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338305 |
| Start | 40392590:40392590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1723G>A |
| AA Mutation | p.Val575Met(p.V575M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338305 |
| Start | 40432550:40432550(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756661889 |
| CDS Mutation | c.564C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338305 |
| Start | 40392570:40392570(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147506870 |
| CDS Mutation | c.1743C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |