Primary Site >> Liver Cancer
Gene >> FCRL5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361835 |
| Start | 157524536:157524536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1982T>A |
| AA Mutation | p.Leu661His(p.L661H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361835 |
| Start | 157539258:157539258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1230C>G |
| AA Mutation | p.Ile410Met(p.I410M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000361835 |
| Start | 157544546:157544546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.560A>G |
| AA Mutation | p.Glu187Gly(p.E187G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361835 |
| Start | 157547114:157547114(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.136G>A |
| AA Mutation | p.Gly46Arg(p.G46R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361835 |
| Start | 157518751:157518751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2692A>T |
| AA Mutation | p.Thr898Ser(p.T898S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361835 |
| Start | 157544369:157544369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.737A>T |
| AA Mutation | p.Gln246Leu(p.Q246L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361835 |
| Start | 157527625:157527625(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1952G>T |
| AA Mutation | p.Ser651Ile(p.S651I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361835 |
| Start | 157534823:157534823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1472C>T |
| AA Mutation | p.Thr491Ile(p.T491I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361835 |
| Start | 157518470:157518470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2771A>G |
| AA Mutation | p.Tyr924Cys(p.Y924C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361835 |
| Start | 157524424:157524424(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776474306 |
| CDS Mutation | c.2094C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361835 |
| Start | 157524499:157524499(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143158449 |
| CDS Mutation | c.2019G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |