Primary Site >> Liver Cancer
Gene >> RNF213
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000582970 |
| Start | 80345425:80345425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757174029 |
| CDS Mutation | c.7090G>A |
| AA Mutation | p.Asp2364Asn(p.D2364N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000582970 |
| Start | 80390161:80390161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.15435A>C |
| AA Mutation | p.Gln5145His(p.Q5145H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000582970 |
| Start | 80354492:80354492(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10778A>G |
| AA Mutation | p.Gln3593Arg(p.Q3593R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000582970 |
| Start | 80363132:80363132(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144458310 |
| CDS Mutation | c.11386A>G |
| AA Mutation | p.Arg3796Gly(p.R3796G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000582970 |
| Start | 80354557:80354557(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10843C>A |
| AA Mutation | p.Gln3615Lys(p.Q3615K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000582970 |
| Start | 80345896:80345896(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7561A>G |
| AA Mutation | p.Ile2521Val(p.I2521V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000582970 |
| Start | 80295572:80295572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1771T>C |
| AA Mutation | p.Trp591Arg(p.W591R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000582970 |
| Start | 80273404:80273404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.261A>C |
| AA Mutation | p.Glu87Asp(p.E87D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000582970 |
| Start | 80353546:80353546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10458G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000582970 |
| Start | 80344989:80344989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6654T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000582970 |
| Start | 80347623:80347623(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9288A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000582970 |
| Start | 80273406:80273406(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs74367834 |
| CDS Mutation | c.261+2T>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |