Primary Site >> Liver Cancer
Gene >> HRNR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368801 |
| Start | 152220085:152220085(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1544C>A |
| AA Mutation | p.Ser515Tyr(p.S515Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368801 |
| Start | 152218579:152218579(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765947560 |
| CDS Mutation | c.3050G>C |
| AA Mutation | p.Gly1017Ala(p.G1017A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368801 |
| Start | 152216113:152216113(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5516C>T |
| AA Mutation | p.Ser1839Phe(p.S1839F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368801 |
| Start | 152213161:152213161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8468G>T |
| AA Mutation | p.Ser2823Ile(p.S2823I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368801 |
| Start | 152214697:152214697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6932A>G |
| AA Mutation | p.His2311Arg(p.H2311R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368801 |
| Start | 152214647:152214647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6982A>G |
| AA Mutation | p.Ser2328Gly(p.S2328G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368801 |
| Start | 152219959:152219959(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1670G>C |
| AA Mutation | p.Ser557Thr(p.S557T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368801 |
| Start | 152213713:152213713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7916C>A |
| AA Mutation | p.Ser2639Tyr(p.S2639Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368801 |
| Start | 152214650:152214650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6979A>T |
| AA Mutation | p.Ser2327Cys(p.S2327C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368801 |
| Start | 152219384:152219384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2245T>A |
| AA Mutation | p.Ser749Thr(p.S749T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368801 |
| Start | 152215934:152215934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5695C>A |
| AA Mutation | p.Gln1899Lys(p.Q1899K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368801 |
| Start | 152215520:152215520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753847125 |
| CDS Mutation | c.6109G>A |
| AA Mutation | p.Gly2037Ser(p.G2037S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368801 |
| Start | 152218574:152218574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150117899 |
| CDS Mutation | c.3055G>A |
| AA Mutation | p.Gly1019Arg(p.G1019R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368801 |
| Start | 152220084:152220084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1545C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000368801 |
| Start | 152218907:152218907(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148651006 |
| CDS Mutation | c.2722C>T |
| AA Mutation | p.Arg908Ter(p.R908*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |