Primary Site >> Liver Cancer
Gene >> UNC79
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393151 |
| Start | 93688705:93688705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7067C>A |
| AA Mutation | p.Thr2356Asn(p.T2356N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393151 |
| Start | 93622622:93622622(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5389C>A |
| AA Mutation | p.Pro1797Thr(p.P1797T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393151 |
| Start | 93612968:93612968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3926A>T |
| AA Mutation | p.Lys1309Met(p.K1309M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393151 |
| Start | 93586613:93586613(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780979845 |
| CDS Mutation | c.2821G>A |
| AA Mutation | p.Glu941Lys(p.E941K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393151 |
| Start | 93580348:93580348(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2633T>A |
| AA Mutation | p.Leu878Gln(p.L878Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393151 |
| Start | 93706728:93706728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7732C>T |
| AA Mutation | p.Arg2578Cys(p.R2578C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393151 |
| Start | 93572053:93572053(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1915A>T |
| AA Mutation | p.Asn639Tyr(p.N639Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393151 |
| Start | 93621729:93621729(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4496A>G |
| AA Mutation | p.Gln1499Arg(p.Q1499R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393151 |
| Start | 93706741:93706741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7745T>A |
| AA Mutation | p.Ile2582Asn(p.I2582N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393151 |
| Start | 93497253:93497253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.865G>T |
| AA Mutation | p.Ala289Ser(p.A289S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393151 |
| Start | 93622100:93622100(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375712940 |
| CDS Mutation | c.4867A>G |
| AA Mutation | p.Ile1623Val(p.I1623V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393151 |
| Start | 93538147:93538147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1281C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393151 |
| Start | 93673396:93673396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6799C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |