Primary Site >> Liver Cancer
Gene >> EGF
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265171 |
| Start | 109976178:109976178(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1996A>T |
| AA Mutation | p.Ile666Phe(p.I666F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265171 |
| Start | 109983442:109983442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2392A>G |
| AA Mutation | p.Asn798Asp(p.N798D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265171 |
| Start | 109994793:109994793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2918A>C |
| AA Mutation | p.Asp973Ala(p.D973A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265171 |
| Start | 109964496:109964496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs529423872 |
| CDS Mutation | c.1534G>A |
| AA Mutation | p.Gly512Arg(p.G512R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265171 |
| Start | 109994806:109994806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2931C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265171 |
| Start | 109960907:109960907(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1107T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265171 |
| Start | 109943884:109943884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369090159 |
| CDS Mutation | c.552A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |