Primary Site >> Liver Cancer
Gene >> MYT1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328439 |
| Start | 64208411:64208411(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1215G>T |
| AA Mutation | p.Gln405His(p.Q405H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328439 |
| Start | 64208238:64208238(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1042T>A |
| AA Mutation | p.Ser348Thr(p.S348T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328439 |
| Start | 64205699:64205699(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.296T>A |
| AA Mutation | p.Val99Glu(p.V99E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328439 |
| Start | 64213611:64213611(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1595C>A |
| AA Mutation | p.Pro532His(p.P532H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000328439 |
| Start | 64205655:64205655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150526675 |
| CDS Mutation | c.252C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000328439 |
| Start | 64212055:64212055(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1434C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |