Primary Site >> Stomach Cancer
Gene >> CSNK1E
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359867 |
| Start | 38300814:38300814(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.475G>A |
| AA Mutation | p.Ala159Thr(p.A159T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359867 |
| Start | 38302904:38302904(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.293G>A |
| AA Mutation | p.Arg98His(p.R98H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359867 |
| Start | 38294116:38294116(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1211C>T |
| AA Mutation | p.Ala404Val(p.A404V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359867 |
| Start | 38300756:38300756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.533G>A |
| AA Mutation | p.Arg178His(p.R178H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359867 |
| Start | 38294419:38294419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1001C>T |
| AA Mutation | p.Thr334Met(p.T334M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359867 |
| Start | 38302963:38302963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762754160 |
| CDS Mutation | c.234C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359867 |
| Start | 38303199:38303199(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.126G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359867 |
| Start | 38294166:38294166(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1161C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000359867 |
| Start | 38303183:38303183(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.142delC |
| AA Mutation | p.Gln48SerfsTer11(p.Q48Sfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000359867 |
| Start | 38302963:38302965(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.232_234delAAC |
| AA Mutation | p.Asn78del(p.N78del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_lost |
| Transcription ID | ENST00000359867 |
| Start | 38293289:38293289(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1249T>C |
| AA Mutation | p.Ter417ArgextTer29(p.*417Rext*29) |
| Mutation Classification | Nonstop_Mutation |
| Feature Type | Transcript |