Primary Site >> Stomach Cancer
Gene >> ERP44
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262455 |
| Start | 100057826:100057826(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.164C>T |
| AA Mutation | p.Ala55Val(p.A55V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262455 |
| Start | 100052527:100052527(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.176G>A |
| AA Mutation | p.Arg59His(p.R59H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000262455 |
| Start | 100007687:100007687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.765A>T |
| AA Mutation | p.Glu255Asp(p.E255D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262455 |
| Start | 100016351:100016351(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.733G>A |
| AA Mutation | p.Val245Ile(p.V245I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262455 |
| Start | 100022153:100022153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.360G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262455 |
| Start | 100020687:100020687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771231030 |
| CDS Mutation | c.516G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262455 |
| Start | 100018301:100018301(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.600delA |
| AA Mutation | p.Lys200AsnfsTer10(p.K200Nfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000262455 |
| Start | 100016348:100016348(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374215522 |
| CDS Mutation | c.736C>T |
| AA Mutation | p.Arg246Ter(p.R246*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000262455 |
| Start | 100007689:100007690(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.763-1_763insTTTATGT |
| AA Mutation | p.Glu255PhefsTer3(p.E255Ffs*3) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |