Primary Site >> Stomach Cancer
Gene >> ECEL1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304546 |
| Start | 232484523:232484523(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369255583 |
| CDS Mutation | c.1133C>T |
| AA Mutation | p.Ala378Val(p.A378V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304546 |
| Start | 232484149:232484149(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1259C>T |
| AA Mutation | p.Ala420Val(p.A420V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304546 |
| Start | 232481588:232481588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146580059 |
| CDS Mutation | c.1907C>T |
| AA Mutation | p.Thr636Met(p.T636M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304546 |
| Start | 232486245:232486245(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.409C>T |
| AA Mutation | p.Arg137Cys(p.R137C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304546 |
| Start | 232483128:232483128(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1558G>A |
| AA Mutation | p.Asp520Asn(p.D520N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304546 |
| Start | 232481609:232481609(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1886G>T |
| AA Mutation | p.Gly629Val(p.G629V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304546 |
| Start | 232484198:232484198(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs532757890 |
| CDS Mutation | c.1210C>T |
| AA Mutation | p.Arg404Cys(p.R404C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304546 |
| Start | 232486257:232486257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.397G>A |
| AA Mutation | p.Gly133Ser(p.G133S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304546 |
| Start | 232480452:232480452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199696717 |
| CDS Mutation | c.2175G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304546 |
| Start | 232481548:232481548(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1947C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304546 |
| Start | 232486012:232486012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.642C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304546 |
| Start | 232483147:232483147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199916648 |
| CDS Mutation | c.1539G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000304546 |
| Start | 232484803:232484803(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1057delC |
| AA Mutation | p.His353ThrfsTer8(p.H353Tfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000304546 |
| Start | 232486063:232486064(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.590dupG |
| AA Mutation | p.Arg199AlafsTer66(p.R199Afs*66) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000304546 |
| Start | 232484802:232484803(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs762901217 |
| CDS Mutation | c.1057dupC |
| AA Mutation | p.His353ProfsTer59(p.H353Pfs*59) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |