Primary Site >> Stomach Cancer
Gene >> HECA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367658 |
| Start | 139166877:139166877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200188780 |
| CDS Mutation | c.865C>T |
| AA Mutation | p.Arg289Cys(p.R289C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367658 |
| Start | 139167153:139167153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1141C>T |
| AA Mutation | p.Arg381Trp(p.R381W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367658 |
| Start | 139166808:139166808(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.796G>A |
| AA Mutation | p.Gly266Ser(p.G266S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367658 |
| Start | 139167171:139167171(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766148085 |
| CDS Mutation | c.1159G>A |
| AA Mutation | p.Ala387Thr(p.A387T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367658 |
| Start | 139166335:139166335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.323T>C |
| AA Mutation | p.Leu108Pro(p.L108P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367658 |
| Start | 139166491:139166491(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.479G>A |
| AA Mutation | p.Arg160His(p.R160H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367658 |
| Start | 139166851:139166851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.839T>G |
| AA Mutation | p.Leu280Arg(p.L280R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367658 |
| Start | 139166844:139166844(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.832T>C |
| AA Mutation | p.Ser278Pro(p.S278P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367658 |
| Start | 139167259:139167259(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1247G>A |
| AA Mutation | p.Gly416Glu(p.G416E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367658 |
| Start | 139176980:139176980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1507G>A |
| AA Mutation | p.Asp503Asn(p.D503N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367658 |
| Start | 139167111:139167111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767067217 |
| CDS Mutation | c.1099C>T |
| AA Mutation | p.Arg367Cys(p.R367C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367658 |
| Start | 139167107:139167107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774057363 |
| CDS Mutation | c.1095C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367658 |
| Start | 139174509:139174509(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768154483 |
| CDS Mutation | c.1437C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367658 |
| Start | 139167010:139167010(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1004delG |
| AA Mutation | p.Gly335AspfsTer27(p.G335Dfs*27) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367658 |
| Start | 139166871:139166871(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.860delG |
| AA Mutation | p.Gly287AlafsTer12(p.G287Afs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367658 |
| Start | 139167241:139167241(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1229delA |
| AA Mutation | p.Gln410ArgfsTer11(p.Q410Rfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367658 |
| Start | 139167009:139167010(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs771658394 |
| CDS Mutation | c.1004dupG |
| AA Mutation | p.His336ThrfsTer25(p.H336Tfs*25) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |