Primary Site >> Stomach Cancer
Gene >> IFIH1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263642 |
| Start | 162318163:162318163(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747135877 |
| CDS Mutation | c.145A>G |
| AA Mutation | p.Thr49Ala(p.T49A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263642 |
| Start | 162306764:162306764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.714G>T |
| AA Mutation | p.Trp238Cys(p.W238C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263642 |
| Start | 162273919:162273919(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2330A>G |
| AA Mutation | p.Lys777Arg(p.K777R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263642 |
| Start | 162317914:162317914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.394A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263642 |
| Start | 162282573:162282573(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1099C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263642 |
| Start | 162282469:162282469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1203A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000263642 |
| Start | 162278206:162278206(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs753152979 |
| CDS Mutation | c.1764delA |
| AA Mutation | p.Ala589LeufsTer16(p.A589Lfs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000263642 |
| Start | 162276733:162276739(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2252_2258delCCCACCA |
| AA Mutation | p.Ala751ValfsTer2(p.A751Vfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000263642 |
| Start | 162277607:162277607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745937740 |
| CDS Mutation | c.1852C>T |
| AA Mutation | p.Arg618Ter(p.R618*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000263642 |
| Start | 162272378:162272378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747926684 |
| CDS Mutation | c.2464C>T |
| AA Mutation | p.Arg822Ter(p.R822*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000263642 |
| Start | 162278205:162278206(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs553669430 |
| CDS Mutation | c.1764dupA |
| AA Mutation | p.Ala589SerfsTer21(p.A589Sfs*21) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000263642 |
| Start | 162277555:162277560(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1899_1904delGAAAGA |
| AA Mutation | p.Glu633_Lys634del(p.E633_K634del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |