Primary Site >> Stomach Cancer
Gene >> HIC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322941 |
| Start | 2058134:2058134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771684583 |
| CDS Mutation | c.1501G>A |
| AA Mutation | p.Gly501Arg(p.G501R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322941 |
| Start | 2058425:2058425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1792G>A |
| AA Mutation | p.Gly598Ser(p.G598S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322941 |
| Start | 2057999:2057999(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765775523 |
| CDS Mutation | c.1366G>A |
| AA Mutation | p.Val456Met(p.V456M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322941 |
| Start | 2056964:2056964(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.331G>A |
| AA Mutation | p.Glu111Lys(p.E111K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322941 |
| Start | 2057811:2057811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1178G>A |
| AA Mutation | p.Gly393Asp(p.G393D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322941 |
| Start | 2056968:2056968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.335C>T |
| AA Mutation | p.Ala112Val(p.A112V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322941 |
| Start | 2056702:2056702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.69G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322941 |
| Start | 2057995:2057995(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1362G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322941 |
| Start | 2057866:2057866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs556577424 |
| CDS Mutation | c.1233G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322941 |
| Start | 2056334:2056334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.25T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000322941 |
| Start | 2058487:2058521(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1857_1891delCGGCGCGGCCGGGGCGCTGGCGGGCTTGGGGGGGC |
| AA Mutation | p.Gly620ProfsTer160(p.G620Pfs*160) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |