Primary Site >> Stomach Cancer
Gene >> HIPK2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406875 |
| Start | 139583877:139583877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200640941 |
| CDS Mutation | c.2905G>A |
| AA Mutation | p.Val969Met(p.V969M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406875 |
| Start | 139631203:139631203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756724364 |
| CDS Mutation | c.1309C>T |
| AA Mutation | p.Arg437Cys(p.R437C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406875 |
| Start | 139573175:139573175(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751302512 |
| CDS Mutation | c.3349G>A |
| AA Mutation | p.Val1117Met(p.V1117M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406875 |
| Start | 139716110:139716110(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746489231 |
| CDS Mutation | c.925G>T |
| AA Mutation | p.Ala309Ser(p.A309S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406875 |
| Start | 139583960:139583960(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs550978102 |
| CDS Mutation | c.2822G>A |
| AA Mutation | p.Arg941His(p.R941H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406875 |
| Start | 139600580:139600580(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748728818 |
| CDS Mutation | c.2272G>A |
| AA Mutation | p.Gly758Arg(p.G758R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406875 |
| Start | 139631199:139631199(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1313A>G |
| AA Mutation | p.Asp438Gly(p.D438G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406875 |
| Start | 139716637:139716637(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.398G>A |
| AA Mutation | p.Arg133His(p.R133H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406875 |
| Start | 139573269:139573269(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3255G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406875 |
| Start | 139716855:139716855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772952959 |
| CDS Mutation | c.180G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406875 |
| Start | 139600581:139600581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144631225 |
| CDS Mutation | c.2271C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406875 |
| Start | 139583845:139583845(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2937A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406875 |
| Start | 139583971:139583971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376177257 |
| CDS Mutation | c.2811C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406875 |
| Start | 139716687:139716687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.348T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406875 |
| Start | 139716825:139716825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.210C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406875 |
| Start | 139716606:139716606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs113824554 |
| CDS Mutation | c.429C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000406875 |
| Start | 139716938:139716938(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.97delA |
| AA Mutation | p.Ile33Ter(p.I33*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |