Primary Site >> Stomach Cancer
Gene >> HIPK3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303296 |
| Start | 33341110:33341110(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140757794 |
| CDS Mutation | c.1756G>A |
| AA Mutation | p.Gly586Arg(p.G586R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303296 |
| Start | 33286832:33286832(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs556300403 |
| CDS Mutation | c.418G>A |
| AA Mutation | p.Ala140Thr(p.A140T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303296 |
| Start | 33347871:33347871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2164A>G |
| AA Mutation | p.Asn722Asp(p.N722D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303296 |
| Start | 33286638:33286638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.224A>G |
| AA Mutation | p.Asn75Ser(p.N75S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303296 |
| Start | 33287006:33287006(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.592G>A |
| AA Mutation | p.Glu198Lys(p.E198K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303296 |
| Start | 33353554:33353554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3634T>C |
| AA Mutation | p.Tyr1212His(p.Y1212H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303296 |
| Start | 33351834:33351834(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3034G>A |
| AA Mutation | p.Ala1012Thr(p.A1012T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303296 |
| Start | 33353536:33353536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3616C>A |
| AA Mutation | p.Pro1206Thr(p.P1206T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303296 |
| Start | 33286686:33286686(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.272C>T |
| AA Mutation | p.Ala91Val(p.A91V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303296 |
| Start | 33287312:33287312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.898C>T |
| AA Mutation | p.Arg300Trp(p.R300W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303296 |
| Start | 33287453:33287453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1039T>G |
| AA Mutation | p.Ser347Ala(p.S347A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303296 |
| Start | 33347880:33347880(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2173A>T |
| AA Mutation | p.Asn725Tyr(p.N725Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000303296 |
| Start | 33286726:33286726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.312G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000303296 |
| Start | 33338837:33338837(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1422A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000303296 |
| Start | 33348798:33348798(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2646C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000303296 |
| Start | 33328603:33328603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370526633 |
| CDS Mutation | c.1191G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000303296 |
| Start | 33286777:33286777(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.367delC |
| AA Mutation | p.Gln123SerfsTer5(p.Q123Sfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000303296 |
| Start | 33286628:33286628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.214C>T |
| AA Mutation | p.Arg72Ter(p.R72*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000303296 |
| Start | 33337146:33337147(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs761758734 |
| CDS Mutation | c.1300dupT |
| AA Mutation | p.Cys434LeufsTer20(p.C434Lfs*20) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |